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	<id>https://www.na-mic.org/w/api.php?action=feedcontributions&amp;feedformat=atom&amp;user=Msabuncu</id>
	<title>NAMIC Wiki - User contributions [en]</title>
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	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:GroupwiseRegistration&amp;diff=42546</id>
		<title>Projects:GroupwiseRegistration</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:GroupwiseRegistration&amp;diff=42546"/>
		<updated>2009-09-10T19:43:05Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; Back to [[NA-MIC_Internal_Collaborations:StructuralImageAnalysis|NA-MIC Collaborations]], [[Algorithm:MIT|MIT Algorithms]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
= Non-rigid Groupwise Registration =&lt;br /&gt;
&lt;br /&gt;
We aim at providing efficient groupwise registration algorithms &lt;br /&gt;
for population analysis of anatomical structures.&lt;br /&gt;
Here we extend a previously demonstrated entropy based groupwise registration method &lt;br /&gt;
to include a free-form deformation model based on B-splines. &lt;br /&gt;
We provide &lt;br /&gt;
an efficient implementation using stochastic gradient descents &lt;br /&gt;
in a multi-resolution setting. &lt;br /&gt;
We demonstrate the method in application to a set of 50 MRI brain scans &lt;br /&gt;
and compare the results to a pairwise approach &lt;br /&gt;
using segmentation labels to evaluate the quality of alignment.&lt;br /&gt;
Our results indicate that increasing the complexity of the deformation model&lt;br /&gt;
improves registration accuracy significantly, especially at cortical regions.&lt;br /&gt;
&lt;br /&gt;
= Description =&lt;br /&gt;
&lt;br /&gt;
We first describe &lt;br /&gt;
the stack entropy cost function and the B-spline based deformation model.&lt;br /&gt;
Then we discuss implementation details. &lt;br /&gt;
Next, we compare groupwise registration to the pairwise method and&lt;br /&gt;
evaluate both methods using label prediction values.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''Objective Function''&lt;br /&gt;
&lt;br /&gt;
[[Image:GroupwiseStackBiModal.PNG|thumb|350px|Figure 1: On the left is shown a stack of images &lt;br /&gt;
and a sample pixel stack around a cortical region. On the left is shown the Gaussian(blue) fittet to &lt;br /&gt;
a real sample from the dataset we used along with the non-parametric density estimate(red). &lt;br /&gt;
Note that the distribution is bi-modal because of white matter-gray matter transaction.]]&lt;br /&gt;
&lt;br /&gt;
In order to align all subjects in the population,&lt;br /&gt;
we consider sum of pixelwise entropies as a joint alignment criterion.&lt;br /&gt;
The justification for this approach is that if the images are aligned properly, &lt;br /&gt;
intensity values at corresponding coordinate locations from all the images &lt;br /&gt;
will form a low entropy distribution.&lt;br /&gt;
This approach does not require the use of a reference subject; all&lt;br /&gt;
subjects are simultenously driven to the common tendency of the population.&lt;br /&gt;
&lt;br /&gt;
We employ a kernel based density estimation scheme to estimate univariate entropies.&lt;br /&gt;
Using the entropy measure we obtain a better treatment of transitions between different&lt;br /&gt;
tissue types, such as gray matter-white matter transitions in the cortical regions&lt;br /&gt;
where intensity distributions can be bi-modal as shown in Figure 1.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''Deformation Model''&lt;br /&gt;
&lt;br /&gt;
[[Image:GroupwiseBspline.png|thumb|350px|Figure 2: An example deformation field. The local neighborhood affecting the deformation is overlayed on the image.]]&lt;br /&gt;
&lt;br /&gt;
For the nonrigid deformation model,&lt;br /&gt;
we define a combined transformation consisting of &lt;br /&gt;
a global and a local component&lt;br /&gt;
&lt;br /&gt;
:&amp;lt;math&amp;gt;&lt;br /&gt;
T(\mathbf{x}) = T_{local}({T_{global}(\mathbf{x})})&lt;br /&gt;
&amp;lt;/math&amp;gt;&lt;br /&gt;
&lt;br /&gt;
where &amp;lt;math&amp;gt;T_{global}&amp;lt;/math&amp;gt; is a twelve parameter affine transform and &lt;br /&gt;
&amp;lt;math&amp;gt;T_{local}&amp;lt;/math&amp;gt; is a deformation model based on B-splines.&lt;br /&gt;
&lt;br /&gt;
The free form deformation can be written as the 3-D tensor product&lt;br /&gt;
of 1-D cubic B-splines.&lt;br /&gt;
&lt;br /&gt;
:&amp;lt;math&amp;gt;&lt;br /&gt;
T_{local}(\mathbf{x}) = \mathbf{x} + \sum_{l=0}^3\sum_{m=0}^3\sum_{n=0}^3 B_l(u)B_m(v)B_n(w) \Phi_{i+l,j+m,k+n}&lt;br /&gt;
&amp;lt;/math&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
		&lt;br /&gt;
where &amp;lt;math&amp;gt;B_l&amp;lt;/math&amp;gt; is &amp;lt;math&amp;gt;l&amp;lt;/math&amp;gt;'th cubic B-spline basis function. &amp;lt;math&amp;gt;(u,v,w)&amp;lt;/math&amp;gt; is the distance &lt;br /&gt;
to &amp;lt;math&amp;gt;(x,y,z)&amp;lt;/math&amp;gt; from the control point &amp;lt;math&amp;gt;\Phi_{i,j,k}&amp;lt;/math&amp;gt; as shown in Figure 2.&lt;br /&gt;
&lt;br /&gt;
The deformation of a given point can be found using only the control points in the neighborhood of the given point. Therefore,&lt;br /&gt;
optimization of the objective function can be implemented efficiently.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''Implementation''&lt;br /&gt;
&lt;br /&gt;
[[Image:GroupwiseIncreasingScale.PNG|thumb|350px|Figure 3: A registration schedule using gradually increasing deformation field complexity. From left to right deformation fields for increasing deformation field complexity. ]]&lt;br /&gt;
&lt;br /&gt;
We provide an efficient optimization scheme by using line search with the gradient descent algorithm.&lt;br /&gt;
For computational efficiency, we employ a stochastic subsampling procedure. &lt;br /&gt;
In each iteration of the algorithm, &lt;br /&gt;
a random subset is drawn from all samples and the objective function is evaluated&lt;br /&gt;
only on this sample set. &lt;br /&gt;
&lt;br /&gt;
To obtain a dense deformation field capturing anatomical variations at different scales,&lt;br /&gt;
we gradually increase the complexity of the deformation field by refining the grid of B-spline control points.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Image:GroupwiseMultiResolution.PNG|thumb|350px|Figure 4: An example showing the multi-resolution scheme. The registration is first performed at a coarse scale by downsampling the input.&lt;br /&gt;
Results from coarser scales are used to initialize&lt;br /&gt;
optimization at finer scales. Also note that the objective function is only evaluated on a small subset of input points. ]]&lt;br /&gt;
&lt;br /&gt;
As in every iterative search algorithm, local minima pose a significant problem. &lt;br /&gt;
To avoid local minima we use a multi-resolution optimization scheme for each resolution level of the deformation field.&lt;br /&gt;
&lt;br /&gt;
We implemented our groupwise registration method in a multi-threaded fashion using Insight Toolkit(ITK)&lt;br /&gt;
and made the implementation publicly available [http://www.na-mic.org/svn/NAMICSandBox/trunk/MultiImageRegistration/ (code)].&lt;br /&gt;
&lt;br /&gt;
''Results''&lt;br /&gt;
&lt;br /&gt;
[[Image:GroupwiseMeanImages.png|thumb|350px|Figure 5:  Central slices of 3D volumes for groupwise registration. Rows show mean and standard deviation images followed by label overlap images for GM, WM and CSF labels. Columns display the results for affine and B-splines with grid spacing 32, 16 and 8 voxels, respectively. ]]&lt;br /&gt;
[[Image:GroupwiseBarsWMGM.png|thumb|350px|Figure 6: GM, WM DICE measures computed for different deformation field resolution levels. Blue bars show the results for groupwise registration and the red bars show the results for registration to the mean setting.]]&lt;br /&gt;
[[Image:GroupwiseBarsManual.png|thumb|350px|Figure 7: DICE measures for manually segmented labels. Bars correspond to the same setting as in figure 6. ]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
We tested the groupwise registration algorithm on a MR brain dataset. &lt;br /&gt;
The dataset consists of 50 MR brain images of three subgroups:&lt;br /&gt;
schizophrenics, affected disorder and normal control patients. &lt;br /&gt;
MR images are T1 scans with 256x256x128 voxels &lt;br /&gt;
and 0.9375x0.9375x1.5 mm&amp;lt;sup&amp;gt;3&amp;lt;/sup&amp;gt; spacing. &lt;br /&gt;
For each image in the dataset, an automatic tissue classification&lt;br /&gt;
was performed, yielding gray matter (GM), white matter (WM) and cerebro-spinal&lt;br /&gt;
fluid (CSF) labels. In addition, manual segmentations of four subcortical regions &lt;br /&gt;
(left and right hippocampus and amygdala) and four cortical regions (left and right superior temporal &lt;br /&gt;
gyrus and para-hippocampus) were available for each MR image.&lt;br /&gt;
&lt;br /&gt;
Increasing the complexity of the deformation model improves the&lt;br /&gt;
accuracy of prediction. An interesting open problem is automatically&lt;br /&gt;
identifying the appropriate deformation complexity before the&lt;br /&gt;
registration overfits and the accuracy of prediction goes down.  We&lt;br /&gt;
also note that the alignment of the subcortical structures is much&lt;br /&gt;
better than that of the cortical regions. It is not surprising as the&lt;br /&gt;
registration algorithm does not use the information about geometry of the cortex&lt;br /&gt;
to optimize the alignment of the cortex. In addition, it has&lt;br /&gt;
been often observed that the cortical structures exhibit higher&lt;br /&gt;
variability across subjects when considered in the 3D volume rather&lt;br /&gt;
than modelled on the surface.&lt;br /&gt;
&lt;br /&gt;
Our experiments highlight the need for further research in developing&lt;br /&gt;
evaluation criteria for image alignment. We used the standard Dice&lt;br /&gt;
measure, but it is not clear that this measurement captures all the&lt;br /&gt;
nuances of the resulting alignment.&lt;br /&gt;
&lt;br /&gt;
Comparing the groupwise registration to the pairwise approach, we&lt;br /&gt;
observe that the sharpness of the mean images and the tissue overlaps&lt;br /&gt;
in Figure 5 look visually similar. From Figures 6 and 7, we note that&lt;br /&gt;
groupwise registration performs slightly better than the pairwise&lt;br /&gt;
setting in most of the cases, especially as we increase the complexity&lt;br /&gt;
of the warp. This suggests that considering the population as a whole&lt;br /&gt;
and registering subjects jointly brings the population into better&lt;br /&gt;
alignment than matching each subject to a mean template&lt;br /&gt;
image. However, the advantage shown here is only slight; more&lt;br /&gt;
comparative studies are needed of the two approaches.&lt;br /&gt;
&lt;br /&gt;
We compare our groupwise algorithm to a pairwise method where we register&lt;br /&gt;
each subject to the mean intensity using sum of square differences.&lt;br /&gt;
During each iteration we consider the mean image as a reference image&lt;br /&gt;
and register&lt;br /&gt;
every subject to the mean image using sum of squared differences. &lt;br /&gt;
After each iteration the mean image is updated and pairwise registrations are performed until convergence.&lt;br /&gt;
&lt;br /&gt;
The images in Figure 5 show central slices of 3D images after registration. &lt;br /&gt;
Visually, mean images get sharper and variance images becomes darker, especially around central ventricles and cortical regions. &lt;br /&gt;
We can observe that anatomical variability at cortical regions causes significant blur for &lt;br /&gt;
GM, WM and CSF structures using affine registration. &lt;br /&gt;
Finer scales of B-spline deformation fields capture a significant part of this anatomical variability and &lt;br /&gt;
the tissue label overlap images get sharper.&lt;br /&gt;
&lt;br /&gt;
=Asymmetric Image-Template Registration=&lt;br /&gt;
&lt;br /&gt;
A natural requirement in pairwise image registration is that the resulting deformation is independent of the order of the images. This constraint is typically achieved via a symmetric cost function and has been shown to reduce the effects of local optima. Consequently, symmetric registration has been successfully applied to pairwise image registration as well as the spatial alignment of individual images with a template. However, recent work has shown that the relationship between &lt;br /&gt;
an image and a template is fundamentally asymmetric. In this work, we develop a method that reconciles the practical advantages of symmetric registration with the asymmetric nature of image-template registration by adding a simple correction factor to the symmetric cost function. We instantiate our model within a log-domain diffeomorphic registration &lt;br /&gt;
framework. Our experiments show exploiting the asymmetry in image-template registration improves alignment in the image coordinates.&lt;br /&gt;
&lt;br /&gt;
= Key Investigators =&lt;br /&gt;
&lt;br /&gt;
* MIT: M.R. Sabuncu, B.T.T. Yeo, K. Van Leemput, S.K. Balci, P. Golland, S. Wells.&lt;br /&gt;
* Harvard: S. Bouix, M.E. Shenton, B. Fischl.&lt;br /&gt;
&lt;br /&gt;
= Publications =&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt;  Asymmetric Image-Template Registration, M.R. Sabuncu, B.T. Thomas Yeo, T. Vercauteren, K. Van Leemput, P. Golland. To appear in Proceedings of the International Conference on Medical Image Computing and Computer Assisted Intervention (MICCAI), 2009&lt;br /&gt;
&lt;br /&gt;
''In Print''&lt;br /&gt;
&lt;br /&gt;
* [http://www.na-mic.org/publications/pages/display?search=Projects%3AGroupwiseRegistration&amp;amp;submit=Search&amp;amp;words=all&amp;amp;title=checked&amp;amp;keywords=checked&amp;amp;authors=checked&amp;amp;abstract=checked&amp;amp;sponsors=checked&amp;amp;searchbytag=checked| NA-MIC Publications Database]&lt;br /&gt;
&lt;br /&gt;
[[Category: Registration]] [[Category:Segmentation]] [[Category:MRI]] [[Category:Schizophrenia]]&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:GroupwiseRegistration&amp;diff=42545</id>
		<title>Projects:GroupwiseRegistration</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:GroupwiseRegistration&amp;diff=42545"/>
		<updated>2009-09-10T19:42:46Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; Back to [[NA-MIC_Internal_Collaborations:StructuralImageAnalysis|NA-MIC Collaborations]], [[Algorithm:MIT|MIT Algorithms]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
= Non-rigid Groupwise Registration =&lt;br /&gt;
&lt;br /&gt;
We aim at providing efficient groupwise registration algorithms &lt;br /&gt;
for population analysis of anatomical structures.&lt;br /&gt;
Here we extend a previously demonstrated entropy based groupwise registration method &lt;br /&gt;
to include a free-form deformation model based on B-splines. &lt;br /&gt;
We provide &lt;br /&gt;
an efficient implementation using stochastic gradient descents &lt;br /&gt;
in a multi-resolution setting. &lt;br /&gt;
We demonstrate the method in application to a set of 50 MRI brain scans &lt;br /&gt;
and compare the results to a pairwise approach &lt;br /&gt;
using segmentation labels to evaluate the quality of alignment.&lt;br /&gt;
Our results indicate that increasing the complexity of the deformation model&lt;br /&gt;
improves registration accuracy significantly, especially at cortical regions.&lt;br /&gt;
&lt;br /&gt;
= Description =&lt;br /&gt;
&lt;br /&gt;
We first describe &lt;br /&gt;
the stack entropy cost function and the B-spline based deformation model.&lt;br /&gt;
Then we discuss implementation details. &lt;br /&gt;
Next, we compare groupwise registration to the pairwise method and&lt;br /&gt;
evaluate both methods using label prediction values.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''Objective Function''&lt;br /&gt;
&lt;br /&gt;
[[Image:GroupwiseStackBiModal.PNG|thumb|350px|Figure 1: On the left is shown a stack of images &lt;br /&gt;
and a sample pixel stack around a cortical region. On the left is shown the Gaussian(blue) fittet to &lt;br /&gt;
a real sample from the dataset we used along with the non-parametric density estimate(red). &lt;br /&gt;
Note that the distribution is bi-modal because of white matter-gray matter transaction.]]&lt;br /&gt;
&lt;br /&gt;
In order to align all subjects in the population,&lt;br /&gt;
we consider sum of pixelwise entropies as a joint alignment criterion.&lt;br /&gt;
The justification for this approach is that if the images are aligned properly, &lt;br /&gt;
intensity values at corresponding coordinate locations from all the images &lt;br /&gt;
will form a low entropy distribution.&lt;br /&gt;
This approach does not require the use of a reference subject; all&lt;br /&gt;
subjects are simultenously driven to the common tendency of the population.&lt;br /&gt;
&lt;br /&gt;
We employ a kernel based density estimation scheme to estimate univariate entropies.&lt;br /&gt;
Using the entropy measure we obtain a better treatment of transitions between different&lt;br /&gt;
tissue types, such as gray matter-white matter transitions in the cortical regions&lt;br /&gt;
where intensity distributions can be bi-modal as shown in Figure 1.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''Deformation Model''&lt;br /&gt;
&lt;br /&gt;
[[Image:GroupwiseBspline.png|thumb|350px|Figure 2: An example deformation field. The local neighborhood affecting the deformation is overlayed on the image.]]&lt;br /&gt;
&lt;br /&gt;
For the nonrigid deformation model,&lt;br /&gt;
we define a combined transformation consisting of &lt;br /&gt;
a global and a local component&lt;br /&gt;
&lt;br /&gt;
:&amp;lt;math&amp;gt;&lt;br /&gt;
T(\mathbf{x}) = T_{local}({T_{global}(\mathbf{x})})&lt;br /&gt;
&amp;lt;/math&amp;gt;&lt;br /&gt;
&lt;br /&gt;
where &amp;lt;math&amp;gt;T_{global}&amp;lt;/math&amp;gt; is a twelve parameter affine transform and &lt;br /&gt;
&amp;lt;math&amp;gt;T_{local}&amp;lt;/math&amp;gt; is a deformation model based on B-splines.&lt;br /&gt;
&lt;br /&gt;
The free form deformation can be written as the 3-D tensor product&lt;br /&gt;
of 1-D cubic B-splines.&lt;br /&gt;
&lt;br /&gt;
:&amp;lt;math&amp;gt;&lt;br /&gt;
T_{local}(\mathbf{x}) = \mathbf{x} + \sum_{l=0}^3\sum_{m=0}^3\sum_{n=0}^3 B_l(u)B_m(v)B_n(w) \Phi_{i+l,j+m,k+n}&lt;br /&gt;
&amp;lt;/math&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
		&lt;br /&gt;
where &amp;lt;math&amp;gt;B_l&amp;lt;/math&amp;gt; is &amp;lt;math&amp;gt;l&amp;lt;/math&amp;gt;'th cubic B-spline basis function. &amp;lt;math&amp;gt;(u,v,w)&amp;lt;/math&amp;gt; is the distance &lt;br /&gt;
to &amp;lt;math&amp;gt;(x,y,z)&amp;lt;/math&amp;gt; from the control point &amp;lt;math&amp;gt;\Phi_{i,j,k}&amp;lt;/math&amp;gt; as shown in Figure 2.&lt;br /&gt;
&lt;br /&gt;
The deformation of a given point can be found using only the control points in the neighborhood of the given point. Therefore,&lt;br /&gt;
optimization of the objective function can be implemented efficiently.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''Implementation''&lt;br /&gt;
&lt;br /&gt;
[[Image:GroupwiseIncreasingScale.PNG|thumb|350px|Figure 3: A registration schedule using gradually increasing deformation field complexity. From left to right deformation fields for increasing deformation field complexity. ]]&lt;br /&gt;
&lt;br /&gt;
We provide an efficient optimization scheme by using line search with the gradient descent algorithm.&lt;br /&gt;
For computational efficiency, we employ a stochastic subsampling procedure. &lt;br /&gt;
In each iteration of the algorithm, &lt;br /&gt;
a random subset is drawn from all samples and the objective function is evaluated&lt;br /&gt;
only on this sample set. &lt;br /&gt;
&lt;br /&gt;
To obtain a dense deformation field capturing anatomical variations at different scales,&lt;br /&gt;
we gradually increase the complexity of the deformation field by refining the grid of B-spline control points.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Image:GroupwiseMultiResolution.PNG|thumb|350px|Figure 4: An example showing the multi-resolution scheme. The registration is first performed at a coarse scale by downsampling the input.&lt;br /&gt;
Results from coarser scales are used to initialize&lt;br /&gt;
optimization at finer scales. Also note that the objective function is only evaluated on a small subset of input points. ]]&lt;br /&gt;
&lt;br /&gt;
As in every iterative search algorithm, local minima pose a significant problem. &lt;br /&gt;
To avoid local minima we use a multi-resolution optimization scheme for each resolution level of the deformation field.&lt;br /&gt;
&lt;br /&gt;
We implemented our groupwise registration method in a multi-threaded fashion using Insight Toolkit(ITK)&lt;br /&gt;
and made the implementation publicly available [http://www.na-mic.org/svn/NAMICSandBox/trunk/MultiImageRegistration/ (code)].&lt;br /&gt;
&lt;br /&gt;
''Results''&lt;br /&gt;
&lt;br /&gt;
[[Image:GroupwiseMeanImages.png|thumb|350px|Figure 5:  Central slices of 3D volumes for groupwise registration. Rows show mean and standard deviation images followed by label overlap images for GM, WM and CSF labels. Columns display the results for affine and B-splines with grid spacing 32, 16 and 8 voxels, respectively. ]]&lt;br /&gt;
[[Image:GroupwiseBarsWMGM.png|thumb|350px|Figure 6: GM, WM DICE measures computed for different deformation field resolution levels. Blue bars show the results for groupwise registration and the red bars show the results for registration to the mean setting.]]&lt;br /&gt;
[[Image:GroupwiseBarsManual.png|thumb|350px|Figure 7: DICE measures for manually segmented labels. Bars correspond to the same setting as in figure 6. ]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
We tested the groupwise registration algorithm on a MR brain dataset. &lt;br /&gt;
The dataset consists of 50 MR brain images of three subgroups:&lt;br /&gt;
schizophrenics, affected disorder and normal control patients. &lt;br /&gt;
MR images are T1 scans with 256x256x128 voxels &lt;br /&gt;
and 0.9375x0.9375x1.5 mm&amp;lt;sup&amp;gt;3&amp;lt;/sup&amp;gt; spacing. &lt;br /&gt;
For each image in the dataset, an automatic tissue classification&lt;br /&gt;
was performed, yielding gray matter (GM), white matter (WM) and cerebro-spinal&lt;br /&gt;
fluid (CSF) labels. In addition, manual segmentations of four subcortical regions &lt;br /&gt;
(left and right hippocampus and amygdala) and four cortical regions (left and right superior temporal &lt;br /&gt;
gyrus and para-hippocampus) were available for each MR image.&lt;br /&gt;
&lt;br /&gt;
Increasing the complexity of the deformation model improves the&lt;br /&gt;
accuracy of prediction. An interesting open problem is automatically&lt;br /&gt;
identifying the appropriate deformation complexity before the&lt;br /&gt;
registration overfits and the accuracy of prediction goes down.  We&lt;br /&gt;
also note that the alignment of the subcortical structures is much&lt;br /&gt;
better than that of the cortical regions. It is not surprising as the&lt;br /&gt;
registration algorithm does not use the information about geometry of the cortex&lt;br /&gt;
to optimize the alignment of the cortex. In addition, it has&lt;br /&gt;
been often observed that the cortical structures exhibit higher&lt;br /&gt;
variability across subjects when considered in the 3D volume rather&lt;br /&gt;
than modelled on the surface.&lt;br /&gt;
&lt;br /&gt;
Our experiments highlight the need for further research in developing&lt;br /&gt;
evaluation criteria for image alignment. We used the standard Dice&lt;br /&gt;
measure, but it is not clear that this measurement captures all the&lt;br /&gt;
nuances of the resulting alignment.&lt;br /&gt;
&lt;br /&gt;
Comparing the groupwise registration to the pairwise approach, we&lt;br /&gt;
observe that the sharpness of the mean images and the tissue overlaps&lt;br /&gt;
in Figure 5 look visually similar. From Figures 6 and 7, we note that&lt;br /&gt;
groupwise registration performs slightly better than the pairwise&lt;br /&gt;
setting in most of the cases, especially as we increase the complexity&lt;br /&gt;
of the warp. This suggests that considering the population as a whole&lt;br /&gt;
and registering subjects jointly brings the population into better&lt;br /&gt;
alignment than matching each subject to a mean template&lt;br /&gt;
image. However, the advantage shown here is only slight; more&lt;br /&gt;
comparative studies are needed of the two approaches.&lt;br /&gt;
&lt;br /&gt;
We compare our groupwise algorithm to a pairwise method where we register&lt;br /&gt;
each subject to the mean intensity using sum of square differences.&lt;br /&gt;
During each iteration we consider the mean image as a reference image&lt;br /&gt;
and register&lt;br /&gt;
every subject to the mean image using sum of squared differences. &lt;br /&gt;
After each iteration the mean image is updated and pairwise registrations are performed until convergence.&lt;br /&gt;
&lt;br /&gt;
The images in Figure 5 show central slices of 3D images after registration. &lt;br /&gt;
Visually, mean images get sharper and variance images becomes darker, especially around central ventricles and cortical regions. &lt;br /&gt;
We can observe that anatomical variability at cortical regions causes significant blur for &lt;br /&gt;
GM, WM and CSF structures using affine registration. &lt;br /&gt;
Finer scales of B-spline deformation fields capture a significant part of this anatomical variability and &lt;br /&gt;
the tissue label overlap images get sharper.&lt;br /&gt;
&lt;br /&gt;
=Asymmetric Image-Template Registration=&lt;br /&gt;
&lt;br /&gt;
A natural requirement in pairwise image registration is that the resulting deformation is independent of the order of the images. This constraint is typically achieved via a symmetric cost function and has been shown to reduce the effects of local optima. Consequently, symmetric registration has been successfully applied to pairwise image registration as well as the spatial alignment of individual images with a template. However, recent work has shown that the relationship between &lt;br /&gt;
an image and a template is fundamentally asymmetric. In this work, we develop a method that reconciles the practical advantages of symmetric registration with the asymmetric nature of image-template registration by adding a simple correction factor to the symmetric cost function. We instantiate our model within a log-domain diffeomorphic registration &lt;br /&gt;
framework. Our experiments show exploiting the asymmetry in image-template registration improves alignment in the image coordinates.&lt;br /&gt;
&lt;br /&gt;
= Key Investigators =&lt;br /&gt;
&lt;br /&gt;
* MIT: M.R. Sabuncu, B.T.T. Yeo, K. Van Leemput, S.K. Balci, P. Golland, S. Wells.&lt;br /&gt;
* Harvard DBP: S. Bouix, M.E. Shenton, B. Fischl.&lt;br /&gt;
&lt;br /&gt;
= Publications =&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt;  Asymmetric Image-Template Registration, M.R. Sabuncu, B.T. Thomas Yeo, T. Vercauteren, K. Van Leemput, P. Golland. To appear in Proceedings of the International Conference on Medical Image Computing and Computer Assisted Intervention (MICCAI), 2009&lt;br /&gt;
&lt;br /&gt;
''In Print''&lt;br /&gt;
&lt;br /&gt;
* [http://www.na-mic.org/publications/pages/display?search=Projects%3AGroupwiseRegistration&amp;amp;submit=Search&amp;amp;words=all&amp;amp;title=checked&amp;amp;keywords=checked&amp;amp;authors=checked&amp;amp;abstract=checked&amp;amp;sponsors=checked&amp;amp;searchbytag=checked| NA-MIC Publications Database]&lt;br /&gt;
&lt;br /&gt;
[[Category: Registration]] [[Category:Segmentation]] [[Category:MRI]] [[Category:Schizophrenia]]&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:GroupwiseRegistration&amp;diff=42544</id>
		<title>Projects:GroupwiseRegistration</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:GroupwiseRegistration&amp;diff=42544"/>
		<updated>2009-09-10T19:41:26Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: /* Asymmetric Image-Template Registration */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; Back to [[NA-MIC_Internal_Collaborations:StructuralImageAnalysis|NA-MIC Collaborations]], [[Algorithm:MIT|MIT Algorithms]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
= Non-rigid Groupwise Registration =&lt;br /&gt;
&lt;br /&gt;
We aim at providing efficient groupwise registration algorithms &lt;br /&gt;
for population analysis of anatomical structures.&lt;br /&gt;
Here we extend a previously demonstrated entropy based groupwise registration method &lt;br /&gt;
to include a free-form deformation model based on B-splines. &lt;br /&gt;
We provide &lt;br /&gt;
an efficient implementation using stochastic gradient descents &lt;br /&gt;
in a multi-resolution setting. &lt;br /&gt;
We demonstrate the method in application to a set of 50 MRI brain scans &lt;br /&gt;
and compare the results to a pairwise approach &lt;br /&gt;
using segmentation labels to evaluate the quality of alignment.&lt;br /&gt;
Our results indicate that increasing the complexity of the deformation model&lt;br /&gt;
improves registration accuracy significantly, especially at cortical regions.&lt;br /&gt;
&lt;br /&gt;
= Description =&lt;br /&gt;
&lt;br /&gt;
We first describe &lt;br /&gt;
the stack entropy cost function and the B-spline based deformation model.&lt;br /&gt;
Then we discuss implementation details. &lt;br /&gt;
Next, we compare groupwise registration to the pairwise method and&lt;br /&gt;
evaluate both methods using label prediction values.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''Objective Function''&lt;br /&gt;
&lt;br /&gt;
[[Image:GroupwiseStackBiModal.PNG|thumb|350px|Figure 1: On the left is shown a stack of images &lt;br /&gt;
and a sample pixel stack around a cortical region. On the left is shown the Gaussian(blue) fittet to &lt;br /&gt;
a real sample from the dataset we used along with the non-parametric density estimate(red). &lt;br /&gt;
Note that the distribution is bi-modal because of white matter-gray matter transaction.]]&lt;br /&gt;
&lt;br /&gt;
In order to align all subjects in the population,&lt;br /&gt;
we consider sum of pixelwise entropies as a joint alignment criterion.&lt;br /&gt;
The justification for this approach is that if the images are aligned properly, &lt;br /&gt;
intensity values at corresponding coordinate locations from all the images &lt;br /&gt;
will form a low entropy distribution.&lt;br /&gt;
This approach does not require the use of a reference subject; all&lt;br /&gt;
subjects are simultenously driven to the common tendency of the population.&lt;br /&gt;
&lt;br /&gt;
We employ a kernel based density estimation scheme to estimate univariate entropies.&lt;br /&gt;
Using the entropy measure we obtain a better treatment of transitions between different&lt;br /&gt;
tissue types, such as gray matter-white matter transitions in the cortical regions&lt;br /&gt;
where intensity distributions can be bi-modal as shown in Figure 1.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''Deformation Model''&lt;br /&gt;
&lt;br /&gt;
[[Image:GroupwiseBspline.png|thumb|350px|Figure 2: An example deformation field. The local neighborhood affecting the deformation is overlayed on the image.]]&lt;br /&gt;
&lt;br /&gt;
For the nonrigid deformation model,&lt;br /&gt;
we define a combined transformation consisting of &lt;br /&gt;
a global and a local component&lt;br /&gt;
&lt;br /&gt;
:&amp;lt;math&amp;gt;&lt;br /&gt;
T(\mathbf{x}) = T_{local}({T_{global}(\mathbf{x})})&lt;br /&gt;
&amp;lt;/math&amp;gt;&lt;br /&gt;
&lt;br /&gt;
where &amp;lt;math&amp;gt;T_{global}&amp;lt;/math&amp;gt; is a twelve parameter affine transform and &lt;br /&gt;
&amp;lt;math&amp;gt;T_{local}&amp;lt;/math&amp;gt; is a deformation model based on B-splines.&lt;br /&gt;
&lt;br /&gt;
The free form deformation can be written as the 3-D tensor product&lt;br /&gt;
of 1-D cubic B-splines.&lt;br /&gt;
&lt;br /&gt;
:&amp;lt;math&amp;gt;&lt;br /&gt;
T_{local}(\mathbf{x}) = \mathbf{x} + \sum_{l=0}^3\sum_{m=0}^3\sum_{n=0}^3 B_l(u)B_m(v)B_n(w) \Phi_{i+l,j+m,k+n}&lt;br /&gt;
&amp;lt;/math&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
		&lt;br /&gt;
where &amp;lt;math&amp;gt;B_l&amp;lt;/math&amp;gt; is &amp;lt;math&amp;gt;l&amp;lt;/math&amp;gt;'th cubic B-spline basis function. &amp;lt;math&amp;gt;(u,v,w)&amp;lt;/math&amp;gt; is the distance &lt;br /&gt;
to &amp;lt;math&amp;gt;(x,y,z)&amp;lt;/math&amp;gt; from the control point &amp;lt;math&amp;gt;\Phi_{i,j,k}&amp;lt;/math&amp;gt; as shown in Figure 2.&lt;br /&gt;
&lt;br /&gt;
The deformation of a given point can be found using only the control points in the neighborhood of the given point. Therefore,&lt;br /&gt;
optimization of the objective function can be implemented efficiently.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''Implementation''&lt;br /&gt;
&lt;br /&gt;
[[Image:GroupwiseIncreasingScale.PNG|thumb|350px|Figure 3: A registration schedule using gradually increasing deformation field complexity. From left to right deformation fields for increasing deformation field complexity. ]]&lt;br /&gt;
&lt;br /&gt;
We provide an efficient optimization scheme by using line search with the gradient descent algorithm.&lt;br /&gt;
For computational efficiency, we employ a stochastic subsampling procedure. &lt;br /&gt;
In each iteration of the algorithm, &lt;br /&gt;
a random subset is drawn from all samples and the objective function is evaluated&lt;br /&gt;
only on this sample set. &lt;br /&gt;
&lt;br /&gt;
To obtain a dense deformation field capturing anatomical variations at different scales,&lt;br /&gt;
we gradually increase the complexity of the deformation field by refining the grid of B-spline control points.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Image:GroupwiseMultiResolution.PNG|thumb|350px|Figure 4: An example showing the multi-resolution scheme. The registration is first performed at a coarse scale by downsampling the input.&lt;br /&gt;
Results from coarser scales are used to initialize&lt;br /&gt;
optimization at finer scales. Also note that the objective function is only evaluated on a small subset of input points. ]]&lt;br /&gt;
&lt;br /&gt;
As in every iterative search algorithm, local minima pose a significant problem. &lt;br /&gt;
To avoid local minima we use a multi-resolution optimization scheme for each resolution level of the deformation field.&lt;br /&gt;
&lt;br /&gt;
We implemented our groupwise registration method in a multi-threaded fashion using Insight Toolkit(ITK)&lt;br /&gt;
and made the implementation publicly available [http://www.na-mic.org/svn/NAMICSandBox/trunk/MultiImageRegistration/ (code)].&lt;br /&gt;
&lt;br /&gt;
''Results''&lt;br /&gt;
&lt;br /&gt;
[[Image:GroupwiseMeanImages.png|thumb|350px|Figure 5:  Central slices of 3D volumes for groupwise registration. Rows show mean and standard deviation images followed by label overlap images for GM, WM and CSF labels. Columns display the results for affine and B-splines with grid spacing 32, 16 and 8 voxels, respectively. ]]&lt;br /&gt;
[[Image:GroupwiseBarsWMGM.png|thumb|350px|Figure 6: GM, WM DICE measures computed for different deformation field resolution levels. Blue bars show the results for groupwise registration and the red bars show the results for registration to the mean setting.]]&lt;br /&gt;
[[Image:GroupwiseBarsManual.png|thumb|350px|Figure 7: DICE measures for manually segmented labels. Bars correspond to the same setting as in figure 6. ]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
We tested the groupwise registration algorithm on a MR brain dataset. &lt;br /&gt;
The dataset consists of 50 MR brain images of three subgroups:&lt;br /&gt;
schizophrenics, affected disorder and normal control patients. &lt;br /&gt;
MR images are T1 scans with 256x256x128 voxels &lt;br /&gt;
and 0.9375x0.9375x1.5 mm&amp;lt;sup&amp;gt;3&amp;lt;/sup&amp;gt; spacing. &lt;br /&gt;
For each image in the dataset, an automatic tissue classification&lt;br /&gt;
was performed, yielding gray matter (GM), white matter (WM) and cerebro-spinal&lt;br /&gt;
fluid (CSF) labels. In addition, manual segmentations of four subcortical regions &lt;br /&gt;
(left and right hippocampus and amygdala) and four cortical regions (left and right superior temporal &lt;br /&gt;
gyrus and para-hippocampus) were available for each MR image.&lt;br /&gt;
&lt;br /&gt;
Increasing the complexity of the deformation model improves the&lt;br /&gt;
accuracy of prediction. An interesting open problem is automatically&lt;br /&gt;
identifying the appropriate deformation complexity before the&lt;br /&gt;
registration overfits and the accuracy of prediction goes down.  We&lt;br /&gt;
also note that the alignment of the subcortical structures is much&lt;br /&gt;
better than that of the cortical regions. It is not surprising as the&lt;br /&gt;
registration algorithm does not use the information about geometry of the cortex&lt;br /&gt;
to optimize the alignment of the cortex. In addition, it has&lt;br /&gt;
been often observed that the cortical structures exhibit higher&lt;br /&gt;
variability across subjects when considered in the 3D volume rather&lt;br /&gt;
than modelled on the surface.&lt;br /&gt;
&lt;br /&gt;
Our experiments highlight the need for further research in developing&lt;br /&gt;
evaluation criteria for image alignment. We used the standard Dice&lt;br /&gt;
measure, but it is not clear that this measurement captures all the&lt;br /&gt;
nuances of the resulting alignment.&lt;br /&gt;
&lt;br /&gt;
Comparing the groupwise registration to the pairwise approach, we&lt;br /&gt;
observe that the sharpness of the mean images and the tissue overlaps&lt;br /&gt;
in Figure 5 look visually similar. From Figures 6 and 7, we note that&lt;br /&gt;
groupwise registration performs slightly better than the pairwise&lt;br /&gt;
setting in most of the cases, especially as we increase the complexity&lt;br /&gt;
of the warp. This suggests that considering the population as a whole&lt;br /&gt;
and registering subjects jointly brings the population into better&lt;br /&gt;
alignment than matching each subject to a mean template&lt;br /&gt;
image. However, the advantage shown here is only slight; more&lt;br /&gt;
comparative studies are needed of the two approaches.&lt;br /&gt;
&lt;br /&gt;
We compare our groupwise algorithm to a pairwise method where we register&lt;br /&gt;
each subject to the mean intensity using sum of square differences.&lt;br /&gt;
During each iteration we consider the mean image as a reference image&lt;br /&gt;
and register&lt;br /&gt;
every subject to the mean image using sum of squared differences. &lt;br /&gt;
After each iteration the mean image is updated and pairwise registrations are performed until convergence.&lt;br /&gt;
&lt;br /&gt;
The images in Figure 5 show central slices of 3D images after registration. &lt;br /&gt;
Visually, mean images get sharper and variance images becomes darker, especially around central ventricles and cortical regions. &lt;br /&gt;
We can observe that anatomical variability at cortical regions causes significant blur for &lt;br /&gt;
GM, WM and CSF structures using affine registration. &lt;br /&gt;
Finer scales of B-spline deformation fields capture a significant part of this anatomical variability and &lt;br /&gt;
the tissue label overlap images get sharper.&lt;br /&gt;
&lt;br /&gt;
=Asymmetric Image-Template Registration=&lt;br /&gt;
&lt;br /&gt;
A natural requirement in pairwise image registration is that the resulting deformation is independent of the order of the images. This constraint is typically achieved via a symmetric cost function and has been shown to reduce the effects of local optima. Consequently, symmetric registration has been successfully applied to pairwise image registration as well as the spatial alignment of individual images with a template. However, recent work has shown that the relationship between &lt;br /&gt;
an image and a template is fundamentally asymmetric. In this work, we develop a method that reconciles the practical advantages of symmetric registration with the asymmetric nature of image-template registration by adding a simple correction factor to the symmetric cost function. We instantiate our model within a log-domain diffeomorphic registration &lt;br /&gt;
framework. Our experiments show exploiting the asymmetry in image-template registration improves alignment in the image coordinates.&lt;br /&gt;
&lt;br /&gt;
= Key Investigators =&lt;br /&gt;
&lt;br /&gt;
* MIT: M.R. Sabuncu, B.T.T. Yeo, K. Van Leemput, S.K. Balci, P. Golland, S. Wells.&lt;br /&gt;
* Harvard DBP: S. Bouix, M.E. Shenton, B. Fischl.&lt;br /&gt;
&lt;br /&gt;
= Publications =&lt;br /&gt;
''In Print''&lt;br /&gt;
&lt;br /&gt;
* [http://www.na-mic.org/publications/pages/display?search=Projects%3AGroupwiseRegistration&amp;amp;submit=Search&amp;amp;words=all&amp;amp;title=checked&amp;amp;keywords=checked&amp;amp;authors=checked&amp;amp;abstract=checked&amp;amp;sponsors=checked&amp;amp;searchbytag=checked| NA-MIC Publications Database]&lt;br /&gt;
&lt;br /&gt;
[[Category: Registration]] [[Category:Segmentation]] [[Category:MRI]] [[Category:Schizophrenia]]&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:GroupwiseRegistration&amp;diff=42543</id>
		<title>Projects:GroupwiseRegistration</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:GroupwiseRegistration&amp;diff=42543"/>
		<updated>2009-09-10T19:41:08Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; Back to [[NA-MIC_Internal_Collaborations:StructuralImageAnalysis|NA-MIC Collaborations]], [[Algorithm:MIT|MIT Algorithms]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
= Non-rigid Groupwise Registration =&lt;br /&gt;
&lt;br /&gt;
We aim at providing efficient groupwise registration algorithms &lt;br /&gt;
for population analysis of anatomical structures.&lt;br /&gt;
Here we extend a previously demonstrated entropy based groupwise registration method &lt;br /&gt;
to include a free-form deformation model based on B-splines. &lt;br /&gt;
We provide &lt;br /&gt;
an efficient implementation using stochastic gradient descents &lt;br /&gt;
in a multi-resolution setting. &lt;br /&gt;
We demonstrate the method in application to a set of 50 MRI brain scans &lt;br /&gt;
and compare the results to a pairwise approach &lt;br /&gt;
using segmentation labels to evaluate the quality of alignment.&lt;br /&gt;
Our results indicate that increasing the complexity of the deformation model&lt;br /&gt;
improves registration accuracy significantly, especially at cortical regions.&lt;br /&gt;
&lt;br /&gt;
= Description =&lt;br /&gt;
&lt;br /&gt;
We first describe &lt;br /&gt;
the stack entropy cost function and the B-spline based deformation model.&lt;br /&gt;
Then we discuss implementation details. &lt;br /&gt;
Next, we compare groupwise registration to the pairwise method and&lt;br /&gt;
evaluate both methods using label prediction values.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''Objective Function''&lt;br /&gt;
&lt;br /&gt;
[[Image:GroupwiseStackBiModal.PNG|thumb|350px|Figure 1: On the left is shown a stack of images &lt;br /&gt;
and a sample pixel stack around a cortical region. On the left is shown the Gaussian(blue) fittet to &lt;br /&gt;
a real sample from the dataset we used along with the non-parametric density estimate(red). &lt;br /&gt;
Note that the distribution is bi-modal because of white matter-gray matter transaction.]]&lt;br /&gt;
&lt;br /&gt;
In order to align all subjects in the population,&lt;br /&gt;
we consider sum of pixelwise entropies as a joint alignment criterion.&lt;br /&gt;
The justification for this approach is that if the images are aligned properly, &lt;br /&gt;
intensity values at corresponding coordinate locations from all the images &lt;br /&gt;
will form a low entropy distribution.&lt;br /&gt;
This approach does not require the use of a reference subject; all&lt;br /&gt;
subjects are simultenously driven to the common tendency of the population.&lt;br /&gt;
&lt;br /&gt;
We employ a kernel based density estimation scheme to estimate univariate entropies.&lt;br /&gt;
Using the entropy measure we obtain a better treatment of transitions between different&lt;br /&gt;
tissue types, such as gray matter-white matter transitions in the cortical regions&lt;br /&gt;
where intensity distributions can be bi-modal as shown in Figure 1.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''Deformation Model''&lt;br /&gt;
&lt;br /&gt;
[[Image:GroupwiseBspline.png|thumb|350px|Figure 2: An example deformation field. The local neighborhood affecting the deformation is overlayed on the image.]]&lt;br /&gt;
&lt;br /&gt;
For the nonrigid deformation model,&lt;br /&gt;
we define a combined transformation consisting of &lt;br /&gt;
a global and a local component&lt;br /&gt;
&lt;br /&gt;
:&amp;lt;math&amp;gt;&lt;br /&gt;
T(\mathbf{x}) = T_{local}({T_{global}(\mathbf{x})})&lt;br /&gt;
&amp;lt;/math&amp;gt;&lt;br /&gt;
&lt;br /&gt;
where &amp;lt;math&amp;gt;T_{global}&amp;lt;/math&amp;gt; is a twelve parameter affine transform and &lt;br /&gt;
&amp;lt;math&amp;gt;T_{local}&amp;lt;/math&amp;gt; is a deformation model based on B-splines.&lt;br /&gt;
&lt;br /&gt;
The free form deformation can be written as the 3-D tensor product&lt;br /&gt;
of 1-D cubic B-splines.&lt;br /&gt;
&lt;br /&gt;
:&amp;lt;math&amp;gt;&lt;br /&gt;
T_{local}(\mathbf{x}) = \mathbf{x} + \sum_{l=0}^3\sum_{m=0}^3\sum_{n=0}^3 B_l(u)B_m(v)B_n(w) \Phi_{i+l,j+m,k+n}&lt;br /&gt;
&amp;lt;/math&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
		&lt;br /&gt;
where &amp;lt;math&amp;gt;B_l&amp;lt;/math&amp;gt; is &amp;lt;math&amp;gt;l&amp;lt;/math&amp;gt;'th cubic B-spline basis function. &amp;lt;math&amp;gt;(u,v,w)&amp;lt;/math&amp;gt; is the distance &lt;br /&gt;
to &amp;lt;math&amp;gt;(x,y,z)&amp;lt;/math&amp;gt; from the control point &amp;lt;math&amp;gt;\Phi_{i,j,k}&amp;lt;/math&amp;gt; as shown in Figure 2.&lt;br /&gt;
&lt;br /&gt;
The deformation of a given point can be found using only the control points in the neighborhood of the given point. Therefore,&lt;br /&gt;
optimization of the objective function can be implemented efficiently.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''Implementation''&lt;br /&gt;
&lt;br /&gt;
[[Image:GroupwiseIncreasingScale.PNG|thumb|350px|Figure 3: A registration schedule using gradually increasing deformation field complexity. From left to right deformation fields for increasing deformation field complexity. ]]&lt;br /&gt;
&lt;br /&gt;
We provide an efficient optimization scheme by using line search with the gradient descent algorithm.&lt;br /&gt;
For computational efficiency, we employ a stochastic subsampling procedure. &lt;br /&gt;
In each iteration of the algorithm, &lt;br /&gt;
a random subset is drawn from all samples and the objective function is evaluated&lt;br /&gt;
only on this sample set. &lt;br /&gt;
&lt;br /&gt;
To obtain a dense deformation field capturing anatomical variations at different scales,&lt;br /&gt;
we gradually increase the complexity of the deformation field by refining the grid of B-spline control points.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Image:GroupwiseMultiResolution.PNG|thumb|350px|Figure 4: An example showing the multi-resolution scheme. The registration is first performed at a coarse scale by downsampling the input.&lt;br /&gt;
Results from coarser scales are used to initialize&lt;br /&gt;
optimization at finer scales. Also note that the objective function is only evaluated on a small subset of input points. ]]&lt;br /&gt;
&lt;br /&gt;
As in every iterative search algorithm, local minima pose a significant problem. &lt;br /&gt;
To avoid local minima we use a multi-resolution optimization scheme for each resolution level of the deformation field.&lt;br /&gt;
&lt;br /&gt;
We implemented our groupwise registration method in a multi-threaded fashion using Insight Toolkit(ITK)&lt;br /&gt;
and made the implementation publicly available [http://www.na-mic.org/svn/NAMICSandBox/trunk/MultiImageRegistration/ (code)].&lt;br /&gt;
&lt;br /&gt;
''Results''&lt;br /&gt;
&lt;br /&gt;
[[Image:GroupwiseMeanImages.png|thumb|350px|Figure 5:  Central slices of 3D volumes for groupwise registration. Rows show mean and standard deviation images followed by label overlap images for GM, WM and CSF labels. Columns display the results for affine and B-splines with grid spacing 32, 16 and 8 voxels, respectively. ]]&lt;br /&gt;
[[Image:GroupwiseBarsWMGM.png|thumb|350px|Figure 6: GM, WM DICE measures computed for different deformation field resolution levels. Blue bars show the results for groupwise registration and the red bars show the results for registration to the mean setting.]]&lt;br /&gt;
[[Image:GroupwiseBarsManual.png|thumb|350px|Figure 7: DICE measures for manually segmented labels. Bars correspond to the same setting as in figure 6. ]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
We tested the groupwise registration algorithm on a MR brain dataset. &lt;br /&gt;
The dataset consists of 50 MR brain images of three subgroups:&lt;br /&gt;
schizophrenics, affected disorder and normal control patients. &lt;br /&gt;
MR images are T1 scans with 256x256x128 voxels &lt;br /&gt;
and 0.9375x0.9375x1.5 mm&amp;lt;sup&amp;gt;3&amp;lt;/sup&amp;gt; spacing. &lt;br /&gt;
For each image in the dataset, an automatic tissue classification&lt;br /&gt;
was performed, yielding gray matter (GM), white matter (WM) and cerebro-spinal&lt;br /&gt;
fluid (CSF) labels. In addition, manual segmentations of four subcortical regions &lt;br /&gt;
(left and right hippocampus and amygdala) and four cortical regions (left and right superior temporal &lt;br /&gt;
gyrus and para-hippocampus) were available for each MR image.&lt;br /&gt;
&lt;br /&gt;
Increasing the complexity of the deformation model improves the&lt;br /&gt;
accuracy of prediction. An interesting open problem is automatically&lt;br /&gt;
identifying the appropriate deformation complexity before the&lt;br /&gt;
registration overfits and the accuracy of prediction goes down.  We&lt;br /&gt;
also note that the alignment of the subcortical structures is much&lt;br /&gt;
better than that of the cortical regions. It is not surprising as the&lt;br /&gt;
registration algorithm does not use the information about geometry of the cortex&lt;br /&gt;
to optimize the alignment of the cortex. In addition, it has&lt;br /&gt;
been often observed that the cortical structures exhibit higher&lt;br /&gt;
variability across subjects when considered in the 3D volume rather&lt;br /&gt;
than modelled on the surface.&lt;br /&gt;
&lt;br /&gt;
Our experiments highlight the need for further research in developing&lt;br /&gt;
evaluation criteria for image alignment. We used the standard Dice&lt;br /&gt;
measure, but it is not clear that this measurement captures all the&lt;br /&gt;
nuances of the resulting alignment.&lt;br /&gt;
&lt;br /&gt;
Comparing the groupwise registration to the pairwise approach, we&lt;br /&gt;
observe that the sharpness of the mean images and the tissue overlaps&lt;br /&gt;
in Figure 5 look visually similar. From Figures 6 and 7, we note that&lt;br /&gt;
groupwise registration performs slightly better than the pairwise&lt;br /&gt;
setting in most of the cases, especially as we increase the complexity&lt;br /&gt;
of the warp. This suggests that considering the population as a whole&lt;br /&gt;
and registering subjects jointly brings the population into better&lt;br /&gt;
alignment than matching each subject to a mean template&lt;br /&gt;
image. However, the advantage shown here is only slight; more&lt;br /&gt;
comparative studies are needed of the two approaches.&lt;br /&gt;
&lt;br /&gt;
We compare our groupwise algorithm to a pairwise method where we register&lt;br /&gt;
each subject to the mean intensity using sum of square differences.&lt;br /&gt;
During each iteration we consider the mean image as a reference image&lt;br /&gt;
and register&lt;br /&gt;
every subject to the mean image using sum of squared differences. &lt;br /&gt;
After each iteration the mean image is updated and pairwise registrations are performed until convergence.&lt;br /&gt;
&lt;br /&gt;
The images in Figure 5 show central slices of 3D images after registration. &lt;br /&gt;
Visually, mean images get sharper and variance images becomes darker, especially around central ventricles and cortical regions. &lt;br /&gt;
We can observe that anatomical variability at cortical regions causes significant blur for &lt;br /&gt;
GM, WM and CSF structures using affine registration. &lt;br /&gt;
Finer scales of B-spline deformation fields capture a significant part of this anatomical variability and &lt;br /&gt;
the tissue label overlap images get sharper.&lt;br /&gt;
&lt;br /&gt;
=Asymmetric Image-Template Registration=&lt;br /&gt;
&lt;br /&gt;
A natural requirement in pairwise image registration is that the resulting deformation is independent of the order of the images. This constraint is typically achieved via a symmetric cost function and has been shown to reduce the effects of local optima. Consequently, symmetric registration has been successfully applied to pairwise image registration as well as the spatial alignment of individual images with a template. However, recent work has shown that the relationship between &lt;br /&gt;
an image and a template is fundamentally asymmetric. In this paper, we develop a method that reconciles the practical advantages of symmetric registration with the asymmetric nature of image-template registration by adding a simple correction factor to the symmetric cost function. We instantiate our model within a log-domain diffeomorphic registration &lt;br /&gt;
framework. Our experiments show exploiting the asymmetry in image-template registration improves alignment in the image coordinates. &lt;br /&gt;
&lt;br /&gt;
= Key Investigators =&lt;br /&gt;
&lt;br /&gt;
* MIT: M.R. Sabuncu, B.T.T. Yeo, K. Van Leemput, S.K. Balci, P. Golland, S. Wells.&lt;br /&gt;
* Harvard DBP: S. Bouix, M.E. Shenton, B. Fischl.&lt;br /&gt;
&lt;br /&gt;
= Publications =&lt;br /&gt;
''In Print''&lt;br /&gt;
&lt;br /&gt;
* [http://www.na-mic.org/publications/pages/display?search=Projects%3AGroupwiseRegistration&amp;amp;submit=Search&amp;amp;words=all&amp;amp;title=checked&amp;amp;keywords=checked&amp;amp;authors=checked&amp;amp;abstract=checked&amp;amp;sponsors=checked&amp;amp;searchbytag=checked| NA-MIC Publications Database]&lt;br /&gt;
&lt;br /&gt;
[[Category: Registration]] [[Category:Segmentation]] [[Category:MRI]] [[Category:Schizophrenia]]&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:GroupwiseRegistration&amp;diff=42541</id>
		<title>Projects:GroupwiseRegistration</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:GroupwiseRegistration&amp;diff=42541"/>
		<updated>2009-09-10T19:40:41Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; Back to [[NA-MIC_Internal_Collaborations:StructuralImageAnalysis|NA-MIC Collaborations]], [[Algorithm:MIT|MIT Algorithms]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
= Non-rigid Groupwise Registration =&lt;br /&gt;
&lt;br /&gt;
We aim at providing efficient groupwise registration algorithms &lt;br /&gt;
for population analysis of anatomical structures.&lt;br /&gt;
Here we extend a previously demonstrated entropy based groupwise registration method &lt;br /&gt;
to include a free-form deformation model based on B-splines. &lt;br /&gt;
We provide &lt;br /&gt;
an efficient implementation using stochastic gradient descents &lt;br /&gt;
in a multi-resolution setting. &lt;br /&gt;
We demonstrate the method in application to a set of 50 MRI brain scans &lt;br /&gt;
and compare the results to a pairwise approach &lt;br /&gt;
using segmentation labels to evaluate the quality of alignment.&lt;br /&gt;
Our results indicate that increasing the complexity of the deformation model&lt;br /&gt;
improves registration accuracy significantly, especially at cortical regions.&lt;br /&gt;
&lt;br /&gt;
= Description =&lt;br /&gt;
&lt;br /&gt;
We first describe &lt;br /&gt;
the stack entropy cost function and the B-spline based deformation model.&lt;br /&gt;
Then we discuss implementation details. &lt;br /&gt;
Next, we compare groupwise registration to the pairwise method and&lt;br /&gt;
evaluate both methods using label prediction values.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''Objective Function''&lt;br /&gt;
&lt;br /&gt;
[[Image:GroupwiseStackBiModal.PNG|thumb|350px|Figure 1: On the left is shown a stack of images &lt;br /&gt;
and a sample pixel stack around a cortical region. On the left is shown the Gaussian(blue) fittet to &lt;br /&gt;
a real sample from the dataset we used along with the non-parametric density estimate(red). &lt;br /&gt;
Note that the distribution is bi-modal because of white matter-gray matter transaction.]]&lt;br /&gt;
&lt;br /&gt;
In order to align all subjects in the population,&lt;br /&gt;
we consider sum of pixelwise entropies as a joint alignment criterion.&lt;br /&gt;
The justification for this approach is that if the images are aligned properly, &lt;br /&gt;
intensity values at corresponding coordinate locations from all the images &lt;br /&gt;
will form a low entropy distribution.&lt;br /&gt;
This approach does not require the use of a reference subject; all&lt;br /&gt;
subjects are simultenously driven to the common tendency of the population.&lt;br /&gt;
&lt;br /&gt;
We employ a kernel based density estimation scheme to estimate univariate entropies.&lt;br /&gt;
Using the entropy measure we obtain a better treatment of transitions between different&lt;br /&gt;
tissue types, such as gray matter-white matter transitions in the cortical regions&lt;br /&gt;
where intensity distributions can be bi-modal as shown in Figure 1.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''Deformation Model''&lt;br /&gt;
&lt;br /&gt;
[[Image:GroupwiseBspline.png|thumb|350px|Figure 2: An example deformation field. The local neighborhood affecting the deformation is overlayed on the image.]]&lt;br /&gt;
&lt;br /&gt;
For the nonrigid deformation model,&lt;br /&gt;
we define a combined transformation consisting of &lt;br /&gt;
a global and a local component&lt;br /&gt;
&lt;br /&gt;
:&amp;lt;math&amp;gt;&lt;br /&gt;
T(\mathbf{x}) = T_{local}({T_{global}(\mathbf{x})})&lt;br /&gt;
&amp;lt;/math&amp;gt;&lt;br /&gt;
&lt;br /&gt;
where &amp;lt;math&amp;gt;T_{global}&amp;lt;/math&amp;gt; is a twelve parameter affine transform and &lt;br /&gt;
&amp;lt;math&amp;gt;T_{local}&amp;lt;/math&amp;gt; is a deformation model based on B-splines.&lt;br /&gt;
&lt;br /&gt;
The free form deformation can be written as the 3-D tensor product&lt;br /&gt;
of 1-D cubic B-splines.&lt;br /&gt;
&lt;br /&gt;
:&amp;lt;math&amp;gt;&lt;br /&gt;
T_{local}(\mathbf{x}) = \mathbf{x} + \sum_{l=0}^3\sum_{m=0}^3\sum_{n=0}^3 B_l(u)B_m(v)B_n(w) \Phi_{i+l,j+m,k+n}&lt;br /&gt;
&amp;lt;/math&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
		&lt;br /&gt;
where &amp;lt;math&amp;gt;B_l&amp;lt;/math&amp;gt; is &amp;lt;math&amp;gt;l&amp;lt;/math&amp;gt;'th cubic B-spline basis function. &amp;lt;math&amp;gt;(u,v,w)&amp;lt;/math&amp;gt; is the distance &lt;br /&gt;
to &amp;lt;math&amp;gt;(x,y,z)&amp;lt;/math&amp;gt; from the control point &amp;lt;math&amp;gt;\Phi_{i,j,k}&amp;lt;/math&amp;gt; as shown in Figure 2.&lt;br /&gt;
&lt;br /&gt;
The deformation of a given point can be found using only the control points in the neighborhood of the given point. Therefore,&lt;br /&gt;
optimization of the objective function can be implemented efficiently.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''Implementation''&lt;br /&gt;
&lt;br /&gt;
[[Image:GroupwiseIncreasingScale.PNG|thumb|350px|Figure 3: A registration schedule using gradually increasing deformation field complexity. From left to right deformation fields for increasing deformation field complexity. ]]&lt;br /&gt;
&lt;br /&gt;
We provide an efficient optimization scheme by using line search with the gradient descent algorithm.&lt;br /&gt;
For computational efficiency, we employ a stochastic subsampling procedure. &lt;br /&gt;
In each iteration of the algorithm, &lt;br /&gt;
a random subset is drawn from all samples and the objective function is evaluated&lt;br /&gt;
only on this sample set. &lt;br /&gt;
&lt;br /&gt;
To obtain a dense deformation field capturing anatomical variations at different scales,&lt;br /&gt;
we gradually increase the complexity of the deformation field by refining the grid of B-spline control points.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Image:GroupwiseMultiResolution.PNG|thumb|350px|Figure 4: An example showing the multi-resolution scheme. The registration is first performed at a coarse scale by downsampling the input.&lt;br /&gt;
Results from coarser scales are used to initialize&lt;br /&gt;
optimization at finer scales. Also note that the objective function is only evaluated on a small subset of input points. ]]&lt;br /&gt;
&lt;br /&gt;
As in every iterative search algorithm, local minima pose a significant problem. &lt;br /&gt;
To avoid local minima we use a multi-resolution optimization scheme for each resolution level of the deformation field.&lt;br /&gt;
&lt;br /&gt;
We implemented our groupwise registration method in a multi-threaded fashion using Insight Toolkit(ITK)&lt;br /&gt;
and made the implementation publicly available [http://www.na-mic.org/svn/NAMICSandBox/trunk/MultiImageRegistration/ (code)].&lt;br /&gt;
&lt;br /&gt;
''Results''&lt;br /&gt;
&lt;br /&gt;
[[Image:GroupwiseMeanImages.png|thumb|350px|Figure 5:  Central slices of 3D volumes for groupwise registration. Rows show mean and standard deviation images followed by label overlap images for GM, WM and CSF labels. Columns display the results for affine and B-splines with grid spacing 32, 16 and 8 voxels, respectively. ]]&lt;br /&gt;
[[Image:GroupwiseBarsWMGM.png|thumb|350px|Figure 6: GM, WM DICE measures computed for different deformation field resolution levels. Blue bars show the results for groupwise registration and the red bars show the results for registration to the mean setting.]]&lt;br /&gt;
[[Image:GroupwiseBarsManual.png|thumb|350px|Figure 7: DICE measures for manually segmented labels. Bars correspond to the same setting as in figure 6. ]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
We tested the groupwise registration algorithm on a MR brain dataset. &lt;br /&gt;
The dataset consists of 50 MR brain images of three subgroups:&lt;br /&gt;
schizophrenics, affected disorder and normal control patients. &lt;br /&gt;
MR images are T1 scans with 256x256x128 voxels &lt;br /&gt;
and 0.9375x0.9375x1.5 mm&amp;lt;sup&amp;gt;3&amp;lt;/sup&amp;gt; spacing. &lt;br /&gt;
For each image in the dataset, an automatic tissue classification&lt;br /&gt;
was performed, yielding gray matter (GM), white matter (WM) and cerebro-spinal&lt;br /&gt;
fluid (CSF) labels. In addition, manual segmentations of four subcortical regions &lt;br /&gt;
(left and right hippocampus and amygdala) and four cortical regions (left and right superior temporal &lt;br /&gt;
gyrus and para-hippocampus) were available for each MR image.&lt;br /&gt;
&lt;br /&gt;
Increasing the complexity of the deformation model improves the&lt;br /&gt;
accuracy of prediction. An interesting open problem is automatically&lt;br /&gt;
identifying the appropriate deformation complexity before the&lt;br /&gt;
registration overfits and the accuracy of prediction goes down.  We&lt;br /&gt;
also note that the alignment of the subcortical structures is much&lt;br /&gt;
better than that of the cortical regions. It is not surprising as the&lt;br /&gt;
registration algorithm does not use the information about geometry of the cortex&lt;br /&gt;
to optimize the alignment of the cortex. In addition, it has&lt;br /&gt;
been often observed that the cortical structures exhibit higher&lt;br /&gt;
variability across subjects when considered in the 3D volume rather&lt;br /&gt;
than modelled on the surface.&lt;br /&gt;
&lt;br /&gt;
Our experiments highlight the need for further research in developing&lt;br /&gt;
evaluation criteria for image alignment. We used the standard Dice&lt;br /&gt;
measure, but it is not clear that this measurement captures all the&lt;br /&gt;
nuances of the resulting alignment.&lt;br /&gt;
&lt;br /&gt;
Comparing the groupwise registration to the pairwise approach, we&lt;br /&gt;
observe that the sharpness of the mean images and the tissue overlaps&lt;br /&gt;
in Figure 5 look visually similar. From Figures 6 and 7, we note that&lt;br /&gt;
groupwise registration performs slightly better than the pairwise&lt;br /&gt;
setting in most of the cases, especially as we increase the complexity&lt;br /&gt;
of the warp. This suggests that considering the population as a whole&lt;br /&gt;
and registering subjects jointly brings the population into better&lt;br /&gt;
alignment than matching each subject to a mean template&lt;br /&gt;
image. However, the advantage shown here is only slight; more&lt;br /&gt;
comparative studies are needed of the two approaches.&lt;br /&gt;
&lt;br /&gt;
We compare our groupwise algorithm to a pairwise method where we register&lt;br /&gt;
each subject to the mean intensity using sum of square differences.&lt;br /&gt;
During each iteration we consider the mean image as a reference image&lt;br /&gt;
and register&lt;br /&gt;
every subject to the mean image using sum of squared differences. &lt;br /&gt;
After each iteration the mean image is updated and pairwise registrations are performed until convergence.&lt;br /&gt;
&lt;br /&gt;
The images in Figure 5 show central slices of 3D images after registration. &lt;br /&gt;
Visually, mean images get sharper and variance images becomes darker, especially around central ventricles and cortical regions. &lt;br /&gt;
We can observe that anatomical variability at cortical regions causes significant blur for &lt;br /&gt;
GM, WM and CSF structures using affine registration. &lt;br /&gt;
Finer scales of B-spline deformation fields capture a significant part of this anatomical variability and &lt;br /&gt;
the tissue label overlap images get sharper.&lt;br /&gt;
&lt;br /&gt;
=Asymmetric Image-Template Registration=&lt;br /&gt;
&lt;br /&gt;
A natural requirement in pairwise image registration is that the resulting deformation is independent of the order of the images. This constraint is typically achieved via a symmetric cost function and has been shown to reduce the eﬀects of local optima. Consequently, symmetric registration has been successfully applied to pairwise image registration as well as the spatial alignment of individual images with a template. However, recent work has shown that the relationship between &lt;br /&gt;
an image and a template is fundamentally asymmetric. In this paper, we develop a method that reconciles the practical advantages of symmetric registration with the asymmetric nature of image-template registration by adding a simple correction factor to the symmetric cost function. We instantiate our model within a log-domain diffeomorphic registration &lt;br /&gt;
framework. Our experiments show exploiting the asymmetry in image-template registration improves alignment in the image coordinates. &lt;br /&gt;
&lt;br /&gt;
= Key Investigators =&lt;br /&gt;
&lt;br /&gt;
* MIT: M.R. Sabuncu, B.T.T. Yeo, K. Van Leemput, S.K. Balci, P. Golland, S. Wells.&lt;br /&gt;
* Harvard DBP: S. Bouix, M.E. Shenton, B. Fischl.&lt;br /&gt;
&lt;br /&gt;
= Publications =&lt;br /&gt;
''In Print''&lt;br /&gt;
&lt;br /&gt;
* [http://www.na-mic.org/publications/pages/display?search=Projects%3AGroupwiseRegistration&amp;amp;submit=Search&amp;amp;words=all&amp;amp;title=checked&amp;amp;keywords=checked&amp;amp;authors=checked&amp;amp;abstract=checked&amp;amp;sponsors=checked&amp;amp;searchbytag=checked| NA-MIC Publications Database]&lt;br /&gt;
&lt;br /&gt;
[[Category: Registration]] [[Category:Segmentation]] [[Category:MRI]] [[Category:Schizophrenia]]&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Algorithm:MIT&amp;diff=42535</id>
		<title>Algorithm:MIT</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Algorithm:MIT&amp;diff=42535"/>
		<updated>2009-09-10T19:37:24Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: /* Groupwise Registration */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; Back to [[Algorithm:Main|NA-MIC Algorithms]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
= Overview of MIT Algorithms (PI: Polina Golland) =&lt;br /&gt;
&lt;br /&gt;
Our group seeks to model statistical variability of anatomy and function across subjects and between populations and to utilize computational models of such variability to improve predictions for individual subjects, as well as characterize populations. Our long-term goal is to develop methods for joint modeling of anatomy and function and to apply them in clinical and scientific studies. We work primarily with anatomical, DTI and fMRI images. We actively contribute implementations of our algorithms to the NAMIC-kit.&lt;br /&gt;
&lt;br /&gt;
= MIT Projects =&lt;br /&gt;
&lt;br /&gt;
{| cellpadding=&amp;quot;10&amp;quot; style=&amp;quot;text-align:left;&amp;quot;&lt;br /&gt;
|| [[Image:Segmentation_example2.png|250px]]&lt;br /&gt;
||&lt;br /&gt;
&lt;br /&gt;
== [[Projects:NonparametricSegmentation| Nonparametric Models for Supervised Image Segmentation]] ==&lt;br /&gt;
&lt;br /&gt;
We propose a non-parametric, probabilistic model for the automatic segmentation of medical images,&lt;br /&gt;
given a training set of images and corresponding label maps. The resulting inference algorithms we&lt;br /&gt;
develop rely on pairwise registrations between the test image and individual training images. The&lt;br /&gt;
training labels are then transferred to the test image and fused to compute a final segmentation of&lt;br /&gt;
the test subject. [[Projects:NonparametricSegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; Supervised Nonparametric Image Parcellation, M.R. Sabuncu, B.T. Thomas Yeo, K. Van Leemput, B. Fischl, and P. Golland. To appear in Proceedings of the International Conference on Medical Image Computing and Computer Assisted Intervention (MICCAI), 2009.&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; Nonparametric Mixture Models for Supervised Image Parcellation, M.R. Sabuncu, &lt;br /&gt;
B.T.T. Yeo, K. Van Leemput, B. Fischl, and P. Golland. To be presented at PMMIA Workshop at MICCAI 2009.   &lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{| cellpadding=&amp;quot;10&amp;quot; style=&amp;quot;text-align:left;&amp;quot;&lt;br /&gt;
| style=&amp;quot;width:15%&amp;quot; | [[Image:MITHippocampalSubfieldSegmentation.png|250px]]&lt;br /&gt;
| style=&amp;quot;width:85%&amp;quot; |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:BayesianMRSegmentation| Bayesian Segmentation of MRI Images]] ==&lt;br /&gt;
&lt;br /&gt;
The aim of this project is to develop, implement, and validate a generic method for automatically segmenting MRI images that automatically adapts to different acquisition sequences. [[Projects:BayesianMRSegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; Automated Segmentation of Hippocampal Subﬁelds from Ultra-High Resolution In Vivo MRI, K. Van Leemput, A. Bakkour, T. Benner, G. Wiggins, L.L. Wald, J. Augustinack, B.C. Dickerson, P. Golland, and B. Fischl. Hippocampus, vol. 19, no. 6, pp. 549-557, June 2009&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; Encoding Probabilistic Atlases Using Bayesian Inference, K. Van Leemput. IEEE Transactions on Medical Imaging, vol. 28, no. 6, pp. 822-837, June 2009&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:ICluster_templates.gif|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:MultimodalAtlas|Multimodal Atlas]] ==&lt;br /&gt;
&lt;br /&gt;
In this work, we propose and investigate an algorithm that jointly co-registers a collection of images while computing multiple templates. The algorithm, called '''iCluster''', is used to compute multiple atlases for a given population.&lt;br /&gt;
[[Projects:MultimodalAtlas|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; Image-driven Population Analysis through Mixture-Modeling, M.R. Sabuncu, S.K. Balci, M.E. Shenton and P. Golland. IEEE Transactions on Medical Imaging. Accepted for Publication, 2009.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:CoordinateChart.png|250px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:SphericalDemons|Spherical Demons: Fast Surface Registration]] ==&lt;br /&gt;
&lt;br /&gt;
We present the fast Spherical Demons algorithm for registering two spherical images. By exploiting spherical vector spline interpolation theory, we show that a large class of regularizers for the modified demons objective function can be efficiently approximated on the sphere using convolution. Based on the one parameter subgroups of diffeomorphisms, [[Projects:SphericalDemons|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; B.T.T. Yeo, M. Sabuncu, T. Vercauteren, N. Ayache, B. Fischl, P. Golland. Spherical Demons: Fast Surface Registration. MICCAI, volume 5241 of LNCS, 745--753, 2008.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:JointRegSeg.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:RegistrationRegularization|Optimal Atlas Regularization in Image Segmentation]] ==&lt;br /&gt;
&lt;br /&gt;
We propose a unified framework for computing atlases from manually labeled data sets at various degrees of “sharpness” and the joint registration and segmentation of a new brain with these atlases. Using this framework, we investigate the tradeoff between warp regularization and image ﬁdelity, i.e. the smoothness of the new subject warp and the sharpness of the atlas in a segmentation application.&lt;br /&gt;
[[Projects:RegistrationRegularization|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; B.T.T. Yeo, M.R. Sabuncu, R. Desikan, B. Fischl, P. Golland. Effects of Registration Regularization and Atlas Sharpness on Segmentation Accuracy. Medical Image Analysis, 12(5):603--615, 2008. &lt;br /&gt;
  &lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:epi_correction_small.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:FieldmapFreeDistortionCorrection|Fieldmap-Free EPI Distortion Correction]] ==&lt;br /&gt;
&lt;br /&gt;
In this project we aim to improve the EPI distortion correction algorithms [[Projects:FieldmapFreeDistortionCorrection|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt;  Poynton C., Jenkinson M., Whalen S., Golby A.J., Wells III W. Fieldmap-Free Retrospective Registration and Distortion Correction for EPI-Based Functiona Imaging. MICCAI 2008.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:mit_fmri_clustering_parcellation2_xsub.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:fMRIClustering|fMRI clustering]] ==&lt;br /&gt;
&lt;br /&gt;
In this project we study the application of model-based clustering algorithms in identification of functional connectivity in the brain. [[Projects:fMRIClustering|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; A. Venkataraman, K.R.A. Van Dijk, R.L. Buckner, P. Golland. Exploring Functional Connectivity in fMRI via Clustering. ICASSP 2009. &lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; D. Lashkari, E. Vul, N. Kanwisher, P. Golland. Discovering Structure in the Space of Activation&lt;br /&gt;
Profiles in fMRI. MICCAI 2008. &lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:FoldingSpeedDetection.png|150px|]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeAnalysisWithOvercompleteWavelets|Shape Analysis With Overcomplete Wavelets]] ==&lt;br /&gt;
&lt;br /&gt;
In this work, we extend the Euclidean wavelets to the sphere. The resulting over-complete spherical wavelets are invariant to the rotation of the spherical image parameterization. We apply the over-complete spherical wavelet to cortical folding development [[Projects:ShapeAnalysisWithOvercompleteWavelets|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; B.T.T. Yeo, P. Yu, P.E. Grant, B. Fischl, P. Golland. Shape Analysis with Overcomplete Spherical Wavelets. Proceedings of the International Conference on Medical Image Computing and Computer Assisted Intervention (MICCAI), volume 5241 of LNCS, 468--476, 2008&lt;br /&gt;
&lt;br /&gt;
B.T.T. Yeo, W. Ou, P. Golland. On the Construction of Invertible Filter Banks on the 2-Sphere. Yeo, Ou and Golland. IEEE Transactions on Image Processing. 17(3):283--300. 2008. &lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:Models.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIModeling|Fiber Tract Modeling, Clustering, and Quantitative Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this work is to model the shape of the fiber bundles and use this model description in clustering and statistical analysis of fiber tracts. [[Projects:DTIModeling|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; Mahnaz Maddah, Marek Kubicki, William M. Wells, Carl-Fredrik Westin, Martha E. Shenton and W. Eric L. Grimson, Findings in Schizophrenia by Tract-Oriented DT-MRI Analysis. MICCAI 2008.&lt;br /&gt;
&lt;br /&gt;
M. Maddah, L. Zollei, W. E. L. Grimson, W. M. Wells, Modeling of Anatomical Information in Clustering of White Matter Fiber Trajectories Using Dirichlet Distribution. MMBIA 2008.&lt;br /&gt;
&lt;br /&gt;
M. Maddah, L. Zollei, W. E. L. Grimson, C-F Westin, W. M. Wells, A Mathematical Framework for Incorporating Anatomical Knowledge in DT-MRI Analysis. ISBI 2008.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:TGIt.gif| 150px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:LatentAtlasSegmentation|Joint Segmentation of Image Ensembles via Latent Atlases]] ==&lt;br /&gt;
&lt;br /&gt;
Spatial priors, such as probabilistic atlases, play an important role in MRI segmentation. The atlases are typically generated by averaging manual labels of aligned brain regions across different subjects. However, the availability of comprehensive, reliable and suitable manual segmentations is limited. We therefore propose a joint segmentation of corresponding, aligned structures in the entire population that does not require a probability atlas. &lt;br /&gt;
[[Projects:LatentAtlasSegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt;  T. Riklin Raviv, K. Van Leemput, W.M. Wells III and P. Golland, Joint Segmentation of Image Ensembles via Latent Atlases, Proceedings of the International Conference on Medical Image Computing and Computer Assisted Intervention (MICCAI), 2009&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; &lt;br /&gt;
T. Riklin Raviv, B.H. Menze, K. Van Leemput, B. Stieltjes,  M.A. Weber, N. Ayache, W. M. Wells III and P. Golland, Joint Segmentation using Patient specific Latent Anatomy Model&lt;br /&gt;
MICCAI workshop for Probabilistic Models on Medical Image Analysis (PMMIA) 2009 &lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:Progress_Registration_Segmentation_Shape.jpg|180px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeBasedSegmentationAndRegistration|Shape Based Segmentation and Registration]] ==&lt;br /&gt;
&lt;br /&gt;
This type of algorithm assigns a tissue type to each voxel in the volume. Incorporating prior shape information biases the label assignment towards contiguous regions that are consistent with the shape model. [[Projects:ShapeBasedSegmentationAndRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:GroupwiseSummary.PNG|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:GroupwiseRegistration|Groupwise Registration]] ==&lt;br /&gt;
&lt;br /&gt;
We extend a previously demonstrated entropy based groupwise registration method to include a free-form deformation model based on B-splines. We provide an efficient implementation using stochastic gradient descents in a multi-resolution setting. We demonstrate the method in application to a set of 50 MRI brain scans and compare the results to a pairwise approach using segmentation labels to evaluate the quality of alignment.&lt;br /&gt;
&lt;br /&gt;
In a related project,  we develop a method that reconciles the practical advantages of symmetric registration with the asymmetric nature of image-template registration by adding a simple correction factor to the symmetric cost function. We instantiate our model within a log-domain diffeomorphic registration framework. Our experiments show exploiting the asymmetry in image-template registration improves alignment in the image coordinates.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt;  Asymmetric Image-Template Registration, M.R. Sabuncu, B.T. Thomas Yeo, T. Vercauteren, K. Van Leemput, P. Golland. To appear in Proceedings of the International Conference on Medical Image Computing and Computer Assisted Intervention (MICCAI), 2009&lt;br /&gt;
&lt;br /&gt;
[[Projects:GroupwiseRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:MIT_DTI_JointSegReg_atlas3D.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIFiberRegistration|Joint Registration and Segmentation of DWI Fiber Tractography]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this work is to jointly register and cluster DWI fiber tracts obtained from a group of subjects. [[Projects:DTIFiberRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:brain.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIClustering|DTI Fiber Clustering and Fiber-Based Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this project is to provide structural description of the white matter architecture as a partition into coherent fiber bundles and clusters, and to use these bundles for quantitative measurement. [[Projects:DTIClustering|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:FMRIEvaluationchart.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:fMRIDetection|fMRI Detection and Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
We are exploring algorithms for improved fMRI detection and interpretation by incorporting spatial priors and anatomical information to guide the detection. [[Projects:fMRIDetection|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:Thalamus_algo_outline.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTISegmentation|DTI-based Segmentation]] ==&lt;br /&gt;
&lt;br /&gt;
Unlike conventional MRI, DTI provides adequate contrast to segment the thalamic nuclei, which are gray matter structures. [[Projects:DTISegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:ConnectivityMap.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIStochasticTractography|Stochastic Tractography]] ==&lt;br /&gt;
&lt;br /&gt;
This work calculates posterior distributions of white matter fiber tract parameters given diffusion observations in a DWI volume.  [[Projects:DTIStochasticTractography|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:HippocampalShapeDifferences.gif|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeAnalysis|Population Analysis of Anatomical Variability]] ==&lt;br /&gt;
&lt;br /&gt;
Our goal is to develop mathematical approaches to modeling anatomical variability within and across populations using tools like local shape descriptors of specific regions of interest and global constellation descriptors of multiple ROI's. [[Projects:ShapeAnalysis|More...]]&lt;br /&gt;
&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:NonparametricSegmentation&amp;diff=42526</id>
		<title>Projects:NonparametricSegmentation</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:NonparametricSegmentation&amp;diff=42526"/>
		<updated>2009-09-10T19:33:07Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;=Introduction=&lt;br /&gt;
&lt;br /&gt;
We propose a non-parametric, probabilistic model for the automatic segmentation of medical images, given a training set of images and corresponding label maps. The resulting inference algorithms we develop rely on pairwise registrations between the test image and individual training images. The training labels are then transferred to the test image and fused to compute a final segmentation of the test subject. Label fusion methods have been shown to yield accurate segmentation, since the use&lt;br /&gt;
of multiple registrations captures greater inter-subject anatomical variability and improves robustness against occasional registration failures, cf. [1,2,3]. To the best of our knowledge, this project investigates the first comprehensive probabilistic framework that rigorously motivates label fusion as a segmentation approach. The proposed framework allows us to compare different label fusion algorithms theoretically and practically. In particular, recent label fusion or multi-atlas segmentation algorithms are interpreted as special cases of our framework.&lt;br /&gt;
&lt;br /&gt;
=Application: Brain MRI=&lt;br /&gt;
We instantiate our model in the context of brain MRI segmentation, where whole brain MRI volumes are automatically parcellated into the following anatomical Regions of Interest (ROI): white matter (WM), cerebral cortex(CT), lateral ventricle (LV), hippocampus(HP), amygdala (AM), thalamus (TH), caudate (CA), putamen (PU), palladum (PA). &lt;br /&gt;
The proposed non-parametric model yields four types of label fusion algorithms: &lt;br /&gt;
&lt;br /&gt;
'''(1) Majority Voting:''' The algorithm computes the most frequent propagated labels at each voxel independently. This is a segmentation algorithm commonly used in practice, e.g. [2,3].&lt;br /&gt;
&lt;br /&gt;
'''(2) Local Label Fusion:''' An independent weighted averaging of propagated labels, where the weights vary at each voxel and are a function of the intensity difference between the training image and test image.&lt;br /&gt;
&lt;br /&gt;
'''(3) Semi-Local Label Fusion:''' Propagated labels are fused in a weighted fashion using a variational mean field algorithm. The weights are encouraged to be similar in local patches.&lt;br /&gt;
&lt;br /&gt;
'''(4) Global Label Fusion:''' Propagated labels are fused in a weighted fashion using an Expectation Maximization algorithm. The weights are global, i.e., there is a single weight for each training subject.&lt;br /&gt;
&lt;br /&gt;
The following figure shows an example segmentation obtained via Local Label Fusion.&lt;br /&gt;
&lt;br /&gt;
[[File:Segmentation_example2.png]]&lt;br /&gt;
&lt;br /&gt;
=Experiments=&lt;br /&gt;
We conduct two sets of experiments to validate our framework. In the first set of experiments, we use 39 brain MRI scans – with manually segmented white matter, cerebral cortex, ventricles and subcortical structures – to compare different label fusion algorithms and the widely-used Freesurfer whole-brain segmentation tool [4]. &lt;br /&gt;
&lt;br /&gt;
The following figure shows the Boxplots of Dice scores for all methods: Freesurfer (red), Majority Voting (yellow), Global Weighted Fusion (green), Local Weighted Voting (blue), Semi-local Weighted Fusion (purple).&lt;br /&gt;
&lt;br /&gt;
[[File:DiceScoresPerROI.png]]&lt;br /&gt;
&lt;br /&gt;
Our results indicate that the proposed framework yields more accurate segmentation than Freesurfer and Majority Voting. &lt;br /&gt;
&lt;br /&gt;
In a second experiment, we use brain MRI scans of 304 subjects to demonstrate that the proposed segmentation tool is sufficiently sensitive to robustly detect hippocampal atrophy that foreshadows the onset of Alzheimer’s Disease.&lt;br /&gt;
The following figure plots the Average Hippocampal volumes for five different groups (young: younger than 30, middle aged: older than 30, younger than 60; old: older than 60; patients with MCI, and AD patients) in the 304 subjects of Experiment 2. Error bars indicate standard error.&lt;br /&gt;
&lt;br /&gt;
[[File:HippocampalVolume.png]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=Conclusion=&lt;br /&gt;
In this work, we investigate a generative model that leads to label fusion style image segmentation methods. Within the proposed framework, we derived various algorithms that combine transferred training labels into a single segmentation estimate. With a dataset of 39 brain MRI scans and corresponding label maps obtained from an expert, we experimentally compared these segmentation algorithms with Freesurfer’s widely-used atlas-based segmentation tool [4]. Our results suggested that the proposed framework yields accurate and robust segmentation tools that can be employed on large multi-subject datasets. In a second experiment, we employed one of the developed segmentation algorithms to compute hippocampal volumes in MRI scans of 304 subjects. A comparison of these measurements across clinical and age groups indicate that the proposed algorithms are sufficiently sensitive to detect hippocampal atrophy that precedes probable onset of Alzheimer’s Disease.&lt;br /&gt;
&lt;br /&gt;
=Publications=&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; Supervised Nonparametric Image Parcellation, M.R. Sabuncu, B.T. Thomas Yeo, K. Van Leemput, B. Fischl, and P. Golland. To appear in Proceedings of the International Conference on Medical Image Computing and Computer Assisted Intervention (MICCAI), 2009.&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; Nonparametric Mixture Models for Supervised Image Parcellation, M.R. Sabuncu, &lt;br /&gt;
B.T.T. Yeo, K. Van Leemput, B. Fischl, and P. Golland. To be presented at PMMIA Workshop at MICCAI 2009. &lt;br /&gt;
&lt;br /&gt;
= Key Investigators =&lt;br /&gt;
&lt;br /&gt;
*MIT: Mert R. Sabuncu, B.T. Thomas Yeo, Koen Van Leemput and Polina Golland&lt;br /&gt;
&lt;br /&gt;
*Harvard: Koen Van Leemput and Bruce Fischl&lt;br /&gt;
&lt;br /&gt;
=Literature=&lt;br /&gt;
[1] X. Artaechevarria, A. Munoz-Barrutia, and C. Ortiz de Solorzano. Combination strategies in multi-atlas image segmentation:&lt;br /&gt;
Application to brain MR data. IEEE Tran. Med. Imaging, 28(8):1266 – 1277, 2009.&lt;br /&gt;
&lt;br /&gt;
[2] R.A. Heckemann, J.V. Hajnal, P. Aljabar, D. Rueckert, and A. Hammers. Automatic anatomical brain MRI segmentation&lt;br /&gt;
combining label propagation and decision fusion. Neuroimage, 33(1):115–126, 2006.&lt;br /&gt;
&lt;br /&gt;
[3] T. Rohlfing, R. Brandt, R. Menzel, and C.R. Maurer. Evaluation of atlas selection strategies for atlas-based image&lt;br /&gt;
segmentation with application to confocal microscopy images of bee brains. NeuroImage, 21(4):1428–1442, 2004.&lt;br /&gt;
&lt;br /&gt;
[4] Freesurfer Wiki. http://surfer.nmr.mgh.harvard.edu.&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:NonparametricSegmentation&amp;diff=42525</id>
		<title>Projects:NonparametricSegmentation</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:NonparametricSegmentation&amp;diff=42525"/>
		<updated>2009-09-10T19:31:30Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;=Introduction=&lt;br /&gt;
&lt;br /&gt;
We propose a non-parametric, probabilistic model for the automatic segmentation of medical images, given a training set of images and corresponding label maps. The resulting inference algorithms we develop rely on pairwise registrations between the test image and individual training images. The training labels are then transferred to the test image and fused to compute a final segmentation of the test subject. Label fusion methods have been shown to yield accurate segmentation, since the use&lt;br /&gt;
of multiple registrations captures greater inter-subject anatomical variability and improves robustness against occasional registration failures, cf. [1,2,3]. To the best of our knowledge, this project investigates the first comprehensive probabilistic framework that rigorously motivates label fusion as a segmentation approach. The proposed framework allows us to compare different label fusion algorithms theoretically and practically. In particular, recent label fusion or multi-atlas segmentation algorithms are interpreted as special cases of our framework.&lt;br /&gt;
&lt;br /&gt;
=Application: Brain MRI=&lt;br /&gt;
We instantiate our model in the context of brain MRI segmentation, where whole brain MRI volumes are automatically parcellated into the following anatomical Regions of Interest (ROI): white matter (WM), cerebral cortex(CT), lateral ventricle (LV), hippocampus(HP), amygdala (AM), thalamus (TH), caudate (CA), putamen (PU), palladum (PA). &lt;br /&gt;
The proposed non-parametric model yields four types of label fusion algorithms: &lt;br /&gt;
&lt;br /&gt;
'''(1) Majority Voting:''' The algorithm computes the most frequent propagated labels at each voxel independently. This is a segmentation algorithm commonly used in practice, e.g. [2,3].&lt;br /&gt;
&lt;br /&gt;
'''(2) Local Label Fusion:''' An independent weighted averaging of propagated labels, where the weights vary at each voxel and are a function of the intensity difference between the training image and test image.&lt;br /&gt;
&lt;br /&gt;
'''(3) Semi-Local Label Fusion:''' Propagated labels are fused in a weighted fashion using a variational mean field algorithm. The weights are encouraged to be similar in local patches.&lt;br /&gt;
&lt;br /&gt;
'''(4) Global Label Fusion:''' Propagated labels are fused in a weighted fashion using an Expectation Maximization algorithm. The weights are global, i.e., there is a single weight for each training subject.&lt;br /&gt;
&lt;br /&gt;
The following figure shows an example segmentation obtained via Local Label Fusion.&lt;br /&gt;
&lt;br /&gt;
[[File:Segmentation_example2.png]]&lt;br /&gt;
&lt;br /&gt;
=Experiments=&lt;br /&gt;
We conduct two sets of experiments to validate our framework. In the first set of experiments, we use 39 brain MRI scans – with manually segmented white matter, cerebral cortex, ventricles and subcortical structures – to compare different label fusion algorithms and the widely-used Freesurfer whole-brain segmentation tool [4]. &lt;br /&gt;
&lt;br /&gt;
The following figure shows the Boxplots of Dice scores for all methods: Freesurfer (red), Majority Voting (yellow), Global Weighted Fusion (green), Local Weighted Voting (blue), Semi-local Weighted Fusion (purple).&lt;br /&gt;
&lt;br /&gt;
[[File:DiceScoresPerROI.png]]&lt;br /&gt;
&lt;br /&gt;
Our results indicate that the proposed framework yields more accurate segmentation than Freesurfer and Majority Voting. &lt;br /&gt;
&lt;br /&gt;
In a second experiment, we use brain MRI scans of 304 subjects to demonstrate that the proposed segmentation tool is sufficiently sensitive to robustly detect hippocampal atrophy that foreshadows the onset of Alzheimer’s Disease.&lt;br /&gt;
The following figure plots the Average Hippocampal volumes for five different groups (young: younger than 30, middle aged: older than 30, younger than 60; old: older than 60; patients with MCI, and AD patients) in the 304 subjects of Experiment 2. Error bars indicate standard error.&lt;br /&gt;
&lt;br /&gt;
[[File:HippocampalVolume.png]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=Conclusion=&lt;br /&gt;
In this work, we investigate a generative model that leads to label fusion style image segmentation methods. Within the proposed framework, we derived various algorithms that combine transferred training labels into a single segmentation estimate. With a dataset of 39 brain MRI scans and corresponding label maps obtained from an expert, we experimentally compared these segmentation algorithms with Freesurfer’s widely-used atlas-based segmentation tool [4]. Our results suggested that the proposed framework yields accurate and robust segmentation tools that can be employed on large multi-subject datasets. In a second experiment, we employed one of the developed segmentation algorithms to compute hippocampal volumes in MRI scans of 304 subjects. A comparison of these measurements across clinical and age groups indicate that the proposed algorithms are sufficiently sensitive to detect hippocampal atrophy that precedes probable onset of Alzheimer’s Disease.&lt;br /&gt;
&lt;br /&gt;
=Publications=&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; Supervised Nonparametric Image Parcellation, M.R. Sabuncu, B.T. Thomas Yeo, K. Van Leemput, B. Fischl, and P. Golland. To appear in Proceedings of the International Conference on Medical Image Computing and Computer Assisted Intervention (MICCAI), 2009.&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; Nonparametric Mixture Models for Supervised Image Parcellation, M.R. Sabuncu, &lt;br /&gt;
B.T.T. Yeo, K. Van Leemput, B. Fischl, and P. Golland. To be presented at PMMIA Workshop at MICCAI 2009. &lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=Literature=&lt;br /&gt;
[1] X. Artaechevarria, A. Munoz-Barrutia, and C. Ortiz de Solorzano. Combination strategies in multi-atlas image segmentation:&lt;br /&gt;
Application to brain MR data. IEEE Tran. Med. Imaging, 28(8):1266 – 1277, 2009.&lt;br /&gt;
&lt;br /&gt;
[2] R.A. Heckemann, J.V. Hajnal, P. Aljabar, D. Rueckert, and A. Hammers. Automatic anatomical brain MRI segmentation&lt;br /&gt;
combining label propagation and decision fusion. Neuroimage, 33(1):115–126, 2006.&lt;br /&gt;
&lt;br /&gt;
[3] T. Rohlfing, R. Brandt, R. Menzel, and C.R. Maurer. Evaluation of atlas selection strategies for atlas-based image&lt;br /&gt;
segmentation with application to confocal microscopy images of bee brains. NeuroImage, 21(4):1428–1442, 2004.&lt;br /&gt;
&lt;br /&gt;
[4] Freesurfer Wiki. http://surfer.nmr.mgh.harvard.edu.&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:NonparametricSegmentation&amp;diff=42524</id>
		<title>Projects:NonparametricSegmentation</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:NonparametricSegmentation&amp;diff=42524"/>
		<updated>2009-09-10T19:30:57Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;=Introduction=&lt;br /&gt;
&lt;br /&gt;
We propose a non-parametric, probabilistic model for the automatic segmentation of medical images, given a training set of images and corresponding label maps. The resulting inference algorithms we develop rely on pairwise registrations between the test image and individual training images. The training labels are then transferred to the test image and fused to compute a final segmentation of the test subject. Label fusion methods have been shown to yield accurate segmentation, since the use&lt;br /&gt;
of multiple registrations captures greater inter-subject anatomical variability and improves robustness against occasional registration failures, cf. [1,2,3]. To the best of our knowledge, this project investigates the first comprehensive probabilistic framework that rigorously motivates label fusion as a segmentation approach. The proposed framework allows us to compare different label fusion algorithms theoretically and practically. In particular, recent label fusion or multi-atlas segmentation algorithms are interpreted as special cases of our framework.&lt;br /&gt;
&lt;br /&gt;
=Application: Brain MRI=&lt;br /&gt;
We instantiate our model in the context of brain MRI segmentation, where whole brain MRI volumes are automatically parcellated into the following anatomical Regions of Interest (ROI): white matter (WM), cerebral cortex(CT), lateral ventricle (LV), hippocampus(HP), amygdala (AM), thalamus (TH), caudate (CA), putamen (PU), palladum (PA). &lt;br /&gt;
The proposed non-parametric model yields four types of label fusion algorithms: &lt;br /&gt;
&lt;br /&gt;
'''(1) Majority Voting:''' The algorithm computes the most frequent propagated labels at each voxel independently. This is a segmentation algorithm commonly used in practice, e.g. [2,3].&lt;br /&gt;
&lt;br /&gt;
'''(2) Local Label Fusion:''' An independent weighted averaging of propagated labels, where the weights vary at each voxel and are a function of the intensity difference between the training image and test image.&lt;br /&gt;
&lt;br /&gt;
'''(3) Semi-Local Label Fusion:''' Propagated labels are fused in a weighted fashion using a variational mean field algorithm. The weights are encouraged to be similar in local patches.&lt;br /&gt;
&lt;br /&gt;
'''(4) Global Label Fusion:''' Propagated labels are fused in a weighted fashion using an Expectation Maximization algorithm. The weights are global, i.e., there is a single weight for each training subject.&lt;br /&gt;
&lt;br /&gt;
The following figure shows an example segmentation obtained via Local Label Fusion.&lt;br /&gt;
&lt;br /&gt;
[[File:Segmentation_example2.png]]&lt;br /&gt;
&lt;br /&gt;
=Experiments=&lt;br /&gt;
We conduct two sets of experiments to validate our framework. In the first set of experiments, we use 39 brain MRI scans – with manually segmented white matter, cerebral cortex, ventricles and subcortical structures – to compare different label fusion algorithms and the widely-used Freesurfer whole-brain segmentation tool [4]. &lt;br /&gt;
&lt;br /&gt;
The following figure shows the Boxplots of Dice scores for all methods: Freesurfer (red), Majority Voting (yellow), Global Weighted Fusion (green), Local Weighted Voting (blue), Semi-local Weighted Fusion (purple).&lt;br /&gt;
&lt;br /&gt;
[[File:DiceScoresPerROI.png]]&lt;br /&gt;
&lt;br /&gt;
Our results indicate that the proposed framework yields more accurate segmentation than Freesurfer and Majority Voting. &lt;br /&gt;
&lt;br /&gt;
In a second experiment, we use brain MRI scans of 304 subjects to demonstrate that the proposed segmentation tool is sufficiently sensitive to robustly detect hippocampal atrophy that foreshadows the onset of Alzheimer’s Disease.&lt;br /&gt;
The following figure plots the Average Hippocampal volumes for five different groups (young: younger than 30, middle aged: older than 30, younger than 60; old: older than 60; patients with MCI, and AD patients) in the 304 subjects of Experiment 2. Error bars indicate standard error.&lt;br /&gt;
&lt;br /&gt;
[[File:HippocampalVolume.png]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=Conclusion=&lt;br /&gt;
In this work, we investigate a generative model that leads to label fusion style image segmentation methods. Within the proposed framework, we derived various algorithms that combine transferred training labels into a single segmentation estimate. With a dataset of 39 brain MRI scans and corresponding label maps obtained from an expert, we experimentally compared these segmentation algorithms with Freesurfer’s widely-used atlas-based segmentation tool [4]. Our results suggested that the proposed framework yields accurate and robust segmentation tools that can be employed on large multi-subject datasets. In a second experiment, we employed one of the developed segmentation algorithms to compute hippocampal volumes in MRI scans of 304 subjects. A comparison of these measurements across clinical and age groups indicate that the proposed algorithms are sufficiently sensitive to detect hippocampal atrophy that precedes probable onset of Alzheimer’s Disease.&lt;br /&gt;
&lt;br /&gt;
=Publications=&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=Literature=&lt;br /&gt;
[1] X. Artaechevarria, A. Munoz-Barrutia, and C. Ortiz de Solorzano. Combination strategies in multi-atlas image segmentation:&lt;br /&gt;
Application to brain MR data. IEEE Tran. Med. Imaging, 28(8):1266 – 1277, 2009.&lt;br /&gt;
&lt;br /&gt;
[2] R.A. Heckemann, J.V. Hajnal, P. Aljabar, D. Rueckert, and A. Hammers. Automatic anatomical brain MRI segmentation&lt;br /&gt;
combining label propagation and decision fusion. Neuroimage, 33(1):115–126, 2006.&lt;br /&gt;
&lt;br /&gt;
[3] T. Rohlfing, R. Brandt, R. Menzel, and C.R. Maurer. Evaluation of atlas selection strategies for atlas-based image&lt;br /&gt;
segmentation with application to confocal microscopy images of bee brains. NeuroImage, 21(4):1428–1442, 2004.&lt;br /&gt;
&lt;br /&gt;
[4] Freesurfer Wiki. http://surfer.nmr.mgh.harvard.edu.&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:NonparametricSegmentation&amp;diff=42520</id>
		<title>Projects:NonparametricSegmentation</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:NonparametricSegmentation&amp;diff=42520"/>
		<updated>2009-09-10T19:29:11Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;=Introduction=&lt;br /&gt;
&lt;br /&gt;
We propose a non-parametric, probabilistic model for the automatic segmentation of medical images, given a training set of images and corresponding label maps. The resulting inference algorithms we develop rely on pairwise registrations between the test image and individual training images. The training labels are then transferred to the test image and fused to compute a final segmentation of the test subject. Label fusion methods have been shown to yield accurate segmentation, since the use&lt;br /&gt;
of multiple registrations captures greater inter-subject anatomical variability and improves robustness against occasional registration failures, cf. [1,2,3]. To the best of our knowledge, this project investigates the first comprehensive probabilistic framework that rigorously motivates label fusion as a segmentation approach. The proposed framework allows us to compare different label fusion algorithms theoretically and practically. In particular, recent label fusion or multi-atlas segmentation algorithms are interpreted as special cases of our framework.&lt;br /&gt;
&lt;br /&gt;
=Application: Brain MRI=&lt;br /&gt;
We instantiate our model in the context of brain MRI segmentation, where whole brain MRI volumes are automatically parcellated into the following anatomical Regions of Interest (ROI): white matter (WM), cerebral cortex(CT), lateral ventricle (LV), hippocampus(HP), amygdala (AM), thalamus (TH), caudate (CA), putamen (PU), palladum (PA). &lt;br /&gt;
The proposed non-parametric model yields four types of label fusion algorithms: &lt;br /&gt;
&lt;br /&gt;
'''(1) Majority Voting:''' The algorithm computes the most frequent propagated labels at each voxel independently. This is a segmentation algorithm commonly used in practice, e.g. [2,3].&lt;br /&gt;
&lt;br /&gt;
'''(2) Local Label Fusion:''' An independent weighted averaging of propagated labels, where the weights vary at each voxel and are a function of the intensity difference between the training image and test image.&lt;br /&gt;
&lt;br /&gt;
'''(3) Semi-Local Label Fusion:''' Propagated labels are fused in a weighted fashion using a variational mean field algorithm. The weights are encouraged to be similar in local patches.&lt;br /&gt;
&lt;br /&gt;
'''(4) Global Label Fusion:''' Propagated labels are fused in a weighted fashion using an Expectation Maximization algorithm. The weights are global, i.e., there is a single weight for each training subject.&lt;br /&gt;
&lt;br /&gt;
The following figure shows an example segmentation obtained via Local Label Fusion.&lt;br /&gt;
&lt;br /&gt;
[[File:Segmentation_example2.png]]&lt;br /&gt;
&lt;br /&gt;
=Experiments=&lt;br /&gt;
We conduct two sets of experiments to validate our framework. In the first set of experiments, we use 39 brain MRI scans – with manually segmented white matter, cerebral cortex, ventricles and subcortical structures – to compare different label fusion algorithms and the widely-used Freesurfer whole-brain segmentation tool [4]. &lt;br /&gt;
&lt;br /&gt;
The following figure shows the Boxplots of Dice scores for all methods: Freesurfer (red), Majority Voting (yellow), Global Weighted Fusion (green), Local Weighted Voting (blue), Semi-local Weighted Fusion (purple).&lt;br /&gt;
&lt;br /&gt;
[[File:DiceScoresPerROI.png]]&lt;br /&gt;
&lt;br /&gt;
Our results indicate that the proposed framework yields more accurate segmentation than Freesurfer and Majority Voting. &lt;br /&gt;
&lt;br /&gt;
In a second experiment, we use brain MRI scans of 304 subjects to demonstrate that the proposed segmentation tool is sufficiently sensitive to robustly detect hippocampal atrophy that foreshadows the onset of Alzheimer’s Disease.&lt;br /&gt;
The following figure plots the Average Hippocampal volumes for five different groups (young: younger than 30, middle aged: older than 30, younger than 60; old: older than 60; patients with MCI, and AD patients) in the 304 subjects of Experiment 2. Error bars indicate standard error.&lt;br /&gt;
&lt;br /&gt;
[[File:HippocampalVolume.png]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=Literature=&lt;br /&gt;
[1] X. Artaechevarria, A. Munoz-Barrutia, and C. Ortiz de Solorzano. Combination strategies in multi-atlas image segmentation:&lt;br /&gt;
Application to brain MR data. IEEE Tran. Med. Imaging, 28(8):1266 – 1277, 2009.&lt;br /&gt;
&lt;br /&gt;
[2] R.A. Heckemann, J.V. Hajnal, P. Aljabar, D. Rueckert, and A. Hammers. Automatic anatomical brain MRI segmentation&lt;br /&gt;
combining label propagation and decision fusion. Neuroimage, 33(1):115–126, 2006.&lt;br /&gt;
&lt;br /&gt;
[3] T. Rohlfing, R. Brandt, R. Menzel, and C.R. Maurer. Evaluation of atlas selection strategies for atlas-based image&lt;br /&gt;
segmentation with application to confocal microscopy images of bee brains. NeuroImage, 21(4):1428–1442, 2004.&lt;br /&gt;
&lt;br /&gt;
[4] Freesurfer Wiki. http://surfer.nmr.mgh.harvard.edu.&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:NonparametricSegmentation&amp;diff=42516</id>
		<title>Projects:NonparametricSegmentation</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:NonparametricSegmentation&amp;diff=42516"/>
		<updated>2009-09-10T19:25:59Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;=Introduction=&lt;br /&gt;
&lt;br /&gt;
We propose a non-parametric, probabilistic model for the automatic segmentation of medical images, given a training set of images and corresponding label maps. The resulting inference algorithms we develop rely on pairwise registrations between the test image and individual training images. The training labels are then transferred to the test image and fused to compute a final segmentation of the test subject. Label fusion methods have been shown to yield accurate segmentation, since the use&lt;br /&gt;
of multiple registrations captures greater inter-subject anatomical variability and improves robustness against occasional registration failures, cf. [1,2,3]. To the best of our knowledge, this project investigates the first comprehensive probabilistic framework that rigorously motivates label fusion as a segmentation approach. The proposed framework allows us to compare different label fusion algorithms theoretically and practically. In particular, recent label fusion or multi-atlas segmentation algorithms are interpreted as special cases of our framework.&lt;br /&gt;
&lt;br /&gt;
=Application: Brain MRI=&lt;br /&gt;
We instantiate our model in the context of brain MRI segmentation, where whole brain MRI volumes are automatically parcellated into the following anatomical Regions of Interest (ROI): white matter (WM), cerebral cortex(CT), lateral ventricle (LV), hippocampus(HP), amygdala (AM), thalamus (TH), caudate (CA), putamen (PU), palladum (PA). &lt;br /&gt;
The proposed non-parametric model yields four types of label fusion algorithms: &lt;br /&gt;
&lt;br /&gt;
'''(1) Majority Voting:''' The algorithm computes the most frequent propagated labels at each voxel independently. This is a segmentation algorithm commonly used in practice, e.g. [2,3].&lt;br /&gt;
&lt;br /&gt;
'''(2) Local Label Fusion:''' An independent weighted averaging of propagated labels, where the weights vary at each voxel and are a function of the intensity difference between the training image and test image.&lt;br /&gt;
&lt;br /&gt;
'''(3) Semi-Local Label Fusion:''' Propagated labels are fused in a weighted fashion using a variational mean field algorithm. The weights are encouraged to be similar in local patches.&lt;br /&gt;
&lt;br /&gt;
'''(4) Global Label Fusion:''' Propagated labels are fused in a weighted fashion using an Expectation Maximization algorithm. The weights are global, i.e., there is a single weight for each training subject.&lt;br /&gt;
&lt;br /&gt;
The following figure shows an example segmentation obtained via Local Label Fusion.&lt;br /&gt;
&lt;br /&gt;
[[File:Segmentation_example2.png]]&lt;br /&gt;
&lt;br /&gt;
=Experiments=&lt;br /&gt;
We conduct two sets of experiments to validate our framework. In the first set of experiments, we use 39 brain MRI scans – with manually segmented white matter, cerebral cortex, ventricles and subcortical structures – to compare different label fusion algorithms and the widely-used Freesurfer whole-brain segmentation tool [4]. &lt;br /&gt;
&lt;br /&gt;
The following figure shows the Boxplots of Dice scores for all methods: Freesurfer (red), Majority Voting (yellow), Global Weighted Fusion (green), Local Weighted Voting (blue), Semi-local Weighted Fusion (purple).&lt;br /&gt;
&lt;br /&gt;
[[File:DiceScoresPerROI.png]]&lt;br /&gt;
&lt;br /&gt;
Our results indicate that the proposed framework yields more accurate segmentation than Freesurfer and previous label fusion algorithms. In a second experiment, we use brain MRI scans of 304 subjects to demonstrate that the proposed segmentation tool is sufficiently sensitive to robustly detect hippocampal atrophy that foreshadows the onset of Alzheimer’s Disease.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=Literature=&lt;br /&gt;
[1] X. Artaechevarria, A. Munoz-Barrutia, and C. Ortiz de Solorzano. Combination strategies in multi-atlas image segmentation:&lt;br /&gt;
Application to brain MR data. IEEE Tran. Med. Imaging, 28(8):1266 – 1277, 2009.&lt;br /&gt;
&lt;br /&gt;
[2] R.A. Heckemann, J.V. Hajnal, P. Aljabar, D. Rueckert, and A. Hammers. Automatic anatomical brain MRI segmentation&lt;br /&gt;
combining label propagation and decision fusion. Neuroimage, 33(1):115–126, 2006.&lt;br /&gt;
&lt;br /&gt;
[3] T. Rohlfing, R. Brandt, R. Menzel, and C.R. Maurer. Evaluation of atlas selection strategies for atlas-based image&lt;br /&gt;
segmentation with application to confocal microscopy images of bee brains. NeuroImage, 21(4):1428–1442, 2004.&lt;br /&gt;
&lt;br /&gt;
[4] Freesurfer Wiki. http://surfer.nmr.mgh.harvard.edu.&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:NonparametricSegmentation&amp;diff=42511</id>
		<title>Projects:NonparametricSegmentation</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:NonparametricSegmentation&amp;diff=42511"/>
		<updated>2009-09-10T19:23:38Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: /* Application: Brain MRI */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;=Introduction=&lt;br /&gt;
&lt;br /&gt;
We propose a non-parametric, probabilistic model for the automatic segmentation of medical images, given a training set of images and corresponding label maps. The resulting inference algorithms we develop rely on pairwise registrations between the test image and individual training images. The training labels are then transferred to the test image and fused to compute a final segmentation of the test subject. Label fusion methods have been shown to yield accurate segmentation, since the use&lt;br /&gt;
of multiple registrations captures greater inter-subject anatomical variability and improves robustness against occasional registration failures, cf. [1,2,3]. To the best of our knowledge, this project investigates the first comprehensive probabilistic framework that rigorously motivates label fusion as a segmentation approach. The proposed framework allows us to compare different label fusion algorithms theoretically and practically. In particular, recent label fusion or multi-atlas segmentation algorithms are interpreted as special cases of our framework.&lt;br /&gt;
&lt;br /&gt;
=Application: Brain MRI=&lt;br /&gt;
We instantiate our model in the context of brain MRI segmentation, where whole brain MRI volumes are automatically parcellated into the following anatomical Regions of Interest (ROI): white matter (WM), cerebral cortex(CT), lateral ventricle (LV), hippocampus(HP), amygdala (AM), thalamus (TH), caudate (CA), putamen (PU), palladum (PA). &lt;br /&gt;
The proposed non-parametric model yields four types of label fusion algorithms: &lt;br /&gt;
&lt;br /&gt;
'''(1) Majority Voting:''' The algorithm computes the most frequent propagated labels at each voxel independently. This is a segmentation algorithm commonly used in practice, e.g. [2,3].&lt;br /&gt;
&lt;br /&gt;
'''(2) Local Label Fusion:''' An independent weighted averaging of propagated labels, where the weights vary at each voxel and are a function of the intensity difference between the training image and test image.&lt;br /&gt;
&lt;br /&gt;
'''(3) Semi-Local Label Fusion:''' Propagated labels are fused in a weighted fashion using a variational mean field algorithm. The weights are encouraged to be similar in local patches.&lt;br /&gt;
&lt;br /&gt;
'''(4) Global Label Fusion:''' Propagated labels are fused in a weighted fashion using an Expectation Maximization algorithm. The weights are global, i.e., there is a single weight for each training subject.&lt;br /&gt;
&lt;br /&gt;
The following figure shows an example segmentation obtained via Local Label Fusion.&lt;br /&gt;
&lt;br /&gt;
[[File:Segmentation_example2.png]]&lt;br /&gt;
&lt;br /&gt;
=Experiments=&lt;br /&gt;
We conduct two sets of experiments to validate our framework. In the first set of experiments, we use 39 brain MRI scans – with manually segmented white matter, cerebral cortex, ventricles and subcortical structures – to compare different label fusion algorithms and the widely-used Freesurfer whole-brain segmentation tool. Our results indicate that the proposed framework yields more accurate segmentation than Freesurfer and previous label fusion algorithms. In a second experiment, we use brain MRI scans of 304 subjects to demonstrate that the proposed segmentation tool is sufficiently sensitive to robustly detect hippocampal atrophy that foreshadows the onset of Alzheimer’s Disease.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=Literature=&lt;br /&gt;
[1] X. Artaechevarria, A. Munoz-Barrutia, and C. Ortiz de Solorzano. Combination strategies in multi-atlas image segmentation:&lt;br /&gt;
Application to brain MR data. IEEE Tran. Med. Imaging, 28(8):1266 – 1277, 2009.&lt;br /&gt;
&lt;br /&gt;
[2] R.A. Heckemann, J.V. Hajnal, P. Aljabar, D. Rueckert, and A. Hammers. Automatic anatomical brain MRI segmentation&lt;br /&gt;
combining label propagation and decision fusion. Neuroimage, 33(1):115–126, 2006.&lt;br /&gt;
&lt;br /&gt;
[3] T. Rohlfing, R. Brandt, R. Menzel, and C.R. Maurer. Evaluation of atlas selection strategies for atlas-based image&lt;br /&gt;
segmentation with application to confocal microscopy images of bee brains. NeuroImage, 21(4):1428–1442, 2004.&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:NonparametricSegmentation&amp;diff=42510</id>
		<title>Projects:NonparametricSegmentation</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:NonparametricSegmentation&amp;diff=42510"/>
		<updated>2009-09-10T19:22:31Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;=Introduction=&lt;br /&gt;
&lt;br /&gt;
We propose a non-parametric, probabilistic model for the automatic segmentation of medical images, given a training set of images and corresponding label maps. The resulting inference algorithms we develop rely on pairwise registrations between the test image and individual training images. The training labels are then transferred to the test image and fused to compute a final segmentation of the test subject. Label fusion methods have been shown to yield accurate segmentation, since the use&lt;br /&gt;
of multiple registrations captures greater inter-subject anatomical variability and improves robustness against occasional registration failures, cf. [1,2,3]. To the best of our knowledge, this project investigates the first comprehensive probabilistic framework that rigorously motivates label fusion as a segmentation approach. The proposed framework allows us to compare different label fusion algorithms theoretically and practically. In particular, recent label fusion or multi-atlas segmentation algorithms are interpreted as special cases of our framework.&lt;br /&gt;
&lt;br /&gt;
=Application: Brain MRI=&lt;br /&gt;
We instantiate our model in the context of brain MRI segmentation, where whole brain MRI volumes are automatically parcellated into the following anatomical Regions of Interest (ROI): white matter (WM), cerebral cortex(CT), lateral ventricle (LV), hippocampus(HP), amygdala (AM), thalamus (TH), caudate (CA), putamen (PU), palladum (PA). &lt;br /&gt;
The proposed non-parametric model yields four types of label fusion algorithms: &lt;br /&gt;
&lt;br /&gt;
'''(1) Majority Voting:''' The algorithm computes the most frequent propagated labels at each voxel independently.&lt;br /&gt;
&lt;br /&gt;
'''(2) Local Label Fusion:''' An independent weighted averaging of propagated labels, where the weights vary at each voxel and are a function of the intensity difference between the training image and test image.&lt;br /&gt;
&lt;br /&gt;
'''(3) Semi-Local Label Fusion:''' Propagated labels are fused in a weighted fashion using a variational mean field algorithm. The weights are encouraged to be similar in local patches.&lt;br /&gt;
&lt;br /&gt;
'''(4) Global Label Fusion:''' Propagated labels are fused in a weighted fashion using an Expectation Maximization algorithm. The weights are global, i.e., there is a single weight for each training subject.&lt;br /&gt;
&lt;br /&gt;
The following figure shows an example segmentation obtained via Local Label Fusion.&lt;br /&gt;
&lt;br /&gt;
[[File:Segmentation_example2.png]]&lt;br /&gt;
&lt;br /&gt;
=Experiments=&lt;br /&gt;
We conduct two sets of experiments to validate our framework. In the first set of experiments, we use 39 brain MRI scans – with manually segmented white matter, cerebral cortex, ventricles and subcortical structures – to compare different label fusion algorithms and the widely-used Freesurfer whole-brain segmentation tool. Our results indicate that the proposed framework yields more accurate segmentation than Freesurfer and previous label fusion algorithms. In a second experiment, we use brain MRI scans of 304 subjects to demonstrate that the proposed segmentation tool is sufficiently sensitive to robustly detect hippocampal atrophy that foreshadows the onset of Alzheimer’s Disease.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=Literature=&lt;br /&gt;
[1] X. Artaechevarria, A. Munoz-Barrutia, and C. Ortiz de Solorzano. Combination strategies in multi-atlas image segmentation:&lt;br /&gt;
Application to brain MR data. IEEE Tran. Med. Imaging, 28(8):1266 – 1277, 2009.&lt;br /&gt;
&lt;br /&gt;
[2] R.A. Heckemann, J.V. Hajnal, P. Aljabar, D. Rueckert, and A. Hammers. Automatic anatomical brain MRI segmentation&lt;br /&gt;
combining label propagation and decision fusion. Neuroimage, 33(1):115–126, 2006.&lt;br /&gt;
&lt;br /&gt;
[3] T. Rohlfing, R. Brandt, R. Menzel, and C.R. Maurer. Evaluation of atlas selection strategies for atlas-based image&lt;br /&gt;
segmentation with application to confocal microscopy images of bee brains. NeuroImage, 21(4):1428–1442, 2004.&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:NonparametricSegmentation&amp;diff=42509</id>
		<title>Projects:NonparametricSegmentation</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:NonparametricSegmentation&amp;diff=42509"/>
		<updated>2009-09-10T19:22:17Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;=Introduction=&lt;br /&gt;
&lt;br /&gt;
We propose a non-parametric, probabilistic model for the automatic segmentation of medical images, given a training set of images and corresponding label maps. The resulting inference algorithms we develop rely on pairwise registrations between the test image and individual training images. The training labels are then transferred to the test image and fused to compute a final segmentation of the test subject. Label fusion methods have been shown to yield accurate segmentation, since the use&lt;br /&gt;
of multiple registrations captures greater inter-subject anatomical variability and improves robustness against occasional registration failures, cf. [1,2,3]. To the best of our knowledge, this project investigates the first comprehensive probabilistic framework that rigorously motivates label fusion as a segmentation approach. The proposed framework allows us to compare different label fusion algorithms theoretically and practically. In particular, recent label fusion or multi-atlas segmentation algorithms are interpreted as special cases of our framework.&lt;br /&gt;
&lt;br /&gt;
=Application: Brain MRI=&lt;br /&gt;
We instantiate our model in the context of brain MRI segmentation, where whole brain MRI volumes are automatically parcellated into the following anatomical Regions of Interest (ROI): white matter (WM), cerebral cortex(CT), lateral ventricle (LV), hippocampus(HP), amygdala (AM), thalamus (TH), caudate (CA), putamen (PU), palladum (PA). &lt;br /&gt;
The proposed non-parametric model yields four types of label fusion algorithms: &lt;br /&gt;
&lt;br /&gt;
'''(1) Majority Voting:''' The algorithm computes the most frequent propagated labels at each voxel independently.&lt;br /&gt;
&lt;br /&gt;
'''(2) Local Label Fusion:''' An independent weighted averaging of propagated labels, where the weights vary at each voxel and are a function of the intensity difference between the training image and test image.&lt;br /&gt;
&lt;br /&gt;
'''(3) Semi-Local Label Fusion:''' Propagated labels are fused in a weighted fashion using a variational mean field algorithm. The weights are encouraged to be similar in local patches.&lt;br /&gt;
&lt;br /&gt;
'''(4) Global Label Fusion:''' Propagated labels are fused in a weighted fashion using an Expectation Maximization algorithm. The weights are global, i.e., there is a single weight for each training subject.&lt;br /&gt;
&lt;br /&gt;
The following figure shows an example segmentation obtained via Local Label Fusion.&lt;br /&gt;
[[File:Segmentation_example2.png]]&lt;br /&gt;
&lt;br /&gt;
=Experiments=&lt;br /&gt;
We conduct two sets of experiments to validate our framework. In the first set of experiments, we use 39 brain MRI scans – with manually segmented white matter, cerebral cortex, ventricles and subcortical structures – to compare different label fusion algorithms and the widely-used Freesurfer whole-brain segmentation tool. Our results indicate that the proposed framework yields more accurate segmentation than Freesurfer and previous label fusion algorithms. In a second experiment, we use brain MRI scans of 304 subjects to demonstrate that the proposed segmentation tool is sufficiently sensitive to robustly detect hippocampal atrophy that foreshadows the onset of Alzheimer’s Disease.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=Literature=&lt;br /&gt;
[1] X. Artaechevarria, A. Munoz-Barrutia, and C. Ortiz de Solorzano. Combination strategies in multi-atlas image segmentation:&lt;br /&gt;
Application to brain MR data. IEEE Tran. Med. Imaging, 28(8):1266 – 1277, 2009.&lt;br /&gt;
&lt;br /&gt;
[2] R.A. Heckemann, J.V. Hajnal, P. Aljabar, D. Rueckert, and A. Hammers. Automatic anatomical brain MRI segmentation&lt;br /&gt;
combining label propagation and decision fusion. Neuroimage, 33(1):115–126, 2006.&lt;br /&gt;
&lt;br /&gt;
[3] T. Rohlfing, R. Brandt, R. Menzel, and C.R. Maurer. Evaluation of atlas selection strategies for atlas-based image&lt;br /&gt;
segmentation with application to confocal microscopy images of bee brains. NeuroImage, 21(4):1428–1442, 2004.&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=File:HippocampalVolume.png&amp;diff=42508</id>
		<title>File:HippocampalVolume.png</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=File:HippocampalVolume.png&amp;diff=42508"/>
		<updated>2009-09-10T19:21:21Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=File:DiceScoresPerROI.png&amp;diff=42507</id>
		<title>File:DiceScoresPerROI.png</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=File:DiceScoresPerROI.png&amp;diff=42507"/>
		<updated>2009-09-10T19:20:54Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: Dice scores per ROI&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Dice scores per ROI&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=File:DiceScoresAverage.png&amp;diff=42505</id>
		<title>File:DiceScoresAverage.png</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=File:DiceScoresAverage.png&amp;diff=42505"/>
		<updated>2009-09-10T19:20:10Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: Average Dice Score Comparison (SNIP vs. FreeSurfer)&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Average Dice Score Comparison (SNIP vs. FreeSurfer)&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:NonparametricSegmentation&amp;diff=42502</id>
		<title>Projects:NonparametricSegmentation</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:NonparametricSegmentation&amp;diff=42502"/>
		<updated>2009-09-10T19:19:07Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;=Introduction=&lt;br /&gt;
&lt;br /&gt;
We propose a non-parametric, probabilistic model for the automatic segmentation of medical images, given a training set of images and corresponding label maps. The resulting inference algorithms we develop rely on pairwise registrations between the test image and individual training images. The training labels are then transferred to the test image and fused to compute a final segmentation of the test subject. Label fusion methods have been shown to yield accurate segmentation, since the use&lt;br /&gt;
of multiple registrations captures greater inter-subject anatomical variability and improves robustness against occasional registration failures, cf. [1,2,3]. To the best of our knowledge, this project investigates the first comprehensive probabilistic framework that rigorously motivates label fusion as a segmentation approach. The proposed framework allows us to compare different label fusion algorithms theoretically and practically. In particular, recent label fusion or multi-atlas segmentation algorithms are interpreted as special cases of our framework.&lt;br /&gt;
&lt;br /&gt;
=Application: Brain MRI=&lt;br /&gt;
We instantiate our model in the context of brain MRI segmentation, where whole brain MRI volumes are automatically parcellated into the following anatomical Regions of Interest (ROI): white matter (WM), cerebral cortex(CT), lateral ventricle (LV), hippocampus(HP), amygdala (AM), thalamus (TH), caudate (CA), putamen (PU), palladum (PA). &lt;br /&gt;
The proposed non-parametric model yields four types of label fusion algorithms: &lt;br /&gt;
&lt;br /&gt;
'''(1) Majority Voting:''' The algorithm computes the most frequent propagated labels at each voxel independently.&lt;br /&gt;
&lt;br /&gt;
'''(2) Local Label Fusion:''' An independent weighted averaging of propagated labels, where the weights vary at each voxel and are a function of the intensity difference between the training image and test image.&lt;br /&gt;
&lt;br /&gt;
'''(3) Semi-Local Label Fusion:''' Propagated labels are fused in a weighted fashion using a variational mean field algorithm. The weights are encouraged to be similar in local patches.&lt;br /&gt;
&lt;br /&gt;
'''(4) Global Label Fusion:''' Propagated labels are fused in a weighted fashion using an Expectation Maximization algorithm. The weights are global, i.e., there is a single weight for each training subject.&lt;br /&gt;
&lt;br /&gt;
The following figure shows an example segmentation obtained via Local Label Fusion.&lt;br /&gt;
&lt;br /&gt;
=Experiments=&lt;br /&gt;
We conduct two sets of experiments to validate our framework. In the first set of experiments, we use 39 brain MRI scans – with manually segmented white matter, cerebral cortex, ventricles and subcortical structures – to compare different label fusion algorithms and the widely-used Freesurfer whole-brain segmentation tool. Our results indicate that the proposed framework yields more accurate segmentation than Freesurfer and previous label fusion algorithms. In a second experiment, we use brain MRI scans of 304 subjects to demonstrate that the proposed segmentation tool is sufficiently sensitive to robustly detect hippocampal atrophy that foreshadows the onset of Alzheimer’s Disease.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=Literature=&lt;br /&gt;
[1] X. Artaechevarria, A. Munoz-Barrutia, and C. Ortiz de Solorzano. Combination strategies in multi-atlas image segmentation:&lt;br /&gt;
Application to brain MR data. IEEE Tran. Med. Imaging, 28(8):1266 – 1277, 2009.&lt;br /&gt;
&lt;br /&gt;
[2] R.A. Heckemann, J.V. Hajnal, P. Aljabar, D. Rueckert, and A. Hammers. Automatic anatomical brain MRI segmentation&lt;br /&gt;
combining label propagation and decision fusion. Neuroimage, 33(1):115–126, 2006.&lt;br /&gt;
&lt;br /&gt;
[3] T. Rohlfing, R. Brandt, R. Menzel, and C.R. Maurer. Evaluation of atlas selection strategies for atlas-based image&lt;br /&gt;
segmentation with application to confocal microscopy images of bee brains. NeuroImage, 21(4):1428–1442, 2004.&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:NonparametricSegmentation&amp;diff=42497</id>
		<title>Projects:NonparametricSegmentation</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:NonparametricSegmentation&amp;diff=42497"/>
		<updated>2009-09-10T19:17:59Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;=Introduction=&lt;br /&gt;
&lt;br /&gt;
We propose a non-parametric, probabilistic model for the automatic segmentation of medical images, given a training set of images and corresponding label maps. The resulting inference algorithms we develop rely on pairwise registrations between the test image and individual training images. The training labels are then transferred to the test image and fused to compute a final segmentation of the test subject. Label fusion methods have been shown to yield accurate segmentation, since the use&lt;br /&gt;
of multiple registrations captures greater inter-subject anatomical variability and improves robustness against occasional registration failures, cf. [1,2,3]. To the best of our knowledge, this project investigates the first comprehensive probabilistic framework that rigorously motivates label fusion as a segmentation approach. The proposed framework allows us to compare different label fusion algorithms theoretically and practically. In particular, recent label fusion or multi-atlas segmentation algorithms are interpreted as special cases of our framework.&lt;br /&gt;
&lt;br /&gt;
=Application: Brain MRI=&lt;br /&gt;
We instantiate our model in the context of brain MRI segmentation, where whole brain MRI volumes are automatically parcellated into the following anatomical Regions of Interest (ROI): white matter (WM), cerebral cortex(CT), lateral ventricle (LV), hippocampus(HP), amygdala (AM), thalamus (TH), caudate (CA), putamen (PU), palladum (PA). &lt;br /&gt;
The proposed non-parametric model yields four types of label fusion algorithms: &lt;br /&gt;
&lt;br /&gt;
(1) Majority Voting: The algorithm computes the most frequent propagated labels at each voxel independently.&lt;br /&gt;
&lt;br /&gt;
(2) Local Label Fusion: An independent weighted averaging of propagated labels, where the weights vary at each voxel and are a function of the intensity difference between the training image and test image.&lt;br /&gt;
&lt;br /&gt;
(3) Semi-Local Label Fusion: Propagated labels are fused in a weighted fashion using a variational mean field algorithm. The weights are encouraged to be similar in local patches.&lt;br /&gt;
&lt;br /&gt;
(4) Global Label Fusion: Propagated labels are fused in a weighted fashion using an Expectation Maximization algorithm. The weights are global, i.e., there is a single weight for each training subject.&lt;br /&gt;
&lt;br /&gt;
The following figure shows an example segmentation obtained via Local Label Fusion.&lt;br /&gt;
&lt;br /&gt;
=Experiments=&lt;br /&gt;
We conduct two sets of experiments to validate our framework. In the first set of experiments, we use 39 brain MRI scans – with manually segmented white matter, cerebral cortex, ventricles and subcortical structures – to compare different label fusion algorithms and the widely-used Freesurfer whole-brain segmentation tool. Our results indicate that the proposed framework yields more accurate segmentation than Freesurfer and previous label fusion algorithms. In a second experiment, we use brain MRI scans of 304 subjects to demonstrate that the proposed segmentation tool is sufficiently sensitive to robustly detect hippocampal atrophy that foreshadows the onset of Alzheimer’s Disease.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=Literature=&lt;br /&gt;
[1] X. Artaechevarria, A. Munoz-Barrutia, and C. Ortiz de Solorzano. Combination strategies in multi-atlas image segmentation:&lt;br /&gt;
Application to brain MR data. IEEE Tran. Med. Imaging, 28(8):1266 – 1277, 2009.&lt;br /&gt;
&lt;br /&gt;
[2] R.A. Heckemann, J.V. Hajnal, P. Aljabar, D. Rueckert, and A. Hammers. Automatic anatomical brain MRI segmentation&lt;br /&gt;
combining label propagation and decision fusion. Neuroimage, 33(1):115–126, 2006.&lt;br /&gt;
&lt;br /&gt;
[3] T. Rohlfing, R. Brandt, R. Menzel, and C.R. Maurer. Evaluation of atlas selection strategies for atlas-based image&lt;br /&gt;
segmentation with application to confocal microscopy images of bee brains. NeuroImage, 21(4):1428–1442, 2004.&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:NonparametricSegmentation&amp;diff=42469</id>
		<title>Projects:NonparametricSegmentation</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:NonparametricSegmentation&amp;diff=42469"/>
		<updated>2009-09-10T18:57:12Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;=Introduction=&lt;br /&gt;
&lt;br /&gt;
We propose a non-parametric, probabilistic model for the automatic segmentation of medical images, given a training set of images and corresponding label maps. The resulting inference algorithms we develop rely on pairwise registrations between the test image and individual training images. The training labels are then transferred to the test image and fused to compute a final segmentation of the test subject. Label fusion methods have been shown to yield accurate segmentation, since the use&lt;br /&gt;
of multiple registrations captures greater inter-subject anatomical variability and improves robustness against occasional registration failures, cf. [1,2,3]. To the best of our knowledge, this project presents the first comprehensive probabilistic framework that rigorously motivates label fusion as a segmentation approach. The proposed framework allows us to compare different label fusion algorithms theoretically and practically. In particular, recent label fusion or multi-atlas segmentation algorithms are interpreted as special cases of our framework.&lt;br /&gt;
&lt;br /&gt;
We conduct two sets of experiments to validate our framework. In the first set of experiments, we use 39 brain MRI scans – with manually segmented white matter, cerebral cortex, ventricles and subcortical structures – to compare different label fusion algorithms and the widely-used Freesurfer whole-brain segmentation tool. Our results indicate that the proposed framework yields more accurate segmentation than Freesurfer and previous label fusion algorithms. In a second experiment, we use brain MRI scans of 304 subjects to demonstrate that the proposed segmentation tool is sufficiently sensitive to robustly detect hippocampal atrophy that foreshadows the onset of Alzheimer’s Disease.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=Literature=&lt;br /&gt;
[1] X. Artaechevarria, A. Munoz-Barrutia, and C. Ortiz de Solorzano. Combination strategies in multi-atlas image segmentation:&lt;br /&gt;
Application to brain MR data. IEEE Tran. Med. Imaging, 28(8):1266 – 1277, 2009.&lt;br /&gt;
&lt;br /&gt;
[2] R.A. Heckemann, J.V. Hajnal, P. Aljabar, D. Rueckert, and A. Hammers. Automatic anatomical brain MRI segmentation&lt;br /&gt;
combining label propagation and decision fusion. Neuroimage, 33(1):115–126, 2006.&lt;br /&gt;
&lt;br /&gt;
[3] T. Rohlfing, R. Brandt, R. Menzel, and C.R. Maurer. Evaluation of atlas selection strategies for atlas-based image&lt;br /&gt;
segmentation with application to confocal microscopy images of bee brains. NeuroImage, 21(4):1428–1442, 2004.&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:NonparametricSegmentation&amp;diff=42464</id>
		<title>Projects:NonparametricSegmentation</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:NonparametricSegmentation&amp;diff=42464"/>
		<updated>2009-09-10T18:53:42Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: /* Introduction */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;=Introduction=&lt;br /&gt;
&lt;br /&gt;
We propose a non-parametric, probabilistic model for the automatic segmentation of medical images, given a training set of images and corresponding label maps. The resulting inference algorithms we develop rely on pairwise registrations between the test image and individual training images. The training labels are then transferred to the test image and fused to compute a final segmentation of the test subject. Label fusion methods have been shown to yield accurate segmentation, since the use&lt;br /&gt;
of multiple registrations captures greater inter-subject anatomical variability and improves robustness against occasional registration failures, cf. [1,2,3]. To the best of our knowledge, this project presents the first comprehensive probabilistic framework that rigorously motivates label fusion as a segmentation approach. The proposed framework allows us to compare different label fusion algorithms theoretically and practically. In particular, recent label fusion or multi-atlas segmentation algorithms are interpreted as special cases of our framework.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=Literature=&lt;br /&gt;
[1] X. Artaechevarria, A. Munoz-Barrutia, and C. Ortiz de Solorzano. Combination strategies in multi-atlas image segmentation:&lt;br /&gt;
Application to brain MR data. IEEE Tran. Med. Imaging, 28(8):1266 – 1277, 2009.&lt;br /&gt;
&lt;br /&gt;
[2] R.A. Heckemann, J.V. Hajnal, P. Aljabar, D. Rueckert, and A. Hammers. Automatic anatomical brain MRI segmentation&lt;br /&gt;
combining label propagation and decision fusion. Neuroimage, 33(1):115–126, 2006.&lt;br /&gt;
&lt;br /&gt;
[3] T. Rohlfing, R. Brandt, R. Menzel, and C.R. Maurer. Evaluation of atlas selection strategies for atlas-based image&lt;br /&gt;
segmentation with application to confocal microscopy images of bee brains. NeuroImage, 21(4):1428–1442, 2004.&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:NonparametricSegmentation&amp;diff=42462</id>
		<title>Projects:NonparametricSegmentation</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:NonparametricSegmentation&amp;diff=42462"/>
		<updated>2009-09-10T18:52:58Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: /* Introduction */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;=Introduction=&lt;br /&gt;
&lt;br /&gt;
We propose a non-parametric, probabilistic model for the automatic segmentation of medical images, given a training set of images and corresponding label maps. The resulting inference algorithms we develop rely on pairwise registrations between the test image and individual training images. The training labels are then transferred to the test image and fused to compute a final segmentation of the test subject. Label fusion methods have been shown to yield accurate segmentation, since the use&lt;br /&gt;
of multiple registrations captures greater inter-subject anatomical variability and improves robustness against occasional registration failures, cf. [1,2,3]. To the best of our knowledge, this project presents the first comprehensive probabilistic framework that rigorously motivates label fusion as a segmentation approach. The proposed framework allows us to compare different label fusion algorithms theoretically and practically. In particular, recent label fusion or multi-atlas segmentation algorithms are interpreted as special cases of our framework.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=Literature=&lt;br /&gt;
[1] X. Artaechevarria, A. Munoz-Barrutia, and C. Ortiz de Solorzano. Combination strategies in multi-atlas image segmentation:&lt;br /&gt;
Application to brain MR data. IEEE Tran. Med. Imaging, 28(8):1266 – 1277, 2009.&lt;br /&gt;
[2] R.A. Heckemann, J.V. Hajnal, P. Aljabar, D. Rueckert, and A. Hammers. Automatic anatomical brain MRI segmentation&lt;br /&gt;
combining label propagation and decision fusion. Neuroimage, 33(1):115–126, 2006.&lt;br /&gt;
[3] T. Rohlfing, R. Brandt, R. Menzel, and C.R. Maurer. Evaluation of atlas selection strategies for atlas-based image&lt;br /&gt;
segmentation with application to confocal microscopy images of bee brains. NeuroImage, 21(4):1428–1442, 2004.&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:NonparametricSegmentation&amp;diff=42458</id>
		<title>Projects:NonparametricSegmentation</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:NonparametricSegmentation&amp;diff=42458"/>
		<updated>2009-09-10T18:50:58Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: /* Introduction */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;=Introduction=&lt;br /&gt;
&lt;br /&gt;
We propose a non-parametric, probabilistic model for the automatic segmentation of medical images, given a training set of images and corresponding label maps. The resulting inference algorithms we develop rely on pairwise registrations between the test image and individual training images. The training labels are then transferred to the test image and fused to compute a final segmentation of the test subject. Label fusion methods have been shown to yield accurate segmentation, since the use&lt;br /&gt;
of multiple registrations captures greater inter-subject anatomical variability and improves robustness against occasional registration failures. To the best of our knowledge, this project presents the first comprehensive probabilistic framework that rigorously motivates label fusion as a segmentation approach. The proposed framework allows us to compare different label fusion algorithms theoretically and practically. In particular, recent label fusion or multi-atlas segmentation algorithms are interpreted as special cases of our framework.&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:NonparametricSegmentation&amp;diff=42455</id>
		<title>Projects:NonparametricSegmentation</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:NonparametricSegmentation&amp;diff=42455"/>
		<updated>2009-09-10T18:50:22Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: /* Introduction and Background */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;=Introduction=&lt;br /&gt;
&lt;br /&gt;
We propose a non-parametric, probabilistic model for the automatic segmentation of medical images, given a training set of images and corresponding label maps. The resulting inference algorithms we develop rely on pairwise registrations between the test image and individual training images. The training labels are then transferred to the test image and fused to compute a final segmentation of the test subject. Label fusion methods have been shown to yield accurate segmentation, since the use&lt;br /&gt;
of multiple registrations captures greater inter-subject anatomical variability and improves robustness against occasional registration failures. To the best of our knowledge, this manuscript presents the first comprehensive probabilistic framework that rigorously motivates label fusion as a segmentation approach. The proposed framework allows us to compare different label fusion algorithms theoretically and practically. In particular, recent label fusion or multi-atlas segmentation algorithms are interpreted as special cases of our framework.&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:NonparametricSegmentation&amp;diff=42452</id>
		<title>Projects:NonparametricSegmentation</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:NonparametricSegmentation&amp;diff=42452"/>
		<updated>2009-09-10T18:47:39Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;=Introduction and Background=&lt;br /&gt;
&lt;br /&gt;
We propose a non-parametric, probabilistic model for the automatic segmentation of medical images, given a training set of images and corresponding label maps. The resulting inference algorithms we develop rely on pairwise registrations between the test image and individual training images. The training labels are then transferred to the test image and fused to compute a final segmentation of the test subject.&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:NonparametricSegmentation&amp;diff=42450</id>
		<title>Projects:NonparametricSegmentation</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:NonparametricSegmentation&amp;diff=42450"/>
		<updated>2009-09-10T18:46:29Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: Created page with 'We propose a non-parametric, probabilistic model for the automatic segmentation of medical images, given a training set of images and corresponding label maps. The resulting infe…'&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;We propose a non-parametric, probabilistic model for the automatic segmentation of medical images, given a training set of images and corresponding label maps. The resulting inference algorithms we develop rely on pairwise registrations between the test image and individual training images. The training labels are then transferred to the test image and fused to compute a final segmentation of the test subject.&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Algorithm:MIT&amp;diff=42445</id>
		<title>Algorithm:MIT</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Algorithm:MIT&amp;diff=42445"/>
		<updated>2009-09-10T18:44:01Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: /* MIT Projects */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; Back to [[Algorithm:Main|NA-MIC Algorithms]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
= Overview of MIT Algorithms (PI: Polina Golland) =&lt;br /&gt;
&lt;br /&gt;
Our group seeks to model statistical variability of anatomy and function across subjects and between populations and to utilize computational models of such variability to improve predictions for individual subjects, as well as characterize populations. Our long-term goal is to develop methods for joint modeling of anatomy and function and to apply them in clinical and scientific studies. We work primarily with anatomical, DTI and fMRI images. We actively contribute implementations of our algorithms to the NAMIC-kit.&lt;br /&gt;
&lt;br /&gt;
= MIT Projects =&lt;br /&gt;
&lt;br /&gt;
{| cellpadding=&amp;quot;10&amp;quot; style=&amp;quot;text-align:left;&amp;quot;&lt;br /&gt;
|| [[Image:Segmentation_example2.png|250px]]&lt;br /&gt;
||&lt;br /&gt;
&lt;br /&gt;
== [[Projects:NonparametricSegmentation| Nonparametric Models for Supervised Image Segmentation]] ==&lt;br /&gt;
&lt;br /&gt;
We propose a non-parametric, probabilistic model for the automatic segmentation of medical images,&lt;br /&gt;
given a training set of images and corresponding label maps. The resulting inference algorithms we&lt;br /&gt;
develop rely on pairwise registrations between the test image and individual training images. The&lt;br /&gt;
training labels are then transferred to the test image and fused to compute a final segmentation of&lt;br /&gt;
the test subject. [[Projects:NonparametricSegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; Supervised Nonparametric Image Parcellation, M.R. Sabuncu, B.T. Thomas Yeo, K. Van Leemput, B. Fischl, and P. Golland. To appear in Proceedings of the International Conference on Medical Image Computing and Computer Assisted Intervention (MICCAI), 2009.&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; Nonparametric Mixture Models for Supervised Image Parcellation, M.R. Sabuncu, &lt;br /&gt;
B.T.T. Yeo, K. Van Leemput, B. Fischl, and P. Golland. To be presented at PMMIA Workshop at MICCAI 2009.   &lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{| cellpadding=&amp;quot;10&amp;quot; style=&amp;quot;text-align:left;&amp;quot;&lt;br /&gt;
| style=&amp;quot;width:15%&amp;quot; | [[Image:MITHippocampalSubfieldSegmentation.png|250px]]&lt;br /&gt;
| style=&amp;quot;width:85%&amp;quot; |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:BayesianMRSegmentation| Bayesian Segmentation of MRI Images]] ==&lt;br /&gt;
&lt;br /&gt;
In this project we develop and validate a method for fully automated segmentation of the subfields of the hippocampus in ultra-high resolution in vivo MRI. [[Projects:HippocampalSubfieldSegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; Automated Segmentation of Hippocampal Subﬁelds from Ultra-High Resolution In Vivo MRI, K. Van Leemput, A. Bakkour, T. Benner, G. Wiggins, L.L. Wald, J. Augustinack, B.C. Dickerson, P. Golland, and B. Fischl. Hippocampus. Accepted for Publication, 2009.&lt;br /&gt;
&lt;br /&gt;
Encoding Probabilistic Atlases Using Bayesian Inference, K. Van Leemput. IEEE Transactions on Medical Imaging. Accepted for Publication, 2009.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:ICluster_templates.gif|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:MultimodalAtlas|Multimodal Atlas]] ==&lt;br /&gt;
&lt;br /&gt;
In this work, we propose and investigate an algorithm that jointly co-registers a collection of images while computing multiple templates. The algorithm, called '''iCluster''', is used to compute multiple atlases for a given population.&lt;br /&gt;
[[Projects:MultimodalAtlas|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; Image-driven Population Analysis through Mixture-Modeling, M.R. Sabuncu, S.K. Balci, M.E. Shenton and P. Golland. IEEE Transactions on Medical Imaging. Accepted for Publication, 2009.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:CoordinateChart.png|250px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:SphericalDemons|Spherical Demons: Fast Surface Registration]] ==&lt;br /&gt;
&lt;br /&gt;
We present the fast Spherical Demons algorithm for registering two spherical images. By exploiting spherical vector spline interpolation theory, we show that a large class of regularizers for the modified demons objective function can be efficiently approximated on the sphere using convolution. Based on the one parameter subgroups of diffeomorphisms, [[Projects:SphericalDemons|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; B.T.T. Yeo, M. Sabuncu, T. Vercauteren, N. Ayache, B. Fischl, P. Golland. Spherical Demons: Fast Surface Registration. MICCAI, volume 5241 of LNCS, 745--753, 2008.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:JointRegSeg.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:RegistrationRegularization|Optimal Atlas Regularization in Image Segmentation]] ==&lt;br /&gt;
&lt;br /&gt;
We propose a unified framework for computing atlases from manually labeled data sets at various degrees of “sharpness” and the joint registration and segmentation of a new brain with these atlases. Using this framework, we investigate the tradeoff between warp regularization and image ﬁdelity, i.e. the smoothness of the new subject warp and the sharpness of the atlas in a segmentation application.&lt;br /&gt;
[[Projects:RegistrationRegularization|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; B.T.T. Yeo, M.R. Sabuncu, R. Desikan, B. Fischl, P. Golland. Effects of Registration Regularization and Atlas Sharpness on Segmentation Accuracy. Medical Image Analysis, 12(5):603--615, 2008. &lt;br /&gt;
  &lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:epi_correction_small.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:FieldmapFreeDistortionCorrection|Fieldmap-Free EPI Distortion Correction]] ==&lt;br /&gt;
&lt;br /&gt;
In this project we aim to improve the EPI distortion correction algorithms [[Projects:FieldmapFreeDistortionCorrection|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt;  Poynton C., Jenkinson M., Whalen S., Golby A.J., Wells III W. Fieldmap-Free Retrospective Registration and Distortion Correction for EPI-Based Functiona Imaging. MICCAI 2008.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:mit_fmri_clustering_parcellation2_xsub.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:fMRIClustering|fMRI clustering]] ==&lt;br /&gt;
&lt;br /&gt;
In this project we study the application of model-based clustering algorithms in identification of functional connectivity in the brain. [[Projects:fMRIClustering|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; A. Venkataraman, K.R.A. Van Dijk, R.L. Buckner, P. Golland. Exploring Functional Connectivity in fMRI via Clustering. ICASSP 2009. &lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; D. Lashkari, E. Vul, N. Kanwisher, P. Golland. Discovering Structure in the Space of Activation&lt;br /&gt;
Profiles in fMRI. MICCAI 2008. &lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:FoldingSpeedDetection.png|150px|]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeAnalysisWithOvercompleteWavelets|Shape Analysis With Overcomplete Wavelets]] ==&lt;br /&gt;
&lt;br /&gt;
In this work, we extend the Euclidean wavelets to the sphere. The resulting over-complete spherical wavelets are invariant to the rotation of the spherical image parameterization. We apply the over-complete spherical wavelet to cortical folding development [[Projects:ShapeAnalysisWithOvercompleteWavelets|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; B.T.T. Yeo, P. Yu, P.E. Grant, B. Fischl, P. Golland. Shape Analysis with Overcomplete Spherical Wavelets. Proceedings of the International Conference on Medical Image Computing and Computer Assisted Intervention (MICCAI), volume 5241 of LNCS, 468--476, 2008&lt;br /&gt;
&lt;br /&gt;
B.T.T. Yeo, W. Ou, P. Golland. On the Construction of Invertible Filter Banks on the 2-Sphere. Yeo, Ou and Golland. IEEE Transactions on Image Processing. 17(3):283--300. 2008. &lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:Models.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIModeling|Fiber Tract Modeling, Clustering, and Quantitative Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this work is to model the shape of the fiber bundles and use this model description in clustering and statistical analysis of fiber tracts. [[Projects:DTIModeling|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; Mahnaz Maddah, Marek Kubicki, William M. Wells, Carl-Fredrik Westin, Martha E. Shenton and W. Eric L. Grimson, Findings in Schizophrenia by Tract-Oriented DT-MRI Analysis. MICCAI 2008.&lt;br /&gt;
&lt;br /&gt;
M. Maddah, L. Zollei, W. E. L. Grimson, W. M. Wells, Modeling of Anatomical Information in Clustering of White Matter Fiber Trajectories Using Dirichlet Distribution. MMBIA 2008.&lt;br /&gt;
&lt;br /&gt;
M. Maddah, L. Zollei, W. E. L. Grimson, C-F Westin, W. M. Wells, A Mathematical Framework for Incorporating Anatomical Knowledge in DT-MRI Analysis. ISBI 2008.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:TGIt.gif| 150px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:LatentAtlasSegmentation|Joint Segmentation of Image Ensembles via Latent Atlases]] ==&lt;br /&gt;
&lt;br /&gt;
Spatial priors, such as probabilistic atlases, play an important role in MRI segmentation. The atlases are typically generated by averaging manual labels of aligned brain regions across different subjects. However, the availability of comprehensive, reliable and suitable manual segmentations is limited. We therefore propose a joint segmentation of corresponding, aligned structures in the entire population that does not require a probability atlas. [[Projects:LatentAtlasSegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; Joint Segmentation of Image Ensembles via Latent Atlases T. Riklin Raviv, K. Van Leemput, W.M. Wells III and P. Golland, Proceedings of the International Conference on Medical Image Computing and Computer Assisted Intervention (MICCAI), 2009&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:Progress_Registration_Segmentation_Shape.jpg|180px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeBasedSegmentationAndRegistration|Shape Based Segmentation and Registration]] ==&lt;br /&gt;
&lt;br /&gt;
This type of algorithm assigns a tissue type to each voxel in the volume. Incorporating prior shape information biases the label assignment towards contiguous regions that are consistent with the shape model. [[Projects:ShapeBasedSegmentationAndRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:GroupwiseSummary.PNG|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:GroupwiseRegistration|Groupwise Registration]] ==&lt;br /&gt;
&lt;br /&gt;
We extend a previously demonstrated entropy based groupwise registration method to include a free-form deformation model based on B-splines. We provide an efficient implementation using stochastic gradient descents in a multi-resolution setting. We demonstrate the method in application to a set of 50 MRI brain scans and compare the results to a pairwise approach using segmentation labels to evaluate the quality of alignment.&lt;br /&gt;
[[Projects:GroupwiseRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:MIT_DTI_JointSegReg_atlas3D.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIFiberRegistration|Joint Registration and Segmentation of DWI Fiber Tractography]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this work is to jointly register and cluster DWI fiber tracts obtained from a group of subjects. [[Projects:DTIFiberRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:brain.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIClustering|DTI Fiber Clustering and Fiber-Based Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this project is to provide structural description of the white matter architecture as a partition into coherent fiber bundles and clusters, and to use these bundles for quantitative measurement. [[Projects:DTIClustering|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:FMRIEvaluationchart.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:fMRIDetection|fMRI Detection and Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
We are exploring algorithms for improved fMRI detection and interpretation by incorporting spatial priors and anatomical information to guide the detection. [[Projects:fMRIDetection|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:Thalamus_algo_outline.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTISegmentation|DTI-based Segmentation]] ==&lt;br /&gt;
&lt;br /&gt;
Unlike conventional MRI, DTI provides adequate contrast to segment the thalamic nuclei, which are gray matter structures. [[Projects:DTISegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:ConnectivityMap.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIStochasticTractography|Stochastic Tractography]] ==&lt;br /&gt;
&lt;br /&gt;
This work calculates posterior distributions of white matter fiber tract parameters given diffusion observations in a DWI volume.  [[Projects:DTIStochasticTractography|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:HippocampalShapeDifferences.gif|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeAnalysis|Population Analysis of Anatomical Variability]] ==&lt;br /&gt;
&lt;br /&gt;
Our goal is to develop mathematical approaches to modeling anatomical variability within and across populations using tools like local shape descriptors of specific regions of interest and global constellation descriptors of multiple ROI's. [[Projects:ShapeAnalysis|More...]]&lt;br /&gt;
&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Algorithm:MIT&amp;diff=42443</id>
		<title>Algorithm:MIT</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Algorithm:MIT&amp;diff=42443"/>
		<updated>2009-09-10T18:42:17Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: /* MIT Projects */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; Back to [[Algorithm:Main|NA-MIC Algorithms]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
= Overview of MIT Algorithms (PI: Polina Golland) =&lt;br /&gt;
&lt;br /&gt;
Our group seeks to model statistical variability of anatomy and function across subjects and between populations and to utilize computational models of such variability to improve predictions for individual subjects, as well as characterize populations. Our long-term goal is to develop methods for joint modeling of anatomy and function and to apply them in clinical and scientific studies. We work primarily with anatomical, DTI and fMRI images. We actively contribute implementations of our algorithms to the NAMIC-kit.&lt;br /&gt;
&lt;br /&gt;
= MIT Projects =&lt;br /&gt;
&lt;br /&gt;
{| cellpadding=&amp;quot;10&amp;quot; style=&amp;quot;text-align:left;&amp;quot;&lt;br /&gt;
|| [[Image:Segmentation_example2.png|250px]]&lt;br /&gt;
||&lt;br /&gt;
&lt;br /&gt;
== [[Projects:NonparametricSegmentation| Nonparametric Models for Supervised Image Segmentation]] ==&lt;br /&gt;
&lt;br /&gt;
We propose a non-parametric, probabilistic model for the automatic segmentation of medical images,&lt;br /&gt;
given a training set of images and corresponding label maps. The resulting inference algorithms we&lt;br /&gt;
develop rely on pairwise registrations between the test image and individual training images. The&lt;br /&gt;
training labels are then transferred to the test image and fused to compute a final segmentation of&lt;br /&gt;
the test subject. [[Projects:NonparametricSegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; Supervised Nonparametric Image Parcellation, M.R. Sabuncu, B.T. Thomas Yeo, K. Van Leemput, B. Fischl, and P. Golland. To appear in Proceedings of the International Conference on Medical Image Computing and Computer Assisted Intervention (MICCAI), 2009.&lt;br /&gt;
&lt;br /&gt;
Encoding Probabilistic Atlases Using Bayesian Inference, K. Van Leemput. IEEE Transactions on Medical Imaging. Accepted for Publication, 2009.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{| cellpadding=&amp;quot;10&amp;quot; style=&amp;quot;text-align:left;&amp;quot;&lt;br /&gt;
| style=&amp;quot;width:15%&amp;quot; | [[Image:MITHippocampalSubfieldSegmentation.png|250px]]&lt;br /&gt;
| style=&amp;quot;width:85%&amp;quot; |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:BayesianMRSegmentation| Bayesian Segmentation of MRI Images]] ==&lt;br /&gt;
&lt;br /&gt;
In this project we develop and validate a method for fully automated segmentation of the subfields of the hippocampus in ultra-high resolution in vivo MRI. [[Projects:HippocampalSubfieldSegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; Automated Segmentation of Hippocampal Subﬁelds from Ultra-High Resolution In Vivo MRI, K. Van Leemput, A. Bakkour, T. Benner, G. Wiggins, L.L. Wald, J. Augustinack, B.C. Dickerson, P. Golland, and B. Fischl. Hippocampus. Accepted for Publication, 2009.&lt;br /&gt;
&lt;br /&gt;
Encoding Probabilistic Atlases Using Bayesian Inference, K. Van Leemput. IEEE Transactions on Medical Imaging. Accepted for Publication, 2009.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:ICluster_templates.gif|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:MultimodalAtlas|Multimodal Atlas]] ==&lt;br /&gt;
&lt;br /&gt;
In this work, we propose and investigate an algorithm that jointly co-registers a collection of images while computing multiple templates. The algorithm, called '''iCluster''', is used to compute multiple atlases for a given population.&lt;br /&gt;
[[Projects:MultimodalAtlas|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; Image-driven Population Analysis through Mixture-Modeling, M.R. Sabuncu, S.K. Balci, M.E. Shenton and P. Golland. IEEE Transactions on Medical Imaging. Accepted for Publication, 2009.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:CoordinateChart.png|250px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:SphericalDemons|Spherical Demons: Fast Surface Registration]] ==&lt;br /&gt;
&lt;br /&gt;
We present the fast Spherical Demons algorithm for registering two spherical images. By exploiting spherical vector spline interpolation theory, we show that a large class of regularizers for the modified demons objective function can be efficiently approximated on the sphere using convolution. Based on the one parameter subgroups of diffeomorphisms, [[Projects:SphericalDemons|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; B.T.T. Yeo, M. Sabuncu, T. Vercauteren, N. Ayache, B. Fischl, P. Golland. Spherical Demons: Fast Surface Registration. MICCAI, volume 5241 of LNCS, 745--753, 2008.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:JointRegSeg.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:RegistrationRegularization|Optimal Atlas Regularization in Image Segmentation]] ==&lt;br /&gt;
&lt;br /&gt;
We propose a unified framework for computing atlases from manually labeled data sets at various degrees of “sharpness” and the joint registration and segmentation of a new brain with these atlases. Using this framework, we investigate the tradeoff between warp regularization and image ﬁdelity, i.e. the smoothness of the new subject warp and the sharpness of the atlas in a segmentation application.&lt;br /&gt;
[[Projects:RegistrationRegularization|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; B.T.T. Yeo, M.R. Sabuncu, R. Desikan, B. Fischl, P. Golland. Effects of Registration Regularization and Atlas Sharpness on Segmentation Accuracy. Medical Image Analysis, 12(5):603--615, 2008. &lt;br /&gt;
  &lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:epi_correction_small.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:FieldmapFreeDistortionCorrection|Fieldmap-Free EPI Distortion Correction]] ==&lt;br /&gt;
&lt;br /&gt;
In this project we aim to improve the EPI distortion correction algorithms [[Projects:FieldmapFreeDistortionCorrection|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt;  Poynton C., Jenkinson M., Whalen S., Golby A.J., Wells III W. Fieldmap-Free Retrospective Registration and Distortion Correction for EPI-Based Functiona Imaging. MICCAI 2008.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:mit_fmri_clustering_parcellation2_xsub.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:fMRIClustering|fMRI clustering]] ==&lt;br /&gt;
&lt;br /&gt;
In this project we study the application of model-based clustering algorithms in identification of functional connectivity in the brain. [[Projects:fMRIClustering|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; A. Venkataraman, K.R.A. Van Dijk, R.L. Buckner, P. Golland. Exploring Functional Connectivity in fMRI via Clustering. ICASSP 2009. &lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; D. Lashkari, E. Vul, N. Kanwisher, P. Golland. Discovering Structure in the Space of Activation&lt;br /&gt;
Profiles in fMRI. MICCAI 2008. &lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:FoldingSpeedDetection.png|150px|]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeAnalysisWithOvercompleteWavelets|Shape Analysis With Overcomplete Wavelets]] ==&lt;br /&gt;
&lt;br /&gt;
In this work, we extend the Euclidean wavelets to the sphere. The resulting over-complete spherical wavelets are invariant to the rotation of the spherical image parameterization. We apply the over-complete spherical wavelet to cortical folding development [[Projects:ShapeAnalysisWithOvercompleteWavelets|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; B.T.T. Yeo, P. Yu, P.E. Grant, B. Fischl, P. Golland. Shape Analysis with Overcomplete Spherical Wavelets. Proceedings of the International Conference on Medical Image Computing and Computer Assisted Intervention (MICCAI), volume 5241 of LNCS, 468--476, 2008&lt;br /&gt;
&lt;br /&gt;
B.T.T. Yeo, W. Ou, P. Golland. On the Construction of Invertible Filter Banks on the 2-Sphere. Yeo, Ou and Golland. IEEE Transactions on Image Processing. 17(3):283--300. 2008. &lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:Models.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIModeling|Fiber Tract Modeling, Clustering, and Quantitative Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this work is to model the shape of the fiber bundles and use this model description in clustering and statistical analysis of fiber tracts. [[Projects:DTIModeling|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; Mahnaz Maddah, Marek Kubicki, William M. Wells, Carl-Fredrik Westin, Martha E. Shenton and W. Eric L. Grimson, Findings in Schizophrenia by Tract-Oriented DT-MRI Analysis. MICCAI 2008.&lt;br /&gt;
&lt;br /&gt;
M. Maddah, L. Zollei, W. E. L. Grimson, W. M. Wells, Modeling of Anatomical Information in Clustering of White Matter Fiber Trajectories Using Dirichlet Distribution. MMBIA 2008.&lt;br /&gt;
&lt;br /&gt;
M. Maddah, L. Zollei, W. E. L. Grimson, C-F Westin, W. M. Wells, A Mathematical Framework for Incorporating Anatomical Knowledge in DT-MRI Analysis. ISBI 2008.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:TGIt.gif| 150px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:LatentAtlasSegmentation|Joint Segmentation of Image Ensembles via Latent Atlases]] ==&lt;br /&gt;
&lt;br /&gt;
Spatial priors, such as probabilistic atlases, play an important role in MRI segmentation. The atlases are typically generated by averaging manual labels of aligned brain regions across different subjects. However, the availability of comprehensive, reliable and suitable manual segmentations is limited. We therefore propose a joint segmentation of corresponding, aligned structures in the entire population that does not require a probability atlas. [[Projects:LatentAtlasSegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; Joint Segmentation of Image Ensembles via Latent Atlases T. Riklin Raviv, K. Van Leemput, W.M. Wells III and P. Golland, Proceedings of the International Conference on Medical Image Computing and Computer Assisted Intervention (MICCAI), 2009&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:Progress_Registration_Segmentation_Shape.jpg|180px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeBasedSegmentationAndRegistration|Shape Based Segmentation and Registration]] ==&lt;br /&gt;
&lt;br /&gt;
This type of algorithm assigns a tissue type to each voxel in the volume. Incorporating prior shape information biases the label assignment towards contiguous regions that are consistent with the shape model. [[Projects:ShapeBasedSegmentationAndRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:GroupwiseSummary.PNG|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:GroupwiseRegistration|Groupwise Registration]] ==&lt;br /&gt;
&lt;br /&gt;
We extend a previously demonstrated entropy based groupwise registration method to include a free-form deformation model based on B-splines. We provide an efficient implementation using stochastic gradient descents in a multi-resolution setting. We demonstrate the method in application to a set of 50 MRI brain scans and compare the results to a pairwise approach using segmentation labels to evaluate the quality of alignment.&lt;br /&gt;
[[Projects:GroupwiseRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:MIT_DTI_JointSegReg_atlas3D.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIFiberRegistration|Joint Registration and Segmentation of DWI Fiber Tractography]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this work is to jointly register and cluster DWI fiber tracts obtained from a group of subjects. [[Projects:DTIFiberRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:brain.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIClustering|DTI Fiber Clustering and Fiber-Based Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this project is to provide structural description of the white matter architecture as a partition into coherent fiber bundles and clusters, and to use these bundles for quantitative measurement. [[Projects:DTIClustering|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:FMRIEvaluationchart.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:fMRIDetection|fMRI Detection and Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
We are exploring algorithms for improved fMRI detection and interpretation by incorporting spatial priors and anatomical information to guide the detection. [[Projects:fMRIDetection|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:Thalamus_algo_outline.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTISegmentation|DTI-based Segmentation]] ==&lt;br /&gt;
&lt;br /&gt;
Unlike conventional MRI, DTI provides adequate contrast to segment the thalamic nuclei, which are gray matter structures. [[Projects:DTISegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:ConnectivityMap.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIStochasticTractography|Stochastic Tractography]] ==&lt;br /&gt;
&lt;br /&gt;
This work calculates posterior distributions of white matter fiber tract parameters given diffusion observations in a DWI volume.  [[Projects:DTIStochasticTractography|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:HippocampalShapeDifferences.gif|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeAnalysis|Population Analysis of Anatomical Variability]] ==&lt;br /&gt;
&lt;br /&gt;
Our goal is to develop mathematical approaches to modeling anatomical variability within and across populations using tools like local shape descriptors of specific regions of interest and global constellation descriptors of multiple ROI's. [[Projects:ShapeAnalysis|More...]]&lt;br /&gt;
&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=File:Segmentation_example2.png&amp;diff=42429</id>
		<title>File:Segmentation example2.png</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=File:Segmentation_example2.png&amp;diff=42429"/>
		<updated>2009-09-10T18:29:13Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: Example segmentation of brain MRI obtained via SNIP -- lo-res&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Example segmentation of brain MRI obtained via SNIP -- lo-res&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=File:Segmentation_example.png&amp;diff=42424</id>
		<title>File:Segmentation example.png</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=File:Segmentation_example.png&amp;diff=42424"/>
		<updated>2009-09-10T18:23:58Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: Example Segmentation of Brain MRI obtained using SNIP&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Example Segmentation of Brain MRI obtained using SNIP&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Algorithm:MIT&amp;diff=42419</id>
		<title>Algorithm:MIT</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Algorithm:MIT&amp;diff=42419"/>
		<updated>2009-09-10T18:22:32Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; Back to [[Algorithm:Main|NA-MIC Algorithms]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
= Overview of MIT Algorithms (PI: Polina Golland) =&lt;br /&gt;
&lt;br /&gt;
Our group seeks to model statistical variability of anatomy and function across subjects and between populations and to utilize computational models of such variability to improve predictions for individual subjects, as well as characterize populations. Our long-term goal is to develop methods for joint modeling of anatomy and function and to apply them in clinical and scientific studies. We work primarily with anatomical, DTI and fMRI images. We actively contribute implementations of our algorithms to the NAMIC-kit.&lt;br /&gt;
&lt;br /&gt;
= MIT Projects =&lt;br /&gt;
&lt;br /&gt;
== [[Projects:NonparametricSegmentation| Nonparametric Models for Supervised Image Segmentation]] ==&lt;br /&gt;
We propose a non-parametric, probabilistic model for the automatic segmentation of medical images,&lt;br /&gt;
given a training set of images and corresponding label maps. The resulting inference algorithms we&lt;br /&gt;
develop rely on pairwise registrations between the test image and individual training images. The&lt;br /&gt;
training labels are then transferred to the test image and fused to compute a final segmentation of&lt;br /&gt;
the test subject. [[Projects:NonparametricSegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{| cellpadding=&amp;quot;10&amp;quot; style=&amp;quot;text-align:left;&amp;quot;&lt;br /&gt;
| style=&amp;quot;width:15%&amp;quot; | [[Image:MITHippocampalSubfieldSegmentation.png|250px]]&lt;br /&gt;
| style=&amp;quot;width:85%&amp;quot; |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:BayesianMRSegmentation| Bayesian Segmentation of MRI Images]] ==&lt;br /&gt;
&lt;br /&gt;
In this project we develop and validate a method for fully automated segmentation of the subfields of the hippocampus in ultra-high resolution in vivo MRI. [[Projects:HippocampalSubfieldSegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; Automated Segmentation of Hippocampal Subﬁelds from Ultra-High Resolution In Vivo MRI, K. Van Leemput, A. Bakkour, T. Benner, G. Wiggins, L.L. Wald, J. Augustinack, B.C. Dickerson, P. Golland, and B. Fischl. Hippocampus. Accepted for Publication, 2009.&lt;br /&gt;
&lt;br /&gt;
Encoding Probabilistic Atlases Using Bayesian Inference, K. Van Leemput. IEEE Transactions on Medical Imaging. Accepted for Publication, 2009.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:ICluster_templates.gif|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:MultimodalAtlas|Multimodal Atlas]] ==&lt;br /&gt;
&lt;br /&gt;
In this work, we propose and investigate an algorithm that jointly co-registers a collection of images while computing multiple templates. The algorithm, called '''iCluster''', is used to compute multiple atlases for a given population.&lt;br /&gt;
[[Projects:MultimodalAtlas|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; Image-driven Population Analysis through Mixture-Modeling, M.R. Sabuncu, S.K. Balci, M.E. Shenton and P. Golland. IEEE Transactions on Medical Imaging. Accepted for Publication, 2009.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:CoordinateChart.png|250px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:SphericalDemons|Spherical Demons: Fast Surface Registration]] ==&lt;br /&gt;
&lt;br /&gt;
We present the fast Spherical Demons algorithm for registering two spherical images. By exploiting spherical vector spline interpolation theory, we show that a large class of regularizers for the modified demons objective function can be efficiently approximated on the sphere using convolution. Based on the one parameter subgroups of diffeomorphisms, [[Projects:SphericalDemons|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; B.T.T. Yeo, M. Sabuncu, T. Vercauteren, N. Ayache, B. Fischl, P. Golland. Spherical Demons: Fast Surface Registration. MICCAI, volume 5241 of LNCS, 745--753, 2008.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:JointRegSeg.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:RegistrationRegularization|Optimal Atlas Regularization in Image Segmentation]] ==&lt;br /&gt;
&lt;br /&gt;
We propose a unified framework for computing atlases from manually labeled data sets at various degrees of “sharpness” and the joint registration and segmentation of a new brain with these atlases. Using this framework, we investigate the tradeoff between warp regularization and image ﬁdelity, i.e. the smoothness of the new subject warp and the sharpness of the atlas in a segmentation application.&lt;br /&gt;
[[Projects:RegistrationRegularization|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; B.T.T. Yeo, M.R. Sabuncu, R. Desikan, B. Fischl, P. Golland. Effects of Registration Regularization and Atlas Sharpness on Segmentation Accuracy. Medical Image Analysis, 12(5):603--615, 2008. &lt;br /&gt;
  &lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:epi_correction_small.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:FieldmapFreeDistortionCorrection|Fieldmap-Free EPI Distortion Correction]] ==&lt;br /&gt;
&lt;br /&gt;
In this project we aim to improve the EPI distortion correction algorithms [[Projects:FieldmapFreeDistortionCorrection|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt;  Poynton C., Jenkinson M., Whalen S., Golby A.J., Wells III W. Fieldmap-Free Retrospective Registration and Distortion Correction for EPI-Based Functiona Imaging. MICCAI 2008.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:mit_fmri_clustering_parcellation2_xsub.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:fMRIClustering|fMRI clustering]] ==&lt;br /&gt;
&lt;br /&gt;
In this project we study the application of model-based clustering algorithms in identification of functional connectivity in the brain. [[Projects:fMRIClustering|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; D. Lashkari, E. Vul, N. Kanwisher, P. Golland. Discovering Structure in the Space of Activation&lt;br /&gt;
Profiles in fMRI. MICCAI 2008. &lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; A. Venkataraman, K.R.A. Van Dijk, R.L. Buckner, P. Golland. Exploring Functional Connectivity in fMRI via Clustering. ICASSP 2009. &lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:FoldingSpeedDetection.png|150px|]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeAnalysisWithOvercompleteWavelets|Shape Analysis With Overcomplete Wavelets]] ==&lt;br /&gt;
&lt;br /&gt;
In this work, we extend the Euclidean wavelets to the sphere. The resulting over-complete spherical wavelets are invariant to the rotation of the spherical image parameterization. We apply the over-complete spherical wavelet to cortical folding development [[Projects:ShapeAnalysisWithOvercompleteWavelets|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; B.T.T. Yeo, P. Yu, P.E. Grant, B. Fischl, P. Golland. Shape Analysis with Overcomplete Spherical Wavelets. Proceedings of the International Conference on Medical Image Computing and Computer Assisted Intervention (MICCAI), volume 5241 of LNCS, 468--476, 2008&lt;br /&gt;
&lt;br /&gt;
B.T.T. Yeo, W. Ou, P. Golland. On the Construction of Invertible Filter Banks on the 2-Sphere. Yeo, Ou and Golland. IEEE Transactions on Image Processing. 17(3):283--300. 2008. &lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:Models.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIModeling|Fiber Tract Modeling, Clustering, and Quantitative Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this work is to model the shape of the fiber bundles and use this model description in clustering and statistical analysis of fiber tracts. [[Projects:DTIModeling|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; Mahnaz Maddah, Marek Kubicki, William M. Wells, Carl-Fredrik Westin, Martha E. Shenton and W. Eric L. Grimson, Findings in Schizophrenia by Tract-Oriented DT-MRI Analysis. MICCAI 2008.&lt;br /&gt;
&lt;br /&gt;
M. Maddah, L. Zollei, W. E. L. Grimson, W. M. Wells, Modeling of Anatomical Information in Clustering of White Matter Fiber Trajectories Using Dirichlet Distribution. MMBIA 2008.&lt;br /&gt;
&lt;br /&gt;
M. Maddah, L. Zollei, W. E. L. Grimson, C-F Westin, W. M. Wells, A Mathematical Framework for Incorporating Anatomical Knowledge in DT-MRI Analysis. ISBI 2008.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:TGIt.gif| 150px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:LatentAtlasSegmentation|Joint Segmentation of Image Ensembles via Latent Atlases]] ==&lt;br /&gt;
&lt;br /&gt;
Spatial priors, such as probabilistic atlases, play an important role in MRI segmentation. The atlases are typically generated by averaging manual labels of aligned brain regions across different subjects. However, the availability of comprehensive, reliable and suitable manual segmentations is limited. We therefore propose a joint segmentation of corresponding, aligned structures in the entire population that does not require a probability atlas. [[Projects:LatentAtlasSegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:Progress_Registration_Segmentation_Shape.jpg|180px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeBasedSegmentationAndRegistration|Shape Based Segmentation and Registration]] ==&lt;br /&gt;
&lt;br /&gt;
This type of algorithm assigns a tissue type to each voxel in the volume. Incorporating prior shape information biases the label assignment towards contiguous regions that are consistent with the shape model. [[Projects:ShapeBasedSegmentationAndRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:GroupwiseSummary.PNG|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:GroupwiseRegistration|Groupwise Registration]] ==&lt;br /&gt;
&lt;br /&gt;
We extend a previously demonstrated entropy based groupwise registration method to include a free-form deformation model based on B-splines. We provide an efficient implementation using stochastic gradient descents in a multi-resolution setting. We demonstrate the method in application to a set of 50 MRI brain scans and compare the results to a pairwise approach using segmentation labels to evaluate the quality of alignment.&lt;br /&gt;
[[Projects:GroupwiseRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:MIT_DTI_JointSegReg_atlas3D.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIFiberRegistration|Joint Registration and Segmentation of DWI Fiber Tractography]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this work is to jointly register and cluster DWI fiber tracts obtained from a group of subjects. [[Projects:DTIFiberRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:brain.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIClustering|DTI Fiber Clustering and Fiber-Based Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this project is to provide structural description of the white matter architecture as a partition into coherent fiber bundles and clusters, and to use these bundles for quantitative measurement. [[Projects:DTIClustering|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:FMRIEvaluationchart.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:fMRIDetection|fMRI Detection and Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
We are exploring algorithms for improved fMRI detection and interpretation by incorporting spatial priors and anatomical information to guide the detection. [[Projects:fMRIDetection|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:Thalamus_algo_outline.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTISegmentation|DTI-based Segmentation]] ==&lt;br /&gt;
&lt;br /&gt;
Unlike conventional MRI, DTI provides adequate contrast to segment the thalamic nuclei, which are gray matter structures. [[Projects:DTISegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:ConnectivityMap.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIStochasticTractography|Stochastic Tractography]] ==&lt;br /&gt;
&lt;br /&gt;
This work calculates posterior distributions of white matter fiber tract parameters given diffusion observations in a DWI volume.  [[Projects:DTIStochasticTractography|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:HippocampalShapeDifferences.gif|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeAnalysis|Population Analysis of Anatomical Variability]] ==&lt;br /&gt;
&lt;br /&gt;
Our goal is to develop mathematical approaches to modeling anatomical variability within and across populations using tools like local shape descriptors of specific regions of interest and global constellation descriptors of multiple ROI's. [[Projects:ShapeAnalysis|More...]]&lt;br /&gt;
&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Algorithm:MIT&amp;diff=42418</id>
		<title>Algorithm:MIT</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Algorithm:MIT&amp;diff=42418"/>
		<updated>2009-09-10T18:21:55Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: /*  Nonparametric Models for Supervised Image Segmentation */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; Back to [[Algorithm:Main|NA-MIC Algorithms]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
= Overview of MIT Algorithms (PI: Polina Golland) =&lt;br /&gt;
&lt;br /&gt;
Our group seeks to model statistical variability of anatomy and function across subjects and between populations and to utilize computational models of such variability to improve predictions for individual subjects, as well as characterize populations. Our long-term goal is to develop methods for joint modeling of anatomy and function and to apply them in clinical and scientific studies. We work primarily with anatomical, DTI and fMRI images. We actively contribute implementations of our algorithms to the NAMIC-kit.&lt;br /&gt;
&lt;br /&gt;
= MIT Projects =&lt;br /&gt;
&lt;br /&gt;
== [[Projects:NonparametricSegmentation| Nonparametric Models for Supervised Image Segmentation]] ==&lt;br /&gt;
We propose a non-parametric, probabilistic model for the automatic segmentation of medical images,&lt;br /&gt;
given a training set of images and corresponding label maps. The resulting inference algorithms we&lt;br /&gt;
develop rely on pairwise registrations between the test image and individual training images. The&lt;br /&gt;
training labels are then transferred to the test image and fused to compute a final segmentation of&lt;br /&gt;
the test subject. [[Projects:NonparametricSegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{| cellpadding=&amp;quot;10&amp;quot; style=&amp;quot;text-align:left;&amp;quot;&lt;br /&gt;
| style=&amp;quot;width:15%&amp;quot; | [[Image:MITHippocampalSubfieldSegmentation.png|250px]]&lt;br /&gt;
| style=&amp;quot;width:85%&amp;quot; |&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
== [[Projects:BayesianMRSegmentation| Bayesian Segmentation of MRI Images]] ==&lt;br /&gt;
&lt;br /&gt;
In this project we develop and validate a method for fully automated segmentation of the subfields of the hippocampus in ultra-high resolution in vivo MRI. [[Projects:HippocampalSubfieldSegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; Automated Segmentation of Hippocampal Subﬁelds from Ultra-High Resolution In Vivo MRI, K. Van Leemput, A. Bakkour, T. Benner, G. Wiggins, L.L. Wald, J. Augustinack, B.C. Dickerson, P. Golland, and B. Fischl. Hippocampus. Accepted for Publication, 2009.&lt;br /&gt;
&lt;br /&gt;
Encoding Probabilistic Atlases Using Bayesian Inference, K. Van Leemput. IEEE Transactions on Medical Imaging. Accepted for Publication, 2009.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:ICluster_templates.gif|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:MultimodalAtlas|Multimodal Atlas]] ==&lt;br /&gt;
&lt;br /&gt;
In this work, we propose and investigate an algorithm that jointly co-registers a collection of images while computing multiple templates. The algorithm, called '''iCluster''', is used to compute multiple atlases for a given population.&lt;br /&gt;
[[Projects:MultimodalAtlas|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; Image-driven Population Analysis through Mixture-Modeling, M.R. Sabuncu, S.K. Balci, M.E. Shenton and P. Golland. IEEE Transactions on Medical Imaging. Accepted for Publication, 2009.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:CoordinateChart.png|250px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:SphericalDemons|Spherical Demons: Fast Surface Registration]] ==&lt;br /&gt;
&lt;br /&gt;
We present the fast Spherical Demons algorithm for registering two spherical images. By exploiting spherical vector spline interpolation theory, we show that a large class of regularizers for the modified demons objective function can be efficiently approximated on the sphere using convolution. Based on the one parameter subgroups of diffeomorphisms, [[Projects:SphericalDemons|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; B.T.T. Yeo, M. Sabuncu, T. Vercauteren, N. Ayache, B. Fischl, P. Golland. Spherical Demons: Fast Surface Registration. MICCAI, volume 5241 of LNCS, 745--753, 2008.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:JointRegSeg.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:RegistrationRegularization|Optimal Atlas Regularization in Image Segmentation]] ==&lt;br /&gt;
&lt;br /&gt;
We propose a unified framework for computing atlases from manually labeled data sets at various degrees of “sharpness” and the joint registration and segmentation of a new brain with these atlases. Using this framework, we investigate the tradeoff between warp regularization and image ﬁdelity, i.e. the smoothness of the new subject warp and the sharpness of the atlas in a segmentation application.&lt;br /&gt;
[[Projects:RegistrationRegularization|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; B.T.T. Yeo, M.R. Sabuncu, R. Desikan, B. Fischl, P. Golland. Effects of Registration Regularization and Atlas Sharpness on Segmentation Accuracy. Medical Image Analysis, 12(5):603--615, 2008. &lt;br /&gt;
  &lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:epi_correction_small.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:FieldmapFreeDistortionCorrection|Fieldmap-Free EPI Distortion Correction]] ==&lt;br /&gt;
&lt;br /&gt;
In this project we aim to improve the EPI distortion correction algorithms [[Projects:FieldmapFreeDistortionCorrection|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt;  Poynton C., Jenkinson M., Whalen S., Golby A.J., Wells III W. Fieldmap-Free Retrospective Registration and Distortion Correction for EPI-Based Functiona Imaging. MICCAI 2008.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:mit_fmri_clustering_parcellation2_xsub.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:fMRIClustering|fMRI clustering]] ==&lt;br /&gt;
&lt;br /&gt;
In this project we study the application of model-based clustering algorithms in identification of functional connectivity in the brain. [[Projects:fMRIClustering|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; D. Lashkari, E. Vul, N. Kanwisher, P. Golland. Discovering Structure in the Space of Activation&lt;br /&gt;
Profiles in fMRI. MICCAI 2008. &lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; A. Venkataraman, K.R.A. Van Dijk, R.L. Buckner, P. Golland. Exploring Functional Connectivity in fMRI via Clustering. ICASSP 2009. &lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:FoldingSpeedDetection.png|150px|]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeAnalysisWithOvercompleteWavelets|Shape Analysis With Overcomplete Wavelets]] ==&lt;br /&gt;
&lt;br /&gt;
In this work, we extend the Euclidean wavelets to the sphere. The resulting over-complete spherical wavelets are invariant to the rotation of the spherical image parameterization. We apply the over-complete spherical wavelet to cortical folding development [[Projects:ShapeAnalysisWithOvercompleteWavelets|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; B.T.T. Yeo, P. Yu, P.E. Grant, B. Fischl, P. Golland. Shape Analysis with Overcomplete Spherical Wavelets. Proceedings of the International Conference on Medical Image Computing and Computer Assisted Intervention (MICCAI), volume 5241 of LNCS, 468--476, 2008&lt;br /&gt;
&lt;br /&gt;
B.T.T. Yeo, W. Ou, P. Golland. On the Construction of Invertible Filter Banks on the 2-Sphere. Yeo, Ou and Golland. IEEE Transactions on Image Processing. 17(3):283--300. 2008. &lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:Models.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIModeling|Fiber Tract Modeling, Clustering, and Quantitative Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this work is to model the shape of the fiber bundles and use this model description in clustering and statistical analysis of fiber tracts. [[Projects:DTIModeling|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; Mahnaz Maddah, Marek Kubicki, William M. Wells, Carl-Fredrik Westin, Martha E. Shenton and W. Eric L. Grimson, Findings in Schizophrenia by Tract-Oriented DT-MRI Analysis. MICCAI 2008.&lt;br /&gt;
&lt;br /&gt;
M. Maddah, L. Zollei, W. E. L. Grimson, W. M. Wells, Modeling of Anatomical Information in Clustering of White Matter Fiber Trajectories Using Dirichlet Distribution. MMBIA 2008.&lt;br /&gt;
&lt;br /&gt;
M. Maddah, L. Zollei, W. E. L. Grimson, C-F Westin, W. M. Wells, A Mathematical Framework for Incorporating Anatomical Knowledge in DT-MRI Analysis. ISBI 2008.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:TGIt.gif| 150px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:LatentAtlasSegmentation|Joint Segmentation of Image Ensembles via Latent Atlases]] ==&lt;br /&gt;
&lt;br /&gt;
Spatial priors, such as probabilistic atlases, play an important role in MRI segmentation. The atlases are typically generated by averaging manual labels of aligned brain regions across different subjects. However, the availability of comprehensive, reliable and suitable manual segmentations is limited. We therefore propose a joint segmentation of corresponding, aligned structures in the entire population that does not require a probability atlas. [[Projects:LatentAtlasSegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:Progress_Registration_Segmentation_Shape.jpg|180px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeBasedSegmentationAndRegistration|Shape Based Segmentation and Registration]] ==&lt;br /&gt;
&lt;br /&gt;
This type of algorithm assigns a tissue type to each voxel in the volume. Incorporating prior shape information biases the label assignment towards contiguous regions that are consistent with the shape model. [[Projects:ShapeBasedSegmentationAndRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:GroupwiseSummary.PNG|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:GroupwiseRegistration|Groupwise Registration]] ==&lt;br /&gt;
&lt;br /&gt;
We extend a previously demonstrated entropy based groupwise registration method to include a free-form deformation model based on B-splines. We provide an efficient implementation using stochastic gradient descents in a multi-resolution setting. We demonstrate the method in application to a set of 50 MRI brain scans and compare the results to a pairwise approach using segmentation labels to evaluate the quality of alignment.&lt;br /&gt;
[[Projects:GroupwiseRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:MIT_DTI_JointSegReg_atlas3D.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIFiberRegistration|Joint Registration and Segmentation of DWI Fiber Tractography]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this work is to jointly register and cluster DWI fiber tracts obtained from a group of subjects. [[Projects:DTIFiberRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:brain.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIClustering|DTI Fiber Clustering and Fiber-Based Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this project is to provide structural description of the white matter architecture as a partition into coherent fiber bundles and clusters, and to use these bundles for quantitative measurement. [[Projects:DTIClustering|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:FMRIEvaluationchart.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:fMRIDetection|fMRI Detection and Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
We are exploring algorithms for improved fMRI detection and interpretation by incorporting spatial priors and anatomical information to guide the detection. [[Projects:fMRIDetection|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:Thalamus_algo_outline.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTISegmentation|DTI-based Segmentation]] ==&lt;br /&gt;
&lt;br /&gt;
Unlike conventional MRI, DTI provides adequate contrast to segment the thalamic nuclei, which are gray matter structures. [[Projects:DTISegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:ConnectivityMap.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIStochasticTractography|Stochastic Tractography]] ==&lt;br /&gt;
&lt;br /&gt;
This work calculates posterior distributions of white matter fiber tract parameters given diffusion observations in a DWI volume.  [[Projects:DTIStochasticTractography|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:HippocampalShapeDifferences.gif|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeAnalysis|Population Analysis of Anatomical Variability]] ==&lt;br /&gt;
&lt;br /&gt;
Our goal is to develop mathematical approaches to modeling anatomical variability within and across populations using tools like local shape descriptors of specific regions of interest and global constellation descriptors of multiple ROI's. [[Projects:ShapeAnalysis|More...]]&lt;br /&gt;
&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Algorithm:MIT&amp;diff=42417</id>
		<title>Algorithm:MIT</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Algorithm:MIT&amp;diff=42417"/>
		<updated>2009-09-10T18:21:08Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; Back to [[Algorithm:Main|NA-MIC Algorithms]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
= Overview of MIT Algorithms (PI: Polina Golland) =&lt;br /&gt;
&lt;br /&gt;
Our group seeks to model statistical variability of anatomy and function across subjects and between populations and to utilize computational models of such variability to improve predictions for individual subjects, as well as characterize populations. Our long-term goal is to develop methods for joint modeling of anatomy and function and to apply them in clinical and scientific studies. We work primarily with anatomical, DTI and fMRI images. We actively contribute implementations of our algorithms to the NAMIC-kit.&lt;br /&gt;
&lt;br /&gt;
= MIT Projects =&lt;br /&gt;
&lt;br /&gt;
== [[Projects:NonparametricSegmentation| Nonparametric Models for Supervised Image Segmentation]] ==&lt;br /&gt;
We propose a non-parametric, probabilistic model for the automatic segmentation of medical images,&lt;br /&gt;
given a training set of images and corresponding label maps. The resulting inference algorithms we&lt;br /&gt;
develop rely on pairwise registrations between the test image and individual training images. The&lt;br /&gt;
training labels are then transferred to the test image and fused to compute a final segmentation of&lt;br /&gt;
the test subject. [[Projects:NonparametricSegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{| cellpadding=&amp;quot;10&amp;quot; style=&amp;quot;text-align:left;&amp;quot;&lt;br /&gt;
| style=&amp;quot;width:15%&amp;quot; | [[Image:MITHippocampalSubfieldSegmentation.png|250px]]&lt;br /&gt;
| style=&amp;quot;width:85%&amp;quot; |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:BayesianMRSegmentation| Bayesian Segmentation of MRI Images]] ==&lt;br /&gt;
&lt;br /&gt;
In this project we develop and validate a method for fully automated segmentation of the subfields of the hippocampus in ultra-high resolution in vivo MRI. [[Projects:HippocampalSubfieldSegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; Automated Segmentation of Hippocampal Subﬁelds from Ultra-High Resolution In Vivo MRI, K. Van Leemput, A. Bakkour, T. Benner, G. Wiggins, L.L. Wald, J. Augustinack, B.C. Dickerson, P. Golland, and B. Fischl. Hippocampus. Accepted for Publication, 2009.&lt;br /&gt;
&lt;br /&gt;
Encoding Probabilistic Atlases Using Bayesian Inference, K. Van Leemput. IEEE Transactions on Medical Imaging. Accepted for Publication, 2009.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:ICluster_templates.gif|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:MultimodalAtlas|Multimodal Atlas]] ==&lt;br /&gt;
&lt;br /&gt;
In this work, we propose and investigate an algorithm that jointly co-registers a collection of images while computing multiple templates. The algorithm, called '''iCluster''', is used to compute multiple atlases for a given population.&lt;br /&gt;
[[Projects:MultimodalAtlas|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; Image-driven Population Analysis through Mixture-Modeling, M.R. Sabuncu, S.K. Balci, M.E. Shenton and P. Golland. IEEE Transactions on Medical Imaging. Accepted for Publication, 2009.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:CoordinateChart.png|250px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:SphericalDemons|Spherical Demons: Fast Surface Registration]] ==&lt;br /&gt;
&lt;br /&gt;
We present the fast Spherical Demons algorithm for registering two spherical images. By exploiting spherical vector spline interpolation theory, we show that a large class of regularizers for the modified demons objective function can be efficiently approximated on the sphere using convolution. Based on the one parameter subgroups of diffeomorphisms, [[Projects:SphericalDemons|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; B.T.T. Yeo, M. Sabuncu, T. Vercauteren, N. Ayache, B. Fischl, P. Golland. Spherical Demons: Fast Surface Registration. MICCAI, volume 5241 of LNCS, 745--753, 2008.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:JointRegSeg.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:RegistrationRegularization|Optimal Atlas Regularization in Image Segmentation]] ==&lt;br /&gt;
&lt;br /&gt;
We propose a unified framework for computing atlases from manually labeled data sets at various degrees of “sharpness” and the joint registration and segmentation of a new brain with these atlases. Using this framework, we investigate the tradeoff between warp regularization and image ﬁdelity, i.e. the smoothness of the new subject warp and the sharpness of the atlas in a segmentation application.&lt;br /&gt;
[[Projects:RegistrationRegularization|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; B.T.T. Yeo, M.R. Sabuncu, R. Desikan, B. Fischl, P. Golland. Effects of Registration Regularization and Atlas Sharpness on Segmentation Accuracy. Medical Image Analysis, 12(5):603--615, 2008. &lt;br /&gt;
  &lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:epi_correction_small.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:FieldmapFreeDistortionCorrection|Fieldmap-Free EPI Distortion Correction]] ==&lt;br /&gt;
&lt;br /&gt;
In this project we aim to improve the EPI distortion correction algorithms [[Projects:FieldmapFreeDistortionCorrection|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt;  Poynton C., Jenkinson M., Whalen S., Golby A.J., Wells III W. Fieldmap-Free Retrospective Registration and Distortion Correction for EPI-Based Functiona Imaging. MICCAI 2008.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:mit_fmri_clustering_parcellation2_xsub.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:fMRIClustering|fMRI clustering]] ==&lt;br /&gt;
&lt;br /&gt;
In this project we study the application of model-based clustering algorithms in identification of functional connectivity in the brain. [[Projects:fMRIClustering|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; D. Lashkari, E. Vul, N. Kanwisher, P. Golland. Discovering Structure in the Space of Activation&lt;br /&gt;
Profiles in fMRI. MICCAI 2008. &lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; A. Venkataraman, K.R.A. Van Dijk, R.L. Buckner, P. Golland. Exploring Functional Connectivity in fMRI via Clustering. ICASSP 2009. &lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:FoldingSpeedDetection.png|150px|]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeAnalysisWithOvercompleteWavelets|Shape Analysis With Overcomplete Wavelets]] ==&lt;br /&gt;
&lt;br /&gt;
In this work, we extend the Euclidean wavelets to the sphere. The resulting over-complete spherical wavelets are invariant to the rotation of the spherical image parameterization. We apply the over-complete spherical wavelet to cortical folding development [[Projects:ShapeAnalysisWithOvercompleteWavelets|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; B.T.T. Yeo, P. Yu, P.E. Grant, B. Fischl, P. Golland. Shape Analysis with Overcomplete Spherical Wavelets. Proceedings of the International Conference on Medical Image Computing and Computer Assisted Intervention (MICCAI), volume 5241 of LNCS, 468--476, 2008&lt;br /&gt;
&lt;br /&gt;
B.T.T. Yeo, W. Ou, P. Golland. On the Construction of Invertible Filter Banks on the 2-Sphere. Yeo, Ou and Golland. IEEE Transactions on Image Processing. 17(3):283--300. 2008. &lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:Models.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIModeling|Fiber Tract Modeling, Clustering, and Quantitative Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this work is to model the shape of the fiber bundles and use this model description in clustering and statistical analysis of fiber tracts. [[Projects:DTIModeling|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; Mahnaz Maddah, Marek Kubicki, William M. Wells, Carl-Fredrik Westin, Martha E. Shenton and W. Eric L. Grimson, Findings in Schizophrenia by Tract-Oriented DT-MRI Analysis. MICCAI 2008.&lt;br /&gt;
&lt;br /&gt;
M. Maddah, L. Zollei, W. E. L. Grimson, W. M. Wells, Modeling of Anatomical Information in Clustering of White Matter Fiber Trajectories Using Dirichlet Distribution. MMBIA 2008.&lt;br /&gt;
&lt;br /&gt;
M. Maddah, L. Zollei, W. E. L. Grimson, C-F Westin, W. M. Wells, A Mathematical Framework for Incorporating Anatomical Knowledge in DT-MRI Analysis. ISBI 2008.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:TGIt.gif| 150px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:LatentAtlasSegmentation|Joint Segmentation of Image Ensembles via Latent Atlases]] ==&lt;br /&gt;
&lt;br /&gt;
Spatial priors, such as probabilistic atlases, play an important role in MRI segmentation. The atlases are typically generated by averaging manual labels of aligned brain regions across different subjects. However, the availability of comprehensive, reliable and suitable manual segmentations is limited. We therefore propose a joint segmentation of corresponding, aligned structures in the entire population that does not require a probability atlas. [[Projects:LatentAtlasSegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:Progress_Registration_Segmentation_Shape.jpg|180px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeBasedSegmentationAndRegistration|Shape Based Segmentation and Registration]] ==&lt;br /&gt;
&lt;br /&gt;
This type of algorithm assigns a tissue type to each voxel in the volume. Incorporating prior shape information biases the label assignment towards contiguous regions that are consistent with the shape model. [[Projects:ShapeBasedSegmentationAndRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:GroupwiseSummary.PNG|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:GroupwiseRegistration|Groupwise Registration]] ==&lt;br /&gt;
&lt;br /&gt;
We extend a previously demonstrated entropy based groupwise registration method to include a free-form deformation model based on B-splines. We provide an efficient implementation using stochastic gradient descents in a multi-resolution setting. We demonstrate the method in application to a set of 50 MRI brain scans and compare the results to a pairwise approach using segmentation labels to evaluate the quality of alignment.&lt;br /&gt;
[[Projects:GroupwiseRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:MIT_DTI_JointSegReg_atlas3D.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIFiberRegistration|Joint Registration and Segmentation of DWI Fiber Tractography]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this work is to jointly register and cluster DWI fiber tracts obtained from a group of subjects. [[Projects:DTIFiberRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:brain.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIClustering|DTI Fiber Clustering and Fiber-Based Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this project is to provide structural description of the white matter architecture as a partition into coherent fiber bundles and clusters, and to use these bundles for quantitative measurement. [[Projects:DTIClustering|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:FMRIEvaluationchart.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:fMRIDetection|fMRI Detection and Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
We are exploring algorithms for improved fMRI detection and interpretation by incorporting spatial priors and anatomical information to guide the detection. [[Projects:fMRIDetection|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:Thalamus_algo_outline.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTISegmentation|DTI-based Segmentation]] ==&lt;br /&gt;
&lt;br /&gt;
Unlike conventional MRI, DTI provides adequate contrast to segment the thalamic nuclei, which are gray matter structures. [[Projects:DTISegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:ConnectivityMap.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIStochasticTractography|Stochastic Tractography]] ==&lt;br /&gt;
&lt;br /&gt;
This work calculates posterior distributions of white matter fiber tract parameters given diffusion observations in a DWI volume.  [[Projects:DTIStochasticTractography|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:HippocampalShapeDifferences.gif|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeAnalysis|Population Analysis of Anatomical Variability]] ==&lt;br /&gt;
&lt;br /&gt;
Our goal is to develop mathematical approaches to modeling anatomical variability within and across populations using tools like local shape descriptors of specific regions of interest and global constellation descriptors of multiple ROI's. [[Projects:ShapeAnalysis|More...]]&lt;br /&gt;
&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Algorithm:MIT&amp;diff=42416</id>
		<title>Algorithm:MIT</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Algorithm:MIT&amp;diff=42416"/>
		<updated>2009-09-10T18:20:56Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; Back to [[Algorithm:Main|NA-MIC Algorithms]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
= Overview of MIT Algorithms (PI: Polina Golland) =&lt;br /&gt;
&lt;br /&gt;
Our group seeks to model statistical variability of anatomy and function across subjects and between populations and to utilize computational models of such variability to improve predictions for individual subjects, as well as characterize populations. Our long-term goal is to develop methods for joint modeling of anatomy and function and to apply them in clinical and scientific studies. We work primarily with anatomical, DTI and fMRI images. We actively contribute implementations of our algorithms to the NAMIC-kit.&lt;br /&gt;
&lt;br /&gt;
= MIT Projects =&lt;br /&gt;
&lt;br /&gt;
{| cellpadding=&amp;quot;10&amp;quot; style=&amp;quot;text-align:left;&amp;quot;&lt;br /&gt;
| style=&amp;quot;width:15%&amp;quot; | [[Image:MITHippocampalSubfieldSegmentation.png|250px]]&lt;br /&gt;
| style=&amp;quot;width:85%&amp;quot; |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:NonparametricSegmentation| Nonparametric Models for Supervised Image Segmentation]] ==&lt;br /&gt;
We propose a non-parametric, probabilistic model for the automatic segmentation of medical images,&lt;br /&gt;
given a training set of images and corresponding label maps. The resulting inference algorithms we&lt;br /&gt;
develop rely on pairwise registrations between the test image and individual training images. The&lt;br /&gt;
training labels are then transferred to the test image and fused to compute a final segmentation of&lt;br /&gt;
the test subject. [[Projects:NonparametricSegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{| cellpadding=&amp;quot;10&amp;quot; style=&amp;quot;text-align:left;&amp;quot;&lt;br /&gt;
| style=&amp;quot;width:15%&amp;quot; | [[Image:MITHippocampalSubfieldSegmentation.png|250px]]&lt;br /&gt;
| style=&amp;quot;width:85%&amp;quot; |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:BayesianMRSegmentation| Bayesian Segmentation of MRI Images]] ==&lt;br /&gt;
&lt;br /&gt;
In this project we develop and validate a method for fully automated segmentation of the subfields of the hippocampus in ultra-high resolution in vivo MRI. [[Projects:HippocampalSubfieldSegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; Automated Segmentation of Hippocampal Subﬁelds from Ultra-High Resolution In Vivo MRI, K. Van Leemput, A. Bakkour, T. Benner, G. Wiggins, L.L. Wald, J. Augustinack, B.C. Dickerson, P. Golland, and B. Fischl. Hippocampus. Accepted for Publication, 2009.&lt;br /&gt;
&lt;br /&gt;
Encoding Probabilistic Atlases Using Bayesian Inference, K. Van Leemput. IEEE Transactions on Medical Imaging. Accepted for Publication, 2009.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:ICluster_templates.gif|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:MultimodalAtlas|Multimodal Atlas]] ==&lt;br /&gt;
&lt;br /&gt;
In this work, we propose and investigate an algorithm that jointly co-registers a collection of images while computing multiple templates. The algorithm, called '''iCluster''', is used to compute multiple atlases for a given population.&lt;br /&gt;
[[Projects:MultimodalAtlas|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; Image-driven Population Analysis through Mixture-Modeling, M.R. Sabuncu, S.K. Balci, M.E. Shenton and P. Golland. IEEE Transactions on Medical Imaging. Accepted for Publication, 2009.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:CoordinateChart.png|250px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:SphericalDemons|Spherical Demons: Fast Surface Registration]] ==&lt;br /&gt;
&lt;br /&gt;
We present the fast Spherical Demons algorithm for registering two spherical images. By exploiting spherical vector spline interpolation theory, we show that a large class of regularizers for the modified demons objective function can be efficiently approximated on the sphere using convolution. Based on the one parameter subgroups of diffeomorphisms, [[Projects:SphericalDemons|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; B.T.T. Yeo, M. Sabuncu, T. Vercauteren, N. Ayache, B. Fischl, P. Golland. Spherical Demons: Fast Surface Registration. MICCAI, volume 5241 of LNCS, 745--753, 2008.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:JointRegSeg.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:RegistrationRegularization|Optimal Atlas Regularization in Image Segmentation]] ==&lt;br /&gt;
&lt;br /&gt;
We propose a unified framework for computing atlases from manually labeled data sets at various degrees of “sharpness” and the joint registration and segmentation of a new brain with these atlases. Using this framework, we investigate the tradeoff between warp regularization and image ﬁdelity, i.e. the smoothness of the new subject warp and the sharpness of the atlas in a segmentation application.&lt;br /&gt;
[[Projects:RegistrationRegularization|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; B.T.T. Yeo, M.R. Sabuncu, R. Desikan, B. Fischl, P. Golland. Effects of Registration Regularization and Atlas Sharpness on Segmentation Accuracy. Medical Image Analysis, 12(5):603--615, 2008. &lt;br /&gt;
  &lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:epi_correction_small.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:FieldmapFreeDistortionCorrection|Fieldmap-Free EPI Distortion Correction]] ==&lt;br /&gt;
&lt;br /&gt;
In this project we aim to improve the EPI distortion correction algorithms [[Projects:FieldmapFreeDistortionCorrection|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt;  Poynton C., Jenkinson M., Whalen S., Golby A.J., Wells III W. Fieldmap-Free Retrospective Registration and Distortion Correction for EPI-Based Functiona Imaging. MICCAI 2008.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:mit_fmri_clustering_parcellation2_xsub.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:fMRIClustering|fMRI clustering]] ==&lt;br /&gt;
&lt;br /&gt;
In this project we study the application of model-based clustering algorithms in identification of functional connectivity in the brain. [[Projects:fMRIClustering|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; D. Lashkari, E. Vul, N. Kanwisher, P. Golland. Discovering Structure in the Space of Activation&lt;br /&gt;
Profiles in fMRI. MICCAI 2008. &lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; A. Venkataraman, K.R.A. Van Dijk, R.L. Buckner, P. Golland. Exploring Functional Connectivity in fMRI via Clustering. ICASSP 2009. &lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:FoldingSpeedDetection.png|150px|]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeAnalysisWithOvercompleteWavelets|Shape Analysis With Overcomplete Wavelets]] ==&lt;br /&gt;
&lt;br /&gt;
In this work, we extend the Euclidean wavelets to the sphere. The resulting over-complete spherical wavelets are invariant to the rotation of the spherical image parameterization. We apply the over-complete spherical wavelet to cortical folding development [[Projects:ShapeAnalysisWithOvercompleteWavelets|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; B.T.T. Yeo, P. Yu, P.E. Grant, B. Fischl, P. Golland. Shape Analysis with Overcomplete Spherical Wavelets. Proceedings of the International Conference on Medical Image Computing and Computer Assisted Intervention (MICCAI), volume 5241 of LNCS, 468--476, 2008&lt;br /&gt;
&lt;br /&gt;
B.T.T. Yeo, W. Ou, P. Golland. On the Construction of Invertible Filter Banks on the 2-Sphere. Yeo, Ou and Golland. IEEE Transactions on Image Processing. 17(3):283--300. 2008. &lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:Models.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIModeling|Fiber Tract Modeling, Clustering, and Quantitative Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this work is to model the shape of the fiber bundles and use this model description in clustering and statistical analysis of fiber tracts. [[Projects:DTIModeling|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; Mahnaz Maddah, Marek Kubicki, William M. Wells, Carl-Fredrik Westin, Martha E. Shenton and W. Eric L. Grimson, Findings in Schizophrenia by Tract-Oriented DT-MRI Analysis. MICCAI 2008.&lt;br /&gt;
&lt;br /&gt;
M. Maddah, L. Zollei, W. E. L. Grimson, W. M. Wells, Modeling of Anatomical Information in Clustering of White Matter Fiber Trajectories Using Dirichlet Distribution. MMBIA 2008.&lt;br /&gt;
&lt;br /&gt;
M. Maddah, L. Zollei, W. E. L. Grimson, C-F Westin, W. M. Wells, A Mathematical Framework for Incorporating Anatomical Knowledge in DT-MRI Analysis. ISBI 2008.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:TGIt.gif| 150px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:LatentAtlasSegmentation|Joint Segmentation of Image Ensembles via Latent Atlases]] ==&lt;br /&gt;
&lt;br /&gt;
Spatial priors, such as probabilistic atlases, play an important role in MRI segmentation. The atlases are typically generated by averaging manual labels of aligned brain regions across different subjects. However, the availability of comprehensive, reliable and suitable manual segmentations is limited. We therefore propose a joint segmentation of corresponding, aligned structures in the entire population that does not require a probability atlas. [[Projects:LatentAtlasSegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:Progress_Registration_Segmentation_Shape.jpg|180px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeBasedSegmentationAndRegistration|Shape Based Segmentation and Registration]] ==&lt;br /&gt;
&lt;br /&gt;
This type of algorithm assigns a tissue type to each voxel in the volume. Incorporating prior shape information biases the label assignment towards contiguous regions that are consistent with the shape model. [[Projects:ShapeBasedSegmentationAndRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:GroupwiseSummary.PNG|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:GroupwiseRegistration|Groupwise Registration]] ==&lt;br /&gt;
&lt;br /&gt;
We extend a previously demonstrated entropy based groupwise registration method to include a free-form deformation model based on B-splines. We provide an efficient implementation using stochastic gradient descents in a multi-resolution setting. We demonstrate the method in application to a set of 50 MRI brain scans and compare the results to a pairwise approach using segmentation labels to evaluate the quality of alignment.&lt;br /&gt;
[[Projects:GroupwiseRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:MIT_DTI_JointSegReg_atlas3D.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIFiberRegistration|Joint Registration and Segmentation of DWI Fiber Tractography]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this work is to jointly register and cluster DWI fiber tracts obtained from a group of subjects. [[Projects:DTIFiberRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:brain.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIClustering|DTI Fiber Clustering and Fiber-Based Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this project is to provide structural description of the white matter architecture as a partition into coherent fiber bundles and clusters, and to use these bundles for quantitative measurement. [[Projects:DTIClustering|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:FMRIEvaluationchart.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:fMRIDetection|fMRI Detection and Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
We are exploring algorithms for improved fMRI detection and interpretation by incorporting spatial priors and anatomical information to guide the detection. [[Projects:fMRIDetection|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:Thalamus_algo_outline.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTISegmentation|DTI-based Segmentation]] ==&lt;br /&gt;
&lt;br /&gt;
Unlike conventional MRI, DTI provides adequate contrast to segment the thalamic nuclei, which are gray matter structures. [[Projects:DTISegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:ConnectivityMap.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIStochasticTractography|Stochastic Tractography]] ==&lt;br /&gt;
&lt;br /&gt;
This work calculates posterior distributions of white matter fiber tract parameters given diffusion observations in a DWI volume.  [[Projects:DTIStochasticTractography|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:HippocampalShapeDifferences.gif|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeAnalysis|Population Analysis of Anatomical Variability]] ==&lt;br /&gt;
&lt;br /&gt;
Our goal is to develop mathematical approaches to modeling anatomical variability within and across populations using tools like local shape descriptors of specific regions of interest and global constellation descriptors of multiple ROI's. [[Projects:ShapeAnalysis|More...]]&lt;br /&gt;
&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Algorithm:MIT&amp;diff=42411</id>
		<title>Algorithm:MIT</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Algorithm:MIT&amp;diff=42411"/>
		<updated>2009-09-10T18:12:14Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: /* MIT Projects */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; Back to [[Algorithm:Main|NA-MIC Algorithms]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
= Overview of MIT Algorithms (PI: Polina Golland) =&lt;br /&gt;
&lt;br /&gt;
Our group seeks to model statistical variability of anatomy and function across subjects and between populations and to utilize computational models of such variability to improve predictions for individual subjects, as well as characterize populations. Our long-term goal is to develop methods for joint modeling of anatomy and function and to apply them in clinical and scientific studies. We work primarily with anatomical, DTI and fMRI images. We actively contribute implementations of our algorithms to the NAMIC-kit.&lt;br /&gt;
&lt;br /&gt;
= MIT Projects =&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== [[Projects:NonparametricSegmentation| Nonparametric Models for Supervised Image Segmentation]] ==&lt;br /&gt;
We propose a non-parametric, probabilistic model for the automatic segmentation of medical images,&lt;br /&gt;
given a training set of images and corresponding label maps. The resulting inference algorithms we&lt;br /&gt;
develop rely on pairwise registrations between the test image and individual training images. The&lt;br /&gt;
training labels are then transferred to the test image and fused to compute a final segmentation of&lt;br /&gt;
the test subject. [[Projects:NonparametricSegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{| cellpadding=&amp;quot;10&amp;quot; style=&amp;quot;text-align:left;&amp;quot;&lt;br /&gt;
| style=&amp;quot;width:15%&amp;quot; | [[Image:MITHippocampalSubfieldSegmentation.png|250px]]&lt;br /&gt;
| style=&amp;quot;width:85%&amp;quot; |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:BayesianMRSegmentation| Bayesian Segmentation of MRI Images]] ==&lt;br /&gt;
&lt;br /&gt;
In this project we develop and validate a method for fully automated segmentation of the subfields of the hippocampus in ultra-high resolution in vivo MRI. [[Projects:HippocampalSubfieldSegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; Automated Segmentation of Hippocampal Subﬁelds from Ultra-High Resolution In Vivo MRI, K. Van Leemput, A. Bakkour, T. Benner, G. Wiggins, L.L. Wald, J. Augustinack, B.C. Dickerson, P. Golland, and B. Fischl. Hippocampus. Accepted for Publication, 2009.&lt;br /&gt;
&lt;br /&gt;
Encoding Probabilistic Atlases Using Bayesian Inference, K. Van Leemput. IEEE Transactions on Medical Imaging. Accepted for Publication, 2009.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:ICluster_templates.gif|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:MultimodalAtlas|Multimodal Atlas]] ==&lt;br /&gt;
&lt;br /&gt;
In this work, we propose and investigate an algorithm that jointly co-registers a collection of images while computing multiple templates. The algorithm, called '''iCluster''', is used to compute multiple atlases for a given population.&lt;br /&gt;
[[Projects:MultimodalAtlas|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; Image-driven Population Analysis through Mixture-Modeling, M.R. Sabuncu, S.K. Balci, M.E. Shenton and P. Golland. IEEE Transactions on Medical Imaging. Accepted for Publication, 2009.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:CoordinateChart.png|250px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:SphericalDemons|Spherical Demons: Fast Surface Registration]] ==&lt;br /&gt;
&lt;br /&gt;
We present the fast Spherical Demons algorithm for registering two spherical images. By exploiting spherical vector spline interpolation theory, we show that a large class of regularizers for the modified demons objective function can be efficiently approximated on the sphere using convolution. Based on the one parameter subgroups of diffeomorphisms, [[Projects:SphericalDemons|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; B.T.T. Yeo, M. Sabuncu, T. Vercauteren, N. Ayache, B. Fischl, P. Golland. Spherical Demons: Fast Surface Registration. MICCAI, volume 5241 of LNCS, 745--753, 2008.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:JointRegSeg.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:RegistrationRegularization|Optimal Atlas Regularization in Image Segmentation]] ==&lt;br /&gt;
&lt;br /&gt;
We propose a unified framework for computing atlases from manually labeled data sets at various degrees of “sharpness” and the joint registration and segmentation of a new brain with these atlases. Using this framework, we investigate the tradeoff between warp regularization and image ﬁdelity, i.e. the smoothness of the new subject warp and the sharpness of the atlas in a segmentation application.&lt;br /&gt;
[[Projects:RegistrationRegularization|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; B.T.T. Yeo, M.R. Sabuncu, R. Desikan, B. Fischl, P. Golland. Effects of Registration Regularization and Atlas Sharpness on Segmentation Accuracy. Medical Image Analysis, 12(5):603--615, 2008. &lt;br /&gt;
  &lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:epi_correction_small.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:FieldmapFreeDistortionCorrection|Fieldmap-Free EPI Distortion Correction]] ==&lt;br /&gt;
&lt;br /&gt;
In this project we aim to improve the EPI distortion correction algorithms [[Projects:FieldmapFreeDistortionCorrection|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt;  Poynton C., Jenkinson M., Whalen S., Golby A.J., Wells III W. Fieldmap-Free Retrospective Registration and Distortion Correction for EPI-Based Functiona Imaging. MICCAI 2008.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:mit_fmri_clustering_parcellation2_xsub.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:fMRIClustering|fMRI clustering]] ==&lt;br /&gt;
&lt;br /&gt;
In this project we study the application of model-based clustering algorithms in identification of functional connectivity in the brain. [[Projects:fMRIClustering|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; D. Lashkari, E. Vul, N. Kanwisher, P. Golland. Discovering Structure in the Space of Activation&lt;br /&gt;
Profiles in fMRI. MICCAI 2008. &lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:FoldingSpeedDetection.png|150px|]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeAnalysisWithOvercompleteWavelets|Shape Analysis With Overcomplete Wavelets]] ==&lt;br /&gt;
&lt;br /&gt;
In this work, we extend the Euclidean wavelets to the sphere. The resulting over-complete spherical wavelets are invariant to the rotation of the spherical image parameterization. We apply the over-complete spherical wavelet to cortical folding development [[Projects:ShapeAnalysisWithOvercompleteWavelets|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; B.T.T. Yeo, P. Yu, P.E. Grant, B. Fischl, P. Golland. Shape Analysis with Overcomplete Spherical Wavelets. Proceedings of the International Conference on Medical Image Computing and Computer Assisted Intervention (MICCAI), volume 5241 of LNCS, 468--476, 2008&lt;br /&gt;
&lt;br /&gt;
B.T.T. Yeo, W. Ou, P. Golland. On the Construction of Invertible Filter Banks on the 2-Sphere. Yeo, Ou and Golland. IEEE Transactions on Image Processing. 17(3):283--300. 2008. &lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:Models.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIModeling|Fiber Tract Modeling, Clustering, and Quantitative Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this work is to model the shape of the fiber bundles and use this model description in clustering and statistical analysis of fiber tracts. [[Projects:DTIModeling|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; Mahnaz Maddah, Marek Kubicki, William M. Wells, Carl-Fredrik Westin, Martha E. Shenton and W. Eric L. Grimson, Findings in Schizophrenia by Tract-Oriented DT-MRI Analysis. MICCAI 2008.&lt;br /&gt;
&lt;br /&gt;
M. Maddah, L. Zollei, W. E. L. Grimson, W. M. Wells, Modeling of Anatomical Information in Clustering of White Matter Fiber Trajectories Using Dirichlet Distribution. MMBIA 2008.&lt;br /&gt;
&lt;br /&gt;
M. Maddah, L. Zollei, W. E. L. Grimson, C-F Westin, W. M. Wells, A Mathematical Framework for Incorporating Anatomical Knowledge in DT-MRI Analysis. ISBI 2008.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:TGIt.gif| 150px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:LatentAtlasSegmentation|Joint Segmentation of Image Ensembles via Latent Atlases]] ==&lt;br /&gt;
&lt;br /&gt;
Spatial priors, such as probabilistic atlases, play an important role in MRI segmentation. The atlases are typically generated by averaging manual labels of aligned brain regions across different subjects. However, the availability of comprehensive, reliable and suitable manual segmentations is limited. We therefore propose a joint segmentation of corresponding, aligned structures in the entire population that does not require a probability atlas. [[Projects:LatentAtlasSegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:Progress_Registration_Segmentation_Shape.jpg|180px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeBasedSegmentationAndRegistration|Shape Based Segmentation and Registration]] ==&lt;br /&gt;
&lt;br /&gt;
This type of algorithm assigns a tissue type to each voxel in the volume. Incorporating prior shape information biases the label assignment towards contiguous regions that are consistent with the shape model. [[Projects:ShapeBasedSegmentationAndRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:GroupwiseSummary.PNG|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:GroupwiseRegistration|Groupwise Registration]] ==&lt;br /&gt;
&lt;br /&gt;
We extend a previously demonstrated entropy based groupwise registration method to include a free-form deformation model based on B-splines. We provide an efficient implementation using stochastic gradient descents in a multi-resolution setting. We demonstrate the method in application to a set of 50 MRI brain scans and compare the results to a pairwise approach using segmentation labels to evaluate the quality of alignment.&lt;br /&gt;
[[Projects:GroupwiseRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:MIT_DTI_JointSegReg_atlas3D.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIFiberRegistration|Joint Registration and Segmentation of DWI Fiber Tractography]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this work is to jointly register and cluster DWI fiber tracts obtained from a group of subjects. [[Projects:DTIFiberRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:brain.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIClustering|DTI Fiber Clustering and Fiber-Based Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this project is to provide structural description of the white matter architecture as a partition into coherent fiber bundles and clusters, and to use these bundles for quantitative measurement. [[Projects:DTIClustering|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:FMRIEvaluationchart.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:fMRIDetection|fMRI Detection and Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
We are exploring algorithms for improved fMRI detection and interpretation by incorporting spatial priors and anatomical information to guide the detection. [[Projects:fMRIDetection|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:Thalamus_algo_outline.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTISegmentation|DTI-based Segmentation]] ==&lt;br /&gt;
&lt;br /&gt;
Unlike conventional MRI, DTI provides adequate contrast to segment the thalamic nuclei, which are gray matter structures. [[Projects:DTISegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:ConnectivityMap.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIStochasticTractography|Stochastic Tractography]] ==&lt;br /&gt;
&lt;br /&gt;
This work calculates posterior distributions of white matter fiber tract parameters given diffusion observations in a DWI volume.  [[Projects:DTIStochasticTractography|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:HippocampalShapeDifferences.gif|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeAnalysis|Population Analysis of Anatomical Variability]] ==&lt;br /&gt;
&lt;br /&gt;
Our goal is to develop mathematical approaches to modeling anatomical variability within and across populations using tools like local shape descriptors of specific regions of interest and global constellation descriptors of multiple ROI's. [[Projects:ShapeAnalysis|More...]]&lt;br /&gt;
&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Algorithm:MIT&amp;diff=42410</id>
		<title>Algorithm:MIT</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Algorithm:MIT&amp;diff=42410"/>
		<updated>2009-09-10T18:10:13Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: /* MIT Projects */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; Back to [[Algorithm:Main|NA-MIC Algorithms]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
= Overview of MIT Algorithms (PI: Polina Golland) =&lt;br /&gt;
&lt;br /&gt;
Our group seeks to model statistical variability of anatomy and function across subjects and between populations and to utilize computational models of such variability to improve predictions for individual subjects, as well as characterize populations. Our long-term goal is to develop methods for joint modeling of anatomy and function and to apply them in clinical and scientific studies. We work primarily with anatomical, DTI and fMRI images. We actively contribute implementations of our algorithms to the NAMIC-kit.&lt;br /&gt;
&lt;br /&gt;
= MIT Projects =&lt;br /&gt;
&lt;br /&gt;
{| cellpadding=&amp;quot;10&amp;quot; style=&amp;quot;text-align:left;&amp;quot;&lt;br /&gt;
| style=&amp;quot;width:15%&amp;quot; | [[Image:MITHippocampalSubfieldSegmentation.png|250px]]&lt;br /&gt;
| style=&amp;quot;width:85%&amp;quot; |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:NonparametricSegmentation| Nonparametric Models for Supervised Image Segmentation]] ==&lt;br /&gt;
We propose a non-parametric, probabilistic model for the automatic segmentation of medical images,&lt;br /&gt;
given a training set of images and corresponding label maps. The resulting inference algorithms we&lt;br /&gt;
develop rely on pairwise registrations between the test image and individual training images. The&lt;br /&gt;
training labels are then transferred to the test image and fused to compute a final segmentation of&lt;br /&gt;
the test subject. == [[Projects:NonparametricSegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
== [[Projects:BayesianMRSegmentation| Bayesian Segmentation of MRI Images]] ==&lt;br /&gt;
&lt;br /&gt;
In this project we develop and validate a method for fully automated segmentation of the subfields of the hippocampus in ultra-high resolution in vivo MRI. [[Projects:HippocampalSubfieldSegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; Automated Segmentation of Hippocampal Subﬁelds from Ultra-High Resolution In Vivo MRI, K. Van Leemput, A. Bakkour, T. Benner, G. Wiggins, L.L. Wald, J. Augustinack, B.C. Dickerson, P. Golland, and B. Fischl. Hippocampus. Accepted for Publication, 2009.&lt;br /&gt;
&lt;br /&gt;
Encoding Probabilistic Atlases Using Bayesian Inference, K. Van Leemput. IEEE Transactions on Medical Imaging. Accepted for Publication, 2009.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:ICluster_templates.gif|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:MultimodalAtlas|Multimodal Atlas]] ==&lt;br /&gt;
&lt;br /&gt;
In this work, we propose and investigate an algorithm that jointly co-registers a collection of images while computing multiple templates. The algorithm, called '''iCluster''', is used to compute multiple atlases for a given population.&lt;br /&gt;
[[Projects:MultimodalAtlas|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; Image-driven Population Analysis through Mixture-Modeling, M.R. Sabuncu, S.K. Balci, M.E. Shenton and P. Golland. IEEE Transactions on Medical Imaging. Accepted for Publication, 2009.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:CoordinateChart.png|250px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:SphericalDemons|Spherical Demons: Fast Surface Registration]] ==&lt;br /&gt;
&lt;br /&gt;
We present the fast Spherical Demons algorithm for registering two spherical images. By exploiting spherical vector spline interpolation theory, we show that a large class of regularizers for the modified demons objective function can be efficiently approximated on the sphere using convolution. Based on the one parameter subgroups of diffeomorphisms, [[Projects:SphericalDemons|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; B.T.T. Yeo, M. Sabuncu, T. Vercauteren, N. Ayache, B. Fischl, P. Golland. Spherical Demons: Fast Surface Registration. MICCAI, volume 5241 of LNCS, 745--753, 2008.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:JointRegSeg.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:RegistrationRegularization|Optimal Atlas Regularization in Image Segmentation]] ==&lt;br /&gt;
&lt;br /&gt;
We propose a unified framework for computing atlases from manually labeled data sets at various degrees of “sharpness” and the joint registration and segmentation of a new brain with these atlases. Using this framework, we investigate the tradeoff between warp regularization and image ﬁdelity, i.e. the smoothness of the new subject warp and the sharpness of the atlas in a segmentation application.&lt;br /&gt;
[[Projects:RegistrationRegularization|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; B.T.T. Yeo, M.R. Sabuncu, R. Desikan, B. Fischl, P. Golland. Effects of Registration Regularization and Atlas Sharpness on Segmentation Accuracy. Medical Image Analysis, 12(5):603--615, 2008. &lt;br /&gt;
  &lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:epi_correction_small.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:FieldmapFreeDistortionCorrection|Fieldmap-Free EPI Distortion Correction]] ==&lt;br /&gt;
&lt;br /&gt;
In this project we aim to improve the EPI distortion correction algorithms [[Projects:FieldmapFreeDistortionCorrection|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt;  Poynton C., Jenkinson M., Whalen S., Golby A.J., Wells III W. Fieldmap-Free Retrospective Registration and Distortion Correction for EPI-Based Functiona Imaging. MICCAI 2008.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:mit_fmri_clustering_parcellation2_xsub.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:fMRIClustering|fMRI clustering]] ==&lt;br /&gt;
&lt;br /&gt;
In this project we study the application of model-based clustering algorithms in identification of functional connectivity in the brain. [[Projects:fMRIClustering|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; D. Lashkari, E. Vul, N. Kanwisher, P. Golland. Discovering Structure in the Space of Activation&lt;br /&gt;
Profiles in fMRI. MICCAI 2008. &lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:FoldingSpeedDetection.png|150px|]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeAnalysisWithOvercompleteWavelets|Shape Analysis With Overcomplete Wavelets]] ==&lt;br /&gt;
&lt;br /&gt;
In this work, we extend the Euclidean wavelets to the sphere. The resulting over-complete spherical wavelets are invariant to the rotation of the spherical image parameterization. We apply the over-complete spherical wavelet to cortical folding development [[Projects:ShapeAnalysisWithOvercompleteWavelets|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; B.T.T. Yeo, P. Yu, P.E. Grant, B. Fischl, P. Golland. Shape Analysis with Overcomplete Spherical Wavelets. Proceedings of the International Conference on Medical Image Computing and Computer Assisted Intervention (MICCAI), volume 5241 of LNCS, 468--476, 2008&lt;br /&gt;
&lt;br /&gt;
B.T.T. Yeo, W. Ou, P. Golland. On the Construction of Invertible Filter Banks on the 2-Sphere. Yeo, Ou and Golland. IEEE Transactions on Image Processing. 17(3):283--300. 2008. &lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:Models.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIModeling|Fiber Tract Modeling, Clustering, and Quantitative Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this work is to model the shape of the fiber bundles and use this model description in clustering and statistical analysis of fiber tracts. [[Projects:DTIModeling|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; Mahnaz Maddah, Marek Kubicki, William M. Wells, Carl-Fredrik Westin, Martha E. Shenton and W. Eric L. Grimson, Findings in Schizophrenia by Tract-Oriented DT-MRI Analysis. MICCAI 2008.&lt;br /&gt;
&lt;br /&gt;
M. Maddah, L. Zollei, W. E. L. Grimson, W. M. Wells, Modeling of Anatomical Information in Clustering of White Matter Fiber Trajectories Using Dirichlet Distribution. MMBIA 2008.&lt;br /&gt;
&lt;br /&gt;
M. Maddah, L. Zollei, W. E. L. Grimson, C-F Westin, W. M. Wells, A Mathematical Framework for Incorporating Anatomical Knowledge in DT-MRI Analysis. ISBI 2008.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:TGIt.gif| 150px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:LatentAtlasSegmentation|Joint Segmentation of Image Ensembles via Latent Atlases]] ==&lt;br /&gt;
&lt;br /&gt;
Spatial priors, such as probabilistic atlases, play an important role in MRI segmentation. The atlases are typically generated by averaging manual labels of aligned brain regions across different subjects. However, the availability of comprehensive, reliable and suitable manual segmentations is limited. We therefore propose a joint segmentation of corresponding, aligned structures in the entire population that does not require a probability atlas. [[Projects:LatentAtlasSegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:Progress_Registration_Segmentation_Shape.jpg|180px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeBasedSegmentationAndRegistration|Shape Based Segmentation and Registration]] ==&lt;br /&gt;
&lt;br /&gt;
This type of algorithm assigns a tissue type to each voxel in the volume. Incorporating prior shape information biases the label assignment towards contiguous regions that are consistent with the shape model. [[Projects:ShapeBasedSegmentationAndRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:GroupwiseSummary.PNG|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:GroupwiseRegistration|Groupwise Registration]] ==&lt;br /&gt;
&lt;br /&gt;
We extend a previously demonstrated entropy based groupwise registration method to include a free-form deformation model based on B-splines. We provide an efficient implementation using stochastic gradient descents in a multi-resolution setting. We demonstrate the method in application to a set of 50 MRI brain scans and compare the results to a pairwise approach using segmentation labels to evaluate the quality of alignment.&lt;br /&gt;
[[Projects:GroupwiseRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:MIT_DTI_JointSegReg_atlas3D.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIFiberRegistration|Joint Registration and Segmentation of DWI Fiber Tractography]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this work is to jointly register and cluster DWI fiber tracts obtained from a group of subjects. [[Projects:DTIFiberRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:brain.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIClustering|DTI Fiber Clustering and Fiber-Based Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this project is to provide structural description of the white matter architecture as a partition into coherent fiber bundles and clusters, and to use these bundles for quantitative measurement. [[Projects:DTIClustering|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:FMRIEvaluationchart.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:fMRIDetection|fMRI Detection and Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
We are exploring algorithms for improved fMRI detection and interpretation by incorporting spatial priors and anatomical information to guide the detection. [[Projects:fMRIDetection|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:Thalamus_algo_outline.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTISegmentation|DTI-based Segmentation]] ==&lt;br /&gt;
&lt;br /&gt;
Unlike conventional MRI, DTI provides adequate contrast to segment the thalamic nuclei, which are gray matter structures. [[Projects:DTISegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:ConnectivityMap.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIStochasticTractography|Stochastic Tractography]] ==&lt;br /&gt;
&lt;br /&gt;
This work calculates posterior distributions of white matter fiber tract parameters given diffusion observations in a DWI volume.  [[Projects:DTIStochasticTractography|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:HippocampalShapeDifferences.gif|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeAnalysis|Population Analysis of Anatomical Variability]] ==&lt;br /&gt;
&lt;br /&gt;
Our goal is to develop mathematical approaches to modeling anatomical variability within and across populations using tools like local shape descriptors of specific regions of interest and global constellation descriptors of multiple ROI's. [[Projects:ShapeAnalysis|More...]]&lt;br /&gt;
&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:MultimodalAtlas&amp;diff=36528</id>
		<title>Projects:MultimodalAtlas</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:MultimodalAtlas&amp;diff=36528"/>
		<updated>2009-04-23T17:45:04Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: /* Publications */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Back to [[NA-MIC_Internal_Collaborations:StructuralImageAnalysis|NA-MIC Collaborations]], [[Algorithm:MIT|MIT Algorithms]], [[DBP2:Harvard|Harvard DBP2]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
Today, computational anatomy studies are mainly hypothesis-driven, aiming to identify and characterize structural or functional differences between, for instance a group of patients with a specific disorder and control subjects. This type of approach has two premises: clinical classification of the subjects and spatial correspondence across the images. In practice, achieving either can be challenging. First, the complex spectrum of symptoms of neuro-degenerative disorders like schizophrenia and overlapping symptoms across different types of dementia like Alzheimer's disease, delirium and depression make a diagnosis based on standardized clinical tests like the mental status examination difficult. Second, across-subject correspondence in the images is a particularly hard problem that requires different approaches in various contexts. A popular technique is to normalize all subjects into a standard space, such as the Talairach space, by registering each image with a single, universal template image that represents an average brain. However, the quality of such an approach is limited by the accuracy with which the universal template represents the population in the study.&lt;br /&gt;
&lt;br /&gt;
With the increasing availability of medical images, data-driven algorithms offer the ability to probe a population and potentially discover sub-groups that may differ in unexpected ways. In this paper, we propose and demonstrate an efficient probabilistic clustering algorithm, called '''iCluster''', that:&lt;br /&gt;
&lt;br /&gt;
* computes a small number of templates that summarize a given population of images,&lt;br /&gt;
* simultaneously co-registers all the images using a nonlinear transformation model,&lt;br /&gt;
* assigns each input image to a template.&lt;br /&gt;
&lt;br /&gt;
The templates are guaranteed to live in an affine-normalized space, i.e., they are spatially aligned with respect to an affine transformation model.&lt;br /&gt;
&lt;br /&gt;
= Description =&lt;br /&gt;
&lt;br /&gt;
[[Image:GenerativeModel.png|center|400px|Generative Model used in iCluster.]]&lt;br /&gt;
&lt;br /&gt;
'''iCluster''' is derived from a simple generative model. We assume that there are a fixed and known number of template images. Then the process that generates an observed image is as follows: a template is randomly drawn – note that the probability that governs this process doesn’t have to be uniform. Next, the chosen template is warped with a random transformation and i.i.d Gaussian noise is added to this warped image to generate an observed image. This process is repeated multiple times to generate a collection of images.&lt;br /&gt;
&lt;br /&gt;
We formulate the problem as a maximum likelihood solution. We employ a Generalized Maximum Likelihood (GEM) algorithm to solve the problem. The GEM algorithm is derived using Jensen's inequality and has three steps: &lt;br /&gt;
*E-step: Given the estimates for the template images, template prior probabilities and noise variance image estimates from the previous iteration, the algorithm updates the memberships of each image as the posterior probability of an image being generated from a particular template.&lt;br /&gt;
*T-step: Given the membership estimates from the previous E-step, the algorithm updates the template image, template prior and noise variance estimates using closed-form expressions.&lt;br /&gt;
*R-step: Given the membership, template, template prior and noise variance estimates from the pervious iterations, the algorithm updates the warps for each image. This step is a collection of pairwise registration instances, where each image is aligned with an effective template image. The effective template image is a weighted average of the current individual templates, where the weights are current memberships.&lt;br /&gt;
&lt;br /&gt;
The resulting algorithm is fast and efficient: each iteration's time and memory requirements are linear in the number of voxels, input images and templates.&lt;br /&gt;
We employ a stochastic subsampling strategy in each one of the E, T and R steps. A random subsample of voxels (typically less than 1% of the total voxels) are used for the computations. &lt;br /&gt;
In the R-step, we employ a B-spline nonlinear transformation model and the optimization is done using gradient-descent. During this optimization, the gradients are normalized so that each cluster (i.e. the images assigned to the same template image) are subject to an average of zero deformation. This is an extension of the &amp;quot;anchoring&amp;quot; strategy used in groupwise registration algorithms. This is usually done by subtracting the average gradient from the individual gradients.&lt;br /&gt;
&lt;br /&gt;
= Results =&lt;br /&gt;
&lt;br /&gt;
We present two experiments. The first one demonstrates the use of iCluster for building a multi-template atlas in a segmentation application. In the second experiment, we employ iCluster to compute multiple templates of a large data set that contains 416 brain MRI. Our results show that these templates correspond to different age groups.  We find the correlation between the image-based clustering, and demographic and clinical characteristics particularly intriguing, given the fact that iCluster did not employ the latter information.&lt;br /&gt;
&lt;br /&gt;
'''Experiment 1: Segmentation Label Alignment'''&lt;br /&gt;
&lt;br /&gt;
In this experiment, we used a data set of 50 whole brain MR brain images (of size 256x256x124 and voxel dimensions 0.9375x0.9375x1.5 mm) that&lt;br /&gt;
contained 16 patients with first episode schizophrenia (SZ), 17 patients with first-episode affective disorder (AFF) and 17 healthy subjects (CON). First episode patients are relatively free of chronicity-related confounds such as the long-term effects of medication, thus any structural differences between the three groups are subtle, local and difficult to identify in individual scans.&lt;br /&gt;
&lt;br /&gt;
The 50 MR images also contained manual labels of certain medial temporal lobe structures: the superior temporal gyrus (STG), hippocampus (HIPP), amygdala (AMY) and parahippocampal gyrus (PHG). We used these manual labels to explore label alignment across subjects under different groupings: on the whole data set, on random partitionings of the data set into two subsets of equal size, on the clinical grouping, and on the image-based clustering as determined by iCluster.&lt;br /&gt;
&lt;br /&gt;
[[Image:Two_templates_shenton50.png|center|600px|Two templates in a 50 subject MRI.]]&lt;br /&gt;
&lt;br /&gt;
We spatially normalized all the subjects into \textit{a standard space} using the iCluster algorithm with one-template and a 32x32x32 B-spline transformation model, and explored the alignment of the manual labels for clinical and image-based groupings. For each region of interest, such as amygdala, we computed the modified Haussdorff distance (MHD) in the standard space. MHD is a non -symmetric distance measure between the boundaries of two labels and is zero for perfect alignment.The MHD values for each region of interest were then summed up to obtain a total label distance for each ordered subject pair.&lt;br /&gt;
The following figure shows the total label distance for all subject pairings under the different groupings. We note that image-based clustering of iCluster (both with two-template and three-template)&lt;br /&gt;
groups subjects that have better label alignment, whereas the clinical grouping demonstrates no such coherence.&lt;br /&gt;
&lt;br /&gt;
[[Image:LabelAlignmentMatrixShenton50.png|center|600px|Label Alignment Matrices for the three groupings in the Shenton50 data set.]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
'''Experiment 2: Age groups in the OASIS data set'''&lt;br /&gt;
&lt;br /&gt;
In this experiment, we used the OASIS data set [http://www.oasis-brains.org] which consists of 416 pre-processed (skull stripped and gain-field corrected) brain MR images of subjects aged 18-96 years including individuals with early-stage Alzheimer's disease (AD). We ran iCluster on the whole data set while varying the number of templates from 2 through 6. Each run took approximately 4-8&lt;br /&gt;
hours on a 16 processor PC with 128GB RAM. For two- and three templates the algorithm computed unique and structurally different templates. We observed that these templates were robust: they were the same for random subsets of the data set of as little as 60 subjects. For larger number of templates, however, we observed that the computed templates were not all unique, or corresponded to single outlier subjects, or were not robust to random sub-sampling of the data set.&lt;br /&gt;
&lt;br /&gt;
The following figure shows the three robust templates computed by iCluster.&lt;br /&gt;
&lt;br /&gt;
[[Image:Three_templates_oasis.png|center|600px|Three templates of the OASIS data.]]&lt;br /&gt;
&lt;br /&gt;
The following figure shows the difference images between the three templates shown above.&lt;br /&gt;
&lt;br /&gt;
Difference_templates_oasis.png&lt;br /&gt;
&lt;br /&gt;
[[Image:Difference_templates_oasis.png|center|600px|Difference between the three templates of the OASIS data]]&lt;br /&gt;
 &lt;br /&gt;
The following figure includes the age distributions estimated using Parzen windowing with a Gaussian kernel and a s.t.d. of 4 years for each cluster identified by the algorithm.&lt;br /&gt;
&lt;br /&gt;
[[Image:Age_distributions_oasis.png|center|600px|Age groups in the OASIS data]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
'''Software'''&lt;br /&gt;
&lt;br /&gt;
The algorithm is currently implemented in the Insight ToolKit (ITK) and will be made publicly available. We also plan to integrate it into Slicer.&lt;br /&gt;
&lt;br /&gt;
= Key Investigators =&lt;br /&gt;
&lt;br /&gt;
MIT Algorithms: Mert R. Sabuncu, Serdar K. Balci and Polina Golland&lt;br /&gt;
&lt;br /&gt;
Harvard DBP 2: M.E. Shenton, M. Kubicki and S. Bouix&lt;br /&gt;
&lt;br /&gt;
= Publications =&lt;br /&gt;
&lt;br /&gt;
* &amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''NEW: '''&amp;lt;/font&amp;gt; Image-driven Population Analysis through Mixture-Modeling, M.R. Sabuncu, S.K. Balci, M.E. Shenton and P. Golland. IEEE Transactions on Medical Imaging. Accepted for Publication, 2009.&lt;br /&gt;
&lt;br /&gt;
* [http://www.na-mic.org/publications/pages/display?search=Projects%3AMultimodalAtlas&amp;amp;submit=Search&amp;amp;words=all&amp;amp;title=checked&amp;amp;keywords=checked&amp;amp;authors=checked&amp;amp;abstract=checked&amp;amp;sponsors=checked&amp;amp;searchbytag=checked| NA-MIC Publications Database]&lt;br /&gt;
&lt;br /&gt;
[[Category: Registration]]&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Algorithm:MIT&amp;diff=36526</id>
		<title>Algorithm:MIT</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Algorithm:MIT&amp;diff=36526"/>
		<updated>2009-04-23T17:44:32Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: /* Multimodal Atlas */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Back to [[Algorithm:Main|NA-MIC Algorithms]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
= Overview of MIT Algorithms (PI: Polina Golland) =&lt;br /&gt;
&lt;br /&gt;
Our group seeks to model statistical variability of anatomy and function across subjects and between populations and to utilize computational models of such variability to improve predictions for individual subjects, as well as characterize populations. Our long-term goal is to develop methods for joint modeling of anatomy and function and to apply them in clinical and scientific studies. We work primarily with anatomical, DTI and fMRI images. We actively contribute implementations of our algorithms to the NAMIC-kit.&lt;br /&gt;
&lt;br /&gt;
= MIT Projects =&lt;br /&gt;
&lt;br /&gt;
{| cellpadding=&amp;quot;10&amp;quot;&lt;br /&gt;
| style=&amp;quot;width:15%&amp;quot; | [[Image:CoordinateChart.png|200px]]&lt;br /&gt;
| style=&amp;quot;width:85%&amp;quot; | &lt;br /&gt;
&lt;br /&gt;
== [[Projects:SphericalDemons|Spherical Demons: Fast Surface Registration]] ==&lt;br /&gt;
&lt;br /&gt;
We present the fast Spherical Demons algorithm for registering two spherical images. By exploiting spherical vector spline interpolation theory, we show that a large class of regularizers for the modified demons objective function can be efficiently approximated on the sphere using convolution. Based on the one parameter subgroups of diffeomorphisms, [[Projects:SphericalDemons|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; B.T.T. Yeo, M. Sabuncu, T. Vercauteren, N. Ayache, B. Fischl, P. Golland. Spherical Demons: Fast Surface Registration. MICCAI, volume 5241 of LNCS, 745--753, 2008&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:Progress_Registration_Segmentation_Shape.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeBasedSegmentationAndRegistration|Shape Based Segmentation and Registration]] ==&lt;br /&gt;
&lt;br /&gt;
This type of algorithm assigns a tissue type to each voxel in the volume. Incorporating prior shape information biases the label assignment towards contiguous regions that are consistent with the shape model. [[Projects:ShapeBasedSegmentationAndRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:JointRegSeg.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:RegistrationRegularization|Optimal Atlas Regularization in Image Segmentation]] ==&lt;br /&gt;
&lt;br /&gt;
We propose a unified framework for computing atlases from manually labeled data sets at various degrees of “sharpness” and the joint registration and segmentation of a new brain with these atlases. Using this framework, we investigate the tradeoff between warp regularization and image ﬁdelity, i.e. the smoothness of the new subject warp and the sharpness of the atlas in a segmentation application.&lt;br /&gt;
[[Projects:RegistrationRegularization|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; B.T.T. Yeo, M.R. Sabuncu, R. Desikan, B. Fischl, P. Golland. Effects of Registration Regularization and Atlas Sharpness on Segmentation Accuracy. Medical Image Analysis, 12(5):603--615, 2008. &lt;br /&gt;
  &lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:ICluster_templates.gif|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:MultimodalAtlas|Multimodal Atlas]] ==&lt;br /&gt;
&lt;br /&gt;
In this work, we propose and investigate an algorithm that jointly co-registers a collection of images while computing multiple templates. The algorithm, called '''iCluster''', is used to compute multiple atlases for a given population.&lt;br /&gt;
[[Projects:MultimodalAtlas|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; Image-driven Population Analysis through Mixture-Modeling, M.R. Sabuncu, S.K. Balci, M.E. Shenton and P. Golland. IEEE Transactions on Medical Imaging. Accepted for Publication, 2009.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:GroupwiseSummary.PNG|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:GroupwiseRegistration|Groupwise Registration]] ==&lt;br /&gt;
&lt;br /&gt;
We extend a previously demonstrated entropy based groupwise registration method to include a free-form deformation model based on B-splines. We provide an efficient implementation using stochastic gradient descents in a multi-resolution setting. We demonstrate the method in application to a set of 50 MRI brain scans and compare the results to a pairwise approach using segmentation labels to evaluate the quality of alignment.&lt;br /&gt;
[[Projects:GroupwiseRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:FoldingSpeedDetection.png|200px|]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeAnalysisWithOvercompleteWavelets|Shape Analysis With Overcomplete Wavelets]] ==&lt;br /&gt;
&lt;br /&gt;
In this work, we extend the Euclidean wavelets to the sphere. The resulting over-complete spherical wavelets are invariant to the rotation of the spherical image parameterization. We apply the over-complete spherical wavelet to cortical folding development [[Projects:ShapeAnalysisWithOvercompleteWavelets|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; B.T.T. Yeo, P. Yu, P.E. Grant, B. Fischl, P. Golland. Shape Analysis with Overcomplete Spherical Wavelets. Proceedings of the International Conference on Medical Image Computing and Computer Assisted Intervention (MICCAI), volume 5241 of LNCS, 468--476, 2008&lt;br /&gt;
&lt;br /&gt;
B.T.T. Yeo, W. Ou, P. Golland. On the Construction of Invertible Filter Banks on the 2-Sphere. Yeo, Ou and Golland. IEEE Transactions on Image Processing. 17(3):283--300. 2008. &lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:MITHippocampalSubfieldSegmentation.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:HippocampalSubfieldSegmentation|Model-Based Segmentation of Hippocampal Subﬁelds in In Vivo MRI]] ==&lt;br /&gt;
&lt;br /&gt;
In this project we develop and validate a method for fully automated segmentation of the subfields of the hippocampus in ultra-high resolution in vivo MRI. [[Projects:HippocampalSubfieldSegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; K. Van Leemput, A. Bakkour, T. Benner, G. Wiggins, L.L. Wald, J. Augustinack, B.C. Dickerson, P. Golland, B. Fischl. Model-Based Segmentation of Hippocampal Subfields in Ultra-High Resolution In Vivo MRI.  MICCAI 2008. &lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| | [[Image:mit_fmri_clustering_parcellation2_xsub.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:fMRIClustering|fMRI clustering]] ==&lt;br /&gt;
&lt;br /&gt;
In this project we study the application of model-based clustering algorithms in identification of functional connectivity in the brain. [[Projects:fMRIClustering|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; D. Lashkari, E. Vul, N. Kanwisher, P. Golland. Discovering Structure in the Space of Activation&lt;br /&gt;
Profiles in fMRI. MICCAI 2008. &lt;br /&gt;
  &lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:MIT_DTI_JointSegReg_atlas3D.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIFiberRegistration|Joint Registration and Segmentation of DWI Fiber Tractography]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this work is to jointly register and cluster DWI fiber tracts obtained from a group of subjects. [[Projects:DTIFiberRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:brain.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIClustering|DTI Fiber Clustering and Fiber-Based Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this project is to provide structural description of the white matter architecture as a partition into coherent fiber bundles and clusters, and to use these bundles for quantitative measurement. [[Projects:DTIClustering|More...]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:Models.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIModeling|Fiber Tract Modeling, Clustering, and Quantitative Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this work is to model the shape of the fiber bundles and use this model description in clustering and statistical analysis of fiber tracts. [[Projects:DTIModeling|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; &lt;br /&gt;
&lt;br /&gt;
Mahnaz Maddah, Marek Kubicki, William M. Wells, Carl-Fredrik Westin, Martha E. Shenton and W. Eric L. Grimson, Findings in Schizophrenia by Tract-Oriented DT-MRI Analysis. MICCAI 2008.&lt;br /&gt;
&lt;br /&gt;
M. Maddah, L. Zollei, W. E. L. Grimson, W. M. Wells, Modeling of Anatomical Information in Clustering of White Matter Fiber Trajectories Using Dirichlet Distribution. MMBIA 2008.&lt;br /&gt;
&lt;br /&gt;
M. Maddah, L. Zollei, W. E. L. Grimson, C-F Westin, W. M. Wells, A Mathematical Framework for Incorporating Anatomical Knowledge in DT-MRI Analysis. ISBI 2008.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:FMRIEvaluationchart.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:fMRIDetection|fMRI Detection and Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
We are exploring algorithms for improved fMRI detection and interpretation by incorporting spatial priors and anatomical information to guide the detection. [[Projects:fMRIDetection|More...]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:Thalamus_algo_outline.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTISegmentation|DTI-based Segmentation]] ==&lt;br /&gt;
&lt;br /&gt;
Unlike conventional MRI, DTI provides adequate contrast to segment the thalamic nuclei, which are gray matter structures. [[Projects:DTISegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:ConnectivityMap.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIStochasticTractography|Stochastic Tractography]] ==&lt;br /&gt;
&lt;br /&gt;
This work calculates posterior distributions of white matter fiber tract parameters given diffusion observations in a DWI volume.  [[Projects:DTIStochasticTractography|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:HippocampalShapeDifferences.gif|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeAnalysis|Population Analysis of Anatomical Variability]] ==&lt;br /&gt;
&lt;br /&gt;
Our goal is to develop mathematical approaches to modeling anatomical variability within and across populations using tools like local shape descriptors of specific regions of interest and global constellation descriptors of multiple ROI's. [[Projects:ShapeAnalysis|More...]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Algorithm:MIT&amp;diff=36524</id>
		<title>Algorithm:MIT</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Algorithm:MIT&amp;diff=36524"/>
		<updated>2009-04-23T17:44:21Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: /* Multimodal Atlas */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Back to [[Algorithm:Main|NA-MIC Algorithms]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
= Overview of MIT Algorithms (PI: Polina Golland) =&lt;br /&gt;
&lt;br /&gt;
Our group seeks to model statistical variability of anatomy and function across subjects and between populations and to utilize computational models of such variability to improve predictions for individual subjects, as well as characterize populations. Our long-term goal is to develop methods for joint modeling of anatomy and function and to apply them in clinical and scientific studies. We work primarily with anatomical, DTI and fMRI images. We actively contribute implementations of our algorithms to the NAMIC-kit.&lt;br /&gt;
&lt;br /&gt;
= MIT Projects =&lt;br /&gt;
&lt;br /&gt;
{| cellpadding=&amp;quot;10&amp;quot;&lt;br /&gt;
| style=&amp;quot;width:15%&amp;quot; | [[Image:CoordinateChart.png|200px]]&lt;br /&gt;
| style=&amp;quot;width:85%&amp;quot; | &lt;br /&gt;
&lt;br /&gt;
== [[Projects:SphericalDemons|Spherical Demons: Fast Surface Registration]] ==&lt;br /&gt;
&lt;br /&gt;
We present the fast Spherical Demons algorithm for registering two spherical images. By exploiting spherical vector spline interpolation theory, we show that a large class of regularizers for the modified demons objective function can be efficiently approximated on the sphere using convolution. Based on the one parameter subgroups of diffeomorphisms, [[Projects:SphericalDemons|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; B.T.T. Yeo, M. Sabuncu, T. Vercauteren, N. Ayache, B. Fischl, P. Golland. Spherical Demons: Fast Surface Registration. MICCAI, volume 5241 of LNCS, 745--753, 2008&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:Progress_Registration_Segmentation_Shape.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeBasedSegmentationAndRegistration|Shape Based Segmentation and Registration]] ==&lt;br /&gt;
&lt;br /&gt;
This type of algorithm assigns a tissue type to each voxel in the volume. Incorporating prior shape information biases the label assignment towards contiguous regions that are consistent with the shape model. [[Projects:ShapeBasedSegmentationAndRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:JointRegSeg.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:RegistrationRegularization|Optimal Atlas Regularization in Image Segmentation]] ==&lt;br /&gt;
&lt;br /&gt;
We propose a unified framework for computing atlases from manually labeled data sets at various degrees of “sharpness” and the joint registration and segmentation of a new brain with these atlases. Using this framework, we investigate the tradeoff between warp regularization and image ﬁdelity, i.e. the smoothness of the new subject warp and the sharpness of the atlas in a segmentation application.&lt;br /&gt;
[[Projects:RegistrationRegularization|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; B.T.T. Yeo, M.R. Sabuncu, R. Desikan, B. Fischl, P. Golland. Effects of Registration Regularization and Atlas Sharpness on Segmentation Accuracy. Medical Image Analysis, 12(5):603--615, 2008. &lt;br /&gt;
  &lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:ICluster_templates.gif|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:MultimodalAtlas|Multimodal Atlas]] ==&lt;br /&gt;
&lt;br /&gt;
In this work, we propose and investigate an algorithm that jointly co-registers a collection of images while computing multiple templates. The algorithm, called '''iCluster''', is used to compute multiple atlases for a given population.&lt;br /&gt;
[[Projects:MultimodalAtlas|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; mage-driven Population Analysis through Mixture-Modeling, M.R. Sabuncu, S.K. Balci, M.E. Shenton and P. Golland. IEEE Transactions on Medical Imaging. Accepted for Publication, 2009.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:GroupwiseSummary.PNG|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:GroupwiseRegistration|Groupwise Registration]] ==&lt;br /&gt;
&lt;br /&gt;
We extend a previously demonstrated entropy based groupwise registration method to include a free-form deformation model based on B-splines. We provide an efficient implementation using stochastic gradient descents in a multi-resolution setting. We demonstrate the method in application to a set of 50 MRI brain scans and compare the results to a pairwise approach using segmentation labels to evaluate the quality of alignment.&lt;br /&gt;
[[Projects:GroupwiseRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:FoldingSpeedDetection.png|200px|]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeAnalysisWithOvercompleteWavelets|Shape Analysis With Overcomplete Wavelets]] ==&lt;br /&gt;
&lt;br /&gt;
In this work, we extend the Euclidean wavelets to the sphere. The resulting over-complete spherical wavelets are invariant to the rotation of the spherical image parameterization. We apply the over-complete spherical wavelet to cortical folding development [[Projects:ShapeAnalysisWithOvercompleteWavelets|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; B.T.T. Yeo, P. Yu, P.E. Grant, B. Fischl, P. Golland. Shape Analysis with Overcomplete Spherical Wavelets. Proceedings of the International Conference on Medical Image Computing and Computer Assisted Intervention (MICCAI), volume 5241 of LNCS, 468--476, 2008&lt;br /&gt;
&lt;br /&gt;
B.T.T. Yeo, W. Ou, P. Golland. On the Construction of Invertible Filter Banks on the 2-Sphere. Yeo, Ou and Golland. IEEE Transactions on Image Processing. 17(3):283--300. 2008. &lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:MITHippocampalSubfieldSegmentation.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:HippocampalSubfieldSegmentation|Model-Based Segmentation of Hippocampal Subﬁelds in In Vivo MRI]] ==&lt;br /&gt;
&lt;br /&gt;
In this project we develop and validate a method for fully automated segmentation of the subfields of the hippocampus in ultra-high resolution in vivo MRI. [[Projects:HippocampalSubfieldSegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; K. Van Leemput, A. Bakkour, T. Benner, G. Wiggins, L.L. Wald, J. Augustinack, B.C. Dickerson, P. Golland, B. Fischl. Model-Based Segmentation of Hippocampal Subfields in Ultra-High Resolution In Vivo MRI.  MICCAI 2008. &lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| | [[Image:mit_fmri_clustering_parcellation2_xsub.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:fMRIClustering|fMRI clustering]] ==&lt;br /&gt;
&lt;br /&gt;
In this project we study the application of model-based clustering algorithms in identification of functional connectivity in the brain. [[Projects:fMRIClustering|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; D. Lashkari, E. Vul, N. Kanwisher, P. Golland. Discovering Structure in the Space of Activation&lt;br /&gt;
Profiles in fMRI. MICCAI 2008. &lt;br /&gt;
  &lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:MIT_DTI_JointSegReg_atlas3D.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIFiberRegistration|Joint Registration and Segmentation of DWI Fiber Tractography]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this work is to jointly register and cluster DWI fiber tracts obtained from a group of subjects. [[Projects:DTIFiberRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:brain.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIClustering|DTI Fiber Clustering and Fiber-Based Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this project is to provide structural description of the white matter architecture as a partition into coherent fiber bundles and clusters, and to use these bundles for quantitative measurement. [[Projects:DTIClustering|More...]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:Models.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIModeling|Fiber Tract Modeling, Clustering, and Quantitative Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this work is to model the shape of the fiber bundles and use this model description in clustering and statistical analysis of fiber tracts. [[Projects:DTIModeling|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; &lt;br /&gt;
&lt;br /&gt;
Mahnaz Maddah, Marek Kubicki, William M. Wells, Carl-Fredrik Westin, Martha E. Shenton and W. Eric L. Grimson, Findings in Schizophrenia by Tract-Oriented DT-MRI Analysis. MICCAI 2008.&lt;br /&gt;
&lt;br /&gt;
M. Maddah, L. Zollei, W. E. L. Grimson, W. M. Wells, Modeling of Anatomical Information in Clustering of White Matter Fiber Trajectories Using Dirichlet Distribution. MMBIA 2008.&lt;br /&gt;
&lt;br /&gt;
M. Maddah, L. Zollei, W. E. L. Grimson, C-F Westin, W. M. Wells, A Mathematical Framework for Incorporating Anatomical Knowledge in DT-MRI Analysis. ISBI 2008.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:FMRIEvaluationchart.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:fMRIDetection|fMRI Detection and Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
We are exploring algorithms for improved fMRI detection and interpretation by incorporting spatial priors and anatomical information to guide the detection. [[Projects:fMRIDetection|More...]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:Thalamus_algo_outline.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTISegmentation|DTI-based Segmentation]] ==&lt;br /&gt;
&lt;br /&gt;
Unlike conventional MRI, DTI provides adequate contrast to segment the thalamic nuclei, which are gray matter structures. [[Projects:DTISegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:ConnectivityMap.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIStochasticTractography|Stochastic Tractography]] ==&lt;br /&gt;
&lt;br /&gt;
This work calculates posterior distributions of white matter fiber tract parameters given diffusion observations in a DWI volume.  [[Projects:DTIStochasticTractography|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:HippocampalShapeDifferences.gif|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeAnalysis|Population Analysis of Anatomical Variability]] ==&lt;br /&gt;
&lt;br /&gt;
Our goal is to develop mathematical approaches to modeling anatomical variability within and across populations using tools like local shape descriptors of specific regions of interest and global constellation descriptors of multiple ROI's. [[Projects:ShapeAnalysis|More...]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:MultimodalAtlas&amp;diff=36523</id>
		<title>Projects:MultimodalAtlas</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:MultimodalAtlas&amp;diff=36523"/>
		<updated>2009-04-23T17:43:17Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: /* Publications */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Back to [[NA-MIC_Internal_Collaborations:StructuralImageAnalysis|NA-MIC Collaborations]], [[Algorithm:MIT|MIT Algorithms]], [[DBP2:Harvard|Harvard DBP2]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
Today, computational anatomy studies are mainly hypothesis-driven, aiming to identify and characterize structural or functional differences between, for instance a group of patients with a specific disorder and control subjects. This type of approach has two premises: clinical classification of the subjects and spatial correspondence across the images. In practice, achieving either can be challenging. First, the complex spectrum of symptoms of neuro-degenerative disorders like schizophrenia and overlapping symptoms across different types of dementia like Alzheimer's disease, delirium and depression make a diagnosis based on standardized clinical tests like the mental status examination difficult. Second, across-subject correspondence in the images is a particularly hard problem that requires different approaches in various contexts. A popular technique is to normalize all subjects into a standard space, such as the Talairach space, by registering each image with a single, universal template image that represents an average brain. However, the quality of such an approach is limited by the accuracy with which the universal template represents the population in the study.&lt;br /&gt;
&lt;br /&gt;
With the increasing availability of medical images, data-driven algorithms offer the ability to probe a population and potentially discover sub-groups that may differ in unexpected ways. In this paper, we propose and demonstrate an efficient probabilistic clustering algorithm, called '''iCluster''', that:&lt;br /&gt;
&lt;br /&gt;
* computes a small number of templates that summarize a given population of images,&lt;br /&gt;
* simultaneously co-registers all the images using a nonlinear transformation model,&lt;br /&gt;
* assigns each input image to a template.&lt;br /&gt;
&lt;br /&gt;
The templates are guaranteed to live in an affine-normalized space, i.e., they are spatially aligned with respect to an affine transformation model.&lt;br /&gt;
&lt;br /&gt;
= Description =&lt;br /&gt;
&lt;br /&gt;
[[Image:GenerativeModel.png|center|400px|Generative Model used in iCluster.]]&lt;br /&gt;
&lt;br /&gt;
'''iCluster''' is derived from a simple generative model. We assume that there are a fixed and known number of template images. Then the process that generates an observed image is as follows: a template is randomly drawn – note that the probability that governs this process doesn’t have to be uniform. Next, the chosen template is warped with a random transformation and i.i.d Gaussian noise is added to this warped image to generate an observed image. This process is repeated multiple times to generate a collection of images.&lt;br /&gt;
&lt;br /&gt;
We formulate the problem as a maximum likelihood solution. We employ a Generalized Maximum Likelihood (GEM) algorithm to solve the problem. The GEM algorithm is derived using Jensen's inequality and has three steps: &lt;br /&gt;
*E-step: Given the estimates for the template images, template prior probabilities and noise variance image estimates from the previous iteration, the algorithm updates the memberships of each image as the posterior probability of an image being generated from a particular template.&lt;br /&gt;
*T-step: Given the membership estimates from the previous E-step, the algorithm updates the template image, template prior and noise variance estimates using closed-form expressions.&lt;br /&gt;
*R-step: Given the membership, template, template prior and noise variance estimates from the pervious iterations, the algorithm updates the warps for each image. This step is a collection of pairwise registration instances, where each image is aligned with an effective template image. The effective template image is a weighted average of the current individual templates, where the weights are current memberships.&lt;br /&gt;
&lt;br /&gt;
The resulting algorithm is fast and efficient: each iteration's time and memory requirements are linear in the number of voxels, input images and templates.&lt;br /&gt;
We employ a stochastic subsampling strategy in each one of the E, T and R steps. A random subsample of voxels (typically less than 1% of the total voxels) are used for the computations. &lt;br /&gt;
In the R-step, we employ a B-spline nonlinear transformation model and the optimization is done using gradient-descent. During this optimization, the gradients are normalized so that each cluster (i.e. the images assigned to the same template image) are subject to an average of zero deformation. This is an extension of the &amp;quot;anchoring&amp;quot; strategy used in groupwise registration algorithms. This is usually done by subtracting the average gradient from the individual gradients.&lt;br /&gt;
&lt;br /&gt;
= Results =&lt;br /&gt;
&lt;br /&gt;
We present two experiments. The first one demonstrates the use of iCluster for building a multi-template atlas in a segmentation application. In the second experiment, we employ iCluster to compute multiple templates of a large data set that contains 416 brain MRI. Our results show that these templates correspond to different age groups.  We find the correlation between the image-based clustering, and demographic and clinical characteristics particularly intriguing, given the fact that iCluster did not employ the latter information.&lt;br /&gt;
&lt;br /&gt;
'''Experiment 1: Segmentation Label Alignment'''&lt;br /&gt;
&lt;br /&gt;
In this experiment, we used a data set of 50 whole brain MR brain images (of size 256x256x124 and voxel dimensions 0.9375x0.9375x1.5 mm) that&lt;br /&gt;
contained 16 patients with first episode schizophrenia (SZ), 17 patients with first-episode affective disorder (AFF) and 17 healthy subjects (CON). First episode patients are relatively free of chronicity-related confounds such as the long-term effects of medication, thus any structural differences between the three groups are subtle, local and difficult to identify in individual scans.&lt;br /&gt;
&lt;br /&gt;
The 50 MR images also contained manual labels of certain medial temporal lobe structures: the superior temporal gyrus (STG), hippocampus (HIPP), amygdala (AMY) and parahippocampal gyrus (PHG). We used these manual labels to explore label alignment across subjects under different groupings: on the whole data set, on random partitionings of the data set into two subsets of equal size, on the clinical grouping, and on the image-based clustering as determined by iCluster.&lt;br /&gt;
&lt;br /&gt;
[[Image:Two_templates_shenton50.png|center|600px|Two templates in a 50 subject MRI.]]&lt;br /&gt;
&lt;br /&gt;
We spatially normalized all the subjects into \textit{a standard space} using the iCluster algorithm with one-template and a 32x32x32 B-spline transformation model, and explored the alignment of the manual labels for clinical and image-based groupings. For each region of interest, such as amygdala, we computed the modified Haussdorff distance (MHD) in the standard space. MHD is a non -symmetric distance measure between the boundaries of two labels and is zero for perfect alignment.The MHD values for each region of interest were then summed up to obtain a total label distance for each ordered subject pair.&lt;br /&gt;
The following figure shows the total label distance for all subject pairings under the different groupings. We note that image-based clustering of iCluster (both with two-template and three-template)&lt;br /&gt;
groups subjects that have better label alignment, whereas the clinical grouping demonstrates no such coherence.&lt;br /&gt;
&lt;br /&gt;
[[Image:LabelAlignmentMatrixShenton50.png|center|600px|Label Alignment Matrices for the three groupings in the Shenton50 data set.]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
'''Experiment 2: Age groups in the OASIS data set'''&lt;br /&gt;
&lt;br /&gt;
In this experiment, we used the OASIS data set [http://www.oasis-brains.org] which consists of 416 pre-processed (skull stripped and gain-field corrected) brain MR images of subjects aged 18-96 years including individuals with early-stage Alzheimer's disease (AD). We ran iCluster on the whole data set while varying the number of templates from 2 through 6. Each run took approximately 4-8&lt;br /&gt;
hours on a 16 processor PC with 128GB RAM. For two- and three templates the algorithm computed unique and structurally different templates. We observed that these templates were robust: they were the same for random subsets of the data set of as little as 60 subjects. For larger number of templates, however, we observed that the computed templates were not all unique, or corresponded to single outlier subjects, or were not robust to random sub-sampling of the data set.&lt;br /&gt;
&lt;br /&gt;
The following figure shows the three robust templates computed by iCluster.&lt;br /&gt;
&lt;br /&gt;
[[Image:Three_templates_oasis.png|center|600px|Three templates of the OASIS data.]]&lt;br /&gt;
&lt;br /&gt;
The following figure shows the difference images between the three templates shown above.&lt;br /&gt;
&lt;br /&gt;
Difference_templates_oasis.png&lt;br /&gt;
&lt;br /&gt;
[[Image:Difference_templates_oasis.png|center|600px|Difference between the three templates of the OASIS data]]&lt;br /&gt;
 &lt;br /&gt;
The following figure includes the age distributions estimated using Parzen windowing with a Gaussian kernel and a s.t.d. of 4 years for each cluster identified by the algorithm.&lt;br /&gt;
&lt;br /&gt;
[[Image:Age_distributions_oasis.png|center|600px|Age groups in the OASIS data]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
'''Software'''&lt;br /&gt;
&lt;br /&gt;
The algorithm is currently implemented in the Insight ToolKit (ITK) and will be made publicly available. We also plan to integrate it into Slicer.&lt;br /&gt;
&lt;br /&gt;
= Key Investigators =&lt;br /&gt;
&lt;br /&gt;
MIT Algorithms: Mert R. Sabuncu, Serdar K. Balci and Polina Golland&lt;br /&gt;
&lt;br /&gt;
Harvard DBP 2: M.E. Shenton, M. Kubicki and S. Bouix&lt;br /&gt;
&lt;br /&gt;
= Publications =&lt;br /&gt;
&lt;br /&gt;
* NEW: Image-driven Population Analysis through Mixture-Modeling, M.R. Sabuncu, S.K. Balci, M.E. Shenton and P. Golland. IEEE Transactions on Medical Imaging. Accepted for Publication, 2009.&lt;br /&gt;
&lt;br /&gt;
* [http://www.na-mic.org/publications/pages/display?search=Projects%3AMultimodalAtlas&amp;amp;submit=Search&amp;amp;words=all&amp;amp;title=checked&amp;amp;keywords=checked&amp;amp;authors=checked&amp;amp;abstract=checked&amp;amp;sponsors=checked&amp;amp;searchbytag=checked| NA-MIC Publications Database]&lt;br /&gt;
&lt;br /&gt;
[[Category: Registration]]&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Algorithm:MIT&amp;diff=30898</id>
		<title>Algorithm:MIT</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Algorithm:MIT&amp;diff=30898"/>
		<updated>2008-10-09T22:11:58Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: /* Multimodal Atlas */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Back to [[Algorithm:Main|NA-MIC Algorithms]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
= Overview of MIT Algorithms (PI: Polina Golland) =&lt;br /&gt;
&lt;br /&gt;
Our group seeks to model statistical variability of anatomy and function across subjects and between populations and to utilize computational models of such variability to improve predictions for individual subjects, as well as characterize populations. Our long-term goal is to develop methods for joint modeling of anatomy and function and to apply them in clinical and scientific studies. We work primarily with anatomical, DTI and fMRI images. We actively contribute implementations of our algorithms to the NAMIC-kit.&lt;br /&gt;
&lt;br /&gt;
= MIT Projects =&lt;br /&gt;
&lt;br /&gt;
{| cellpadding=&amp;quot;10&amp;quot;&lt;br /&gt;
| style=&amp;quot;width:15%&amp;quot; | [[Image:Progress_Registration_Segmentation_Shape.jpg|200px]]&lt;br /&gt;
| style=&amp;quot;width:85%&amp;quot; | &lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeBasedSegmentationAndRegistration|Shape Based Segmentation and Registration]] ==&lt;br /&gt;
&lt;br /&gt;
This type of algorithm assigns a tissue type to each voxel in the volume. Incorporating prior shape information biases the label assignment towards contiguous regions that are consistent with the shape model. [[Projects:ShapeBasedSegmentationAndRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; K.M. Pohl, J. Fisher, S. Bouix, M. Shenton, R. W. McCarley, W.E.L. Grimson, R. Kikinis, and W.M. Wells. Using the Logarithm of Odds to Define a Vector Space on Probabilistic Atlases. Medical Image Analysis,11(6), pp. 465-477, 2007. &amp;lt;b&amp;gt;Best Paper Award MICCAI 2006 &amp;lt;/b&amp;gt;&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:JointRegSeg.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:RegistrationRegularization|Optimal Atlas Regularization in Image Segmentation]] ==&lt;br /&gt;
&lt;br /&gt;
We propose a unified framework for computing atlases from manually labeled data sets at various degrees of “sharpness” and the joint registration and segmentation of a new brain with these atlases. Using this framework, we investigate the tradeoff between warp regularization and image ﬁdelity, i.e. the smoothness of the new subject warp and the sharpness of the atlas in a segmentation application.&lt;br /&gt;
[[Projects:RegistrationRegularization|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; B.T.T. Yeo, M.R. Sabuncu, R. Desikan, B. Fischl, P. Golland. Effects of Registration Regularization and Atlas Sharpness on Segmentation Accuracy. Medical Image Analysis, 12(5):603--615, 2008. &lt;br /&gt;
  &lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:ICluster_templates.gif|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:MultimodalAtlas|Multimodal Atlas]] ==&lt;br /&gt;
&lt;br /&gt;
In this work, we propose and investigate an algorithm that jointly co-registers a collection of images while computing multiple templates. The algorithm, called '''iCluster''', is used to compute multiple atlases for a given population.&lt;br /&gt;
[[Projects:MultimodalAtlas|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; M.R. Sabuncu, Serdar K. Balci and Polina Golland. Discovering Modes of an Image Population through Mixture Modeling. MICCAI 2008. &lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:GroupwiseSummary.PNG|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:GroupwiseRegistration|Groupwise Registration]] ==&lt;br /&gt;
&lt;br /&gt;
We extend a previously demonstrated entropy based groupwise registration method to include a free-form deformation model based on B-splines. We provide an efficient implementation using stochastic gradient descents in a multi-resolution setting. We demonstrate the method in application to a set of 50 MRI brain scans and compare the results to a pairwise approach using segmentation labels to evaluate the quality of alignment.&lt;br /&gt;
[[Projects:GroupwiseRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
S.K. Balci, P. Golland, M.E. Shenton, W.M. Wells III. Free-Form B-spline Deformation Model for Groupwise Registration. In Proceedings of MICCAI 2007 Statistical Registration Workshop: Pair-wise and Group-wise Alignment and Atlas Formation, 23-30, 2007.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:FoldingSpeedDetection.png|200px|]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeAnalysisWithOvercompleteWavelets|Shape Analysis With Overcomplete Wavelets]] ==&lt;br /&gt;
&lt;br /&gt;
In this work, we extend the Euclidean wavelets to the sphere. The resulting over-complete spherical wavelets are invariant to the rotation of the spherical image parameterization. We apply the over-complete spherical wavelet to cortical folding development [[Projects:ShapeAnalysisWithOvercompleteWavelets|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; B.T.T. Yeo, P. Yu, P.E. Grant, B. Fischl, P. Golland. Shape Analysis with Overcomplete Spherical Wavelets. Proceedings of the International Conference on Medical Image Computing and Computer Assisted Intervention (MICCAI), volume 5241 of LNCS, 468--476, 2008&lt;br /&gt;
&lt;br /&gt;
B.T.T. Yeo, W. Ou, P. Golland. On the Construction of Invertible Filter Banks on the 2-Sphere. Yeo, Ou and Golland. IEEE Transactions on Image Processing. 17(3):283--300. 2008. &lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:MITHippocampalSubfieldSegmentation.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:HippocampalSubfieldSegmentation|Model-Based Segmentation of Hippocampal Subﬁelds in In Vivo MRI]] ==&lt;br /&gt;
&lt;br /&gt;
In this project we develop and validate a method for fully automated segmentation of the subfields of the hippocampus in ultra-high resolution in vivo MRI. [[Projects:HippocampalSubfieldSegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; K. Van Leemput, A. Bakkour, T. Benner, G. Wiggins, L.L. Wald, J. Augustinack, B.C. Dickerson, P. Golland, B. Fischl. Model-Based Segmentation of Hippocampal Subfields in Ultra-High Resolution In Vivo MRI. Accepted to MICCAI 2008. &lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| | [[Image:mit_fmri_clustering_parcellation2_xsub.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:fMRIClustering|fMRI clustering]] ==&lt;br /&gt;
&lt;br /&gt;
In this project we study the application of model-based clustering algorithms in identification of functional connectivity in the brain. [[Projects:fMRIClustering|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; D. Lashkari, N. Kanwisher, P. Golland. Discovering Structure in the Space of Activation&lt;br /&gt;
Profiles in fMRI. Accepted to MICCAI 2008. &lt;br /&gt;
  &lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:MIT_DTI_JointSegReg_atlas3D.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIFiberRegistration|Joint Registration and Segmentation of DWI Fiber Tractography]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this work is to jointly register and cluster DWI fiber tracts obtained from a group of subjects. [[Projects:DTIFiberRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; U. Ziyan, M. R. Sabuncu, W. E. L. Grimson, Carl-Fredrik Westin. A Robust Algorithm for Fiber-Bundle Atlas Construction. MMBIA 2007&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:brain.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIClustering|DTI Fiber Clustering and Fiber-Based Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this project is to provide structural description of the white matter architecture as a partition into coherent fiber bundles and clusters, and to use these bundles for quantitative measurement. [[Projects:DTIClustering|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; Monica E. Lemmond, Lauren J. O'Donnell, Stephen Whalen, Alexandra J. Golby. Characterizing Diffusion Along White Matter Tracts Affected by Primary Brain Tumors. Accepted to HBM 2007.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:Models.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIModeling|Fiber Tract Modeling, Clustering, and Quantitative Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this work is to model the shape of the fiber bundles and use this model description in clustering and statistical analysis of fiber tracts. [[Projects:DTIModeling|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; &lt;br /&gt;
&lt;br /&gt;
Mahnaz Maddah, Marek Kubicki, William M. Wells, Carl-Fredrik Westin, Martha E. Shenton and W. Eric L. Grimson, Findings in Schizophrenia by Tract-Oriented DT-MRI Analysis, to be presented in MICCAI 2008, NY, US.&lt;br /&gt;
&lt;br /&gt;
M. Maddah, L. Zollei, W. E. L. Grimson, W. M. Wells, Modeling of Anatomical Information in Clustering of White Matter Fiber Trajectories Using Dirichlet Distribution, to be presented at MMBIA 2008, Alaska, US.&lt;br /&gt;
&lt;br /&gt;
M. Maddah, L. Zollei, W. E. L. Grimson, C-F Westin, W. M. Wells, A Mathematical Framework for Incorporating Anatomical Knowledge in DT-MRI Analysis, ISBI 2008, Paris, France.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:FMRIEvaluationchart.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:fMRIDetection|fMRI Detection and Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
We are exploring algorithms for improved fMRI detection and interpretation by incorporting spatial priors and anatomical information to guide the detection. [[Projects:fMRIDetection|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; Wanmei Ou, Sandy Wells, Polina Golland. Bridging Spatial Regularization And Anatomical Priors in fMRI Detection. In preparation for submission to IEEE TMI. &lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:Thalamus_algo_outline.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTISegmentation|DTI-based Segmentation]] ==&lt;br /&gt;
&lt;br /&gt;
Unlike conventional MRI, DTI provides adequate contrast to segment the thalamic nuclei, which are gray matter structures. [[Projects:DTISegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; Ulas Ziyan, David Tuch, Carl-Fredrik Westin. Segmentation of Thalamic Nuclei from DTI using Spectral Clustering. Accepted to MICCAI 2006.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:ConnectivityMap.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIStochasticTractography|Stochastic Tractography]] ==&lt;br /&gt;
&lt;br /&gt;
This work calculates posterior distributions of white matter fiber tract parameters given diffusion observations in a DWI volume.  [[Projects:DTIStochasticTractography|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:HippocampalShapeDifferences.gif|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeAnalysis|Population Analysis of Anatomical Variability]] ==&lt;br /&gt;
&lt;br /&gt;
Our goal is to develop mathematical approaches to modeling anatomical variability within and across populations using tools like local shape descriptors of specific regions of interest and global constellation descriptors of multiple ROI's. [[Projects:ShapeAnalysis|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; Mert R Sabuncu and Polina Golland. Structural Constellations for Population Analysis of Anatomical Variability.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:MultimodalAtlas&amp;diff=30896</id>
		<title>Projects:MultimodalAtlas</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:MultimodalAtlas&amp;diff=30896"/>
		<updated>2008-10-09T22:11:18Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: /* Publications */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Back to [[NA-MIC_Internal_Collaborations:StructuralImageAnalysis|NA-MIC Collaborations]], [[Algorithm:MIT|MIT Algorithms]], [[DBP2:Harvard|Harvard DBP2]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
Today, computational anatomy studies are mainly hypothesis-driven, aiming to identify and characterize structural or functional differences between, for instance a group of patients with a specific disorder and control subjects. This type of approach has two premises: clinical classification of the subjects and spatial correspondence across the images. In practice, achieving either can be challenging. First, the complex spectrum of symptoms of neuro-degenerative disorders like schizophrenia and overlapping symptoms across different types of dementia like Alzheimer's disease, delirium and depression make a diagnosis based on standardized clinical tests like the mental status examination difficult. Second, across-subject correspondence in the images is a particularly hard problem that requires different approaches in various contexts. A popular technique is to normalize all subjects into a standard space, such as the Talairach space, by registering each image with a single, universal template image that represents an average brain. However, the quality of such an approach is limited by the accuracy with which the universal template represents the population in the study.&lt;br /&gt;
&lt;br /&gt;
With the increasing availability of medical images, data-driven algorithms offer the ability to probe a population and potentially discover sub-groups that may differ in unexpected ways. In this paper, we propose and demonstrate an efficient probabilistic clustering algorithm, called '''iCluster''', that:&lt;br /&gt;
&lt;br /&gt;
* computes a small number of templates that summarize a given population of images,&lt;br /&gt;
* simultaneously co-registers all the images using a nonlinear transformation model,&lt;br /&gt;
* assigns each input image to a template.&lt;br /&gt;
&lt;br /&gt;
The templates are guaranteed to live in an affine-normalized space, i.e., they are spatially aligned with respect to an affine transformation model.&lt;br /&gt;
&lt;br /&gt;
= Description =&lt;br /&gt;
&lt;br /&gt;
[[Image:GenerativeModel.png|center|400px|Generative Model used in iCluster.]]&lt;br /&gt;
&lt;br /&gt;
'''iCluster''' is derived from a simple generative model. We assume that there are a fixed and known number of template images. Then the process that generates an observed image is as follows: a template is randomly drawn – note that the probability that governs this process doesn’t have to be uniform. Next, the chosen template is warped with a random transformation and i.i.d Gaussian noise is added to this warped image to generate an observed image. This process is repeated multiple times to generate a collection of images.&lt;br /&gt;
&lt;br /&gt;
We formulate the problem as a maximum likelihood solution. We employ a Generalized Maximum Likelihood (GEM) algorithm to solve the problem. The GEM algorithm is derived using Jensen's inequality and has three steps: &lt;br /&gt;
*E-step: Given the estimates for the template images, template prior probabilities and noise variance image estimates from the previous iteration, the algorithm updates the memberships of each image as the posterior probability of an image being generated from a particular template.&lt;br /&gt;
*T-step: Given the membership estimates from the previous E-step, the algorithm updates the template image, template prior and noise variance estimates using closed-form expressions.&lt;br /&gt;
*R-step: Given the membership, template, template prior and noise variance estimates from the pervious iterations, the algorithm updates the warps for each image. This step is a collection of pairwise registration instances, where each image is aligned with an effective template image. The effective template image is a weighted average of the current individual templates, where the weights are current memberships.&lt;br /&gt;
&lt;br /&gt;
The resulting algorithm is fast and efficient: each iteration's time and memory requirements are linear in the number of voxels, input images and templates.&lt;br /&gt;
We employ a stochastic subsampling strategy in each one of the E, T and R steps. A random subsample of voxels (typically less than 1% of the total voxels) are used for the computations. &lt;br /&gt;
In the R-step, we employ a B-spline nonlinear transformation model and the optimization is done using gradient-descent. During this optimization, the gradients are normalized so that each cluster (i.e. the images assigned to the same template image) are subject to an average of zero deformation. This is an extension of the &amp;quot;anchoring&amp;quot; strategy used in groupwise registration algorithms. This is usually done by subtracting the average gradient from the individual gradients.&lt;br /&gt;
&lt;br /&gt;
= Results =&lt;br /&gt;
&lt;br /&gt;
We present two experiments. The first one demonstrates the use of iCluster for building a multi-template atlas in a segmentation application. In the second experiment, we employ iCluster to compute multiple templates of a large data set that contains 416 brain MRI. Our results show that these templates correspond to different age groups.  We find the correlation between the image-based clustering, and demographic and clinical characteristics particularly intriguing, given the fact that iCluster did not employ the latter information.&lt;br /&gt;
&lt;br /&gt;
'''Experiment 1: Segmentation Label Alignment'''&lt;br /&gt;
&lt;br /&gt;
In this experiment, we used a data set of 50 whole brain MR brain images (of size 256x256x124 and voxel dimensions 0.9375x0.9375x1.5 mm) that&lt;br /&gt;
contained 16 patients with first episode schizophrenia (SZ), 17 patients with first-episode affective disorder (AFF) and 17 healthy subjects (CON). First episode patients are relatively free of chronicity-related confounds such as the long-term effects of medication, thus any structural differences between the three groups are subtle, local and difficult to identify in individual scans.&lt;br /&gt;
&lt;br /&gt;
The 50 MR images also contained manual labels of certain medial temporal lobe structures: the superior temporal gyrus (STG), hippocampus (HIPP), amygdala (AMY) and parahippocampal gyrus (PHG). We used these manual labels to explore label alignment across subjects under different groupings: on the whole data set, on random partitionings of the data set into two subsets of equal size, on the clinical grouping, and on the image-based clustering as determined by iCluster.&lt;br /&gt;
&lt;br /&gt;
[[Image:Two_templates_shenton50.png|center|600px|Two templates in a 50 subject MRI.]]&lt;br /&gt;
&lt;br /&gt;
We spatially normalized all the subjects into \textit{a standard space} using the iCluster algorithm with one-template and a 32x32x32 B-spline transformation model, and explored the alignment of the manual labels for clinical and image-based groupings. For each region of interest, such as amygdala, we computed the modified Haussdorff distance (MHD) in the standard space. MHD is a non -symmetric distance measure between the boundaries of two labels and is zero for perfect alignment.The MHD values for each region of interest were then summed up to obtain a total label distance for each ordered subject pair.&lt;br /&gt;
The following figure shows the total label distance for all subject pairings under the different groupings. We note that image-based clustering of iCluster (both with two-template and three-template)&lt;br /&gt;
groups subjects that have better label alignment, whereas the clinical grouping demonstrates no such coherence.&lt;br /&gt;
&lt;br /&gt;
[[Image:LabelAlignmentMatrixShenton50.png|center|600px|Label Alignment Matrices for the three groupings in the Shenton50 data set.]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
'''Experiment 2: Age groups in the OASIS data set'''&lt;br /&gt;
&lt;br /&gt;
In this experiment, we used the OASIS data set [http://www.oasis-brains.org] which consists of 416 pre-processed (skull stripped and gain-field corrected) brain MR images of subjects aged 18-96 years including individuals with early-stage Alzheimer's disease (AD). We ran iCluster on the whole data set while varying the number of templates from 2 through 6. Each run took approximately 4-8&lt;br /&gt;
hours on a 16 processor PC with 128GB RAM. For two- and three templates the algorithm computed unique and structurally different templates. We observed that these templates were robust: they were the same for random subsets of the data set of as little as 60 subjects. For larger number of templates, however, we observed that the computed templates were not all unique, or corresponded to single outlier subjects, or were not robust to random sub-sampling of the data set.&lt;br /&gt;
&lt;br /&gt;
The following figure shows the three robust templates computed by iCluster.&lt;br /&gt;
&lt;br /&gt;
[[Image:Three_templates_oasis.png|center|600px|Three templates of the OASIS data.]]&lt;br /&gt;
&lt;br /&gt;
The following figure shows the difference images between the three templates shown above.&lt;br /&gt;
&lt;br /&gt;
Difference_templates_oasis.png&lt;br /&gt;
&lt;br /&gt;
[[Image:Difference_templates_oasis.png|center|600px|Difference between the three templates of the OASIS data]]&lt;br /&gt;
 &lt;br /&gt;
The following figure includes the age distributions estimated using Parzen windowing with a Gaussian kernel and a s.t.d. of 4 years for each cluster identified by the algorithm.&lt;br /&gt;
&lt;br /&gt;
[[Image:Age_distributions_oasis.png|center|600px|Age groups in the OASIS data]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
'''Software'''&lt;br /&gt;
&lt;br /&gt;
The algorithm is currently implemented in the Insight ToolKit (ITK) and will be made publicly available. We also plan to integrate it into Slicer.&lt;br /&gt;
&lt;br /&gt;
= Key Investigators =&lt;br /&gt;
&lt;br /&gt;
MIT Algorithms: Mert R. Sabuncu, Serdar K. Balci and Polina Golland&lt;br /&gt;
&lt;br /&gt;
Harvard DBP 2: M.E. Shenton, M. Kubicki and S. Bouix&lt;br /&gt;
&lt;br /&gt;
= Publications =&lt;br /&gt;
''In Print''&lt;br /&gt;
&lt;br /&gt;
* [http://www.na-mic.org/pages/Special:Publications?text=Projects%3AMultimodalAtlas&amp;amp;submit=Search&amp;amp;words=all&amp;amp;title=checked&amp;amp;keywords=checked&amp;amp;authors=checked&amp;amp;abstract=checked&amp;amp;sponsors=checked&amp;amp;searchbytag=checked| NA-MIC Publications Database]&lt;br /&gt;
&lt;br /&gt;
[[Category: Registration]]&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:MultimodalAtlas&amp;diff=30893</id>
		<title>Projects:MultimodalAtlas</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:MultimodalAtlas&amp;diff=30893"/>
		<updated>2008-10-09T22:07:20Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: /* Publications */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Back to [[NA-MIC_Internal_Collaborations:StructuralImageAnalysis|NA-MIC Collaborations]], [[Algorithm:MIT|MIT Algorithms]], [[DBP2:Harvard|Harvard DBP2]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
Today, computational anatomy studies are mainly hypothesis-driven, aiming to identify and characterize structural or functional differences between, for instance a group of patients with a specific disorder and control subjects. This type of approach has two premises: clinical classification of the subjects and spatial correspondence across the images. In practice, achieving either can be challenging. First, the complex spectrum of symptoms of neuro-degenerative disorders like schizophrenia and overlapping symptoms across different types of dementia like Alzheimer's disease, delirium and depression make a diagnosis based on standardized clinical tests like the mental status examination difficult. Second, across-subject correspondence in the images is a particularly hard problem that requires different approaches in various contexts. A popular technique is to normalize all subjects into a standard space, such as the Talairach space, by registering each image with a single, universal template image that represents an average brain. However, the quality of such an approach is limited by the accuracy with which the universal template represents the population in the study.&lt;br /&gt;
&lt;br /&gt;
With the increasing availability of medical images, data-driven algorithms offer the ability to probe a population and potentially discover sub-groups that may differ in unexpected ways. In this paper, we propose and demonstrate an efficient probabilistic clustering algorithm, called '''iCluster''', that:&lt;br /&gt;
&lt;br /&gt;
* computes a small number of templates that summarize a given population of images,&lt;br /&gt;
* simultaneously co-registers all the images using a nonlinear transformation model,&lt;br /&gt;
* assigns each input image to a template.&lt;br /&gt;
&lt;br /&gt;
The templates are guaranteed to live in an affine-normalized space, i.e., they are spatially aligned with respect to an affine transformation model.&lt;br /&gt;
&lt;br /&gt;
= Description =&lt;br /&gt;
&lt;br /&gt;
[[Image:GenerativeModel.png|center|400px|Generative Model used in iCluster.]]&lt;br /&gt;
&lt;br /&gt;
'''iCluster''' is derived from a simple generative model. We assume that there are a fixed and known number of template images. Then the process that generates an observed image is as follows: a template is randomly drawn – note that the probability that governs this process doesn’t have to be uniform. Next, the chosen template is warped with a random transformation and i.i.d Gaussian noise is added to this warped image to generate an observed image. This process is repeated multiple times to generate a collection of images.&lt;br /&gt;
&lt;br /&gt;
We formulate the problem as a maximum likelihood solution. We employ a Generalized Maximum Likelihood (GEM) algorithm to solve the problem. The GEM algorithm is derived using Jensen's inequality and has three steps: &lt;br /&gt;
*E-step: Given the estimates for the template images, template prior probabilities and noise variance image estimates from the previous iteration, the algorithm updates the memberships of each image as the posterior probability of an image being generated from a particular template.&lt;br /&gt;
*T-step: Given the membership estimates from the previous E-step, the algorithm updates the template image, template prior and noise variance estimates using closed-form expressions.&lt;br /&gt;
*R-step: Given the membership, template, template prior and noise variance estimates from the pervious iterations, the algorithm updates the warps for each image. This step is a collection of pairwise registration instances, where each image is aligned with an effective template image. The effective template image is a weighted average of the current individual templates, where the weights are current memberships.&lt;br /&gt;
&lt;br /&gt;
The resulting algorithm is fast and efficient: each iteration's time and memory requirements are linear in the number of voxels, input images and templates.&lt;br /&gt;
We employ a stochastic subsampling strategy in each one of the E, T and R steps. A random subsample of voxels (typically less than 1% of the total voxels) are used for the computations. &lt;br /&gt;
In the R-step, we employ a B-spline nonlinear transformation model and the optimization is done using gradient-descent. During this optimization, the gradients are normalized so that each cluster (i.e. the images assigned to the same template image) are subject to an average of zero deformation. This is an extension of the &amp;quot;anchoring&amp;quot; strategy used in groupwise registration algorithms. This is usually done by subtracting the average gradient from the individual gradients.&lt;br /&gt;
&lt;br /&gt;
= Results =&lt;br /&gt;
&lt;br /&gt;
We present two experiments. The first one demonstrates the use of iCluster for building a multi-template atlas in a segmentation application. In the second experiment, we employ iCluster to compute multiple templates of a large data set that contains 416 brain MRI. Our results show that these templates correspond to different age groups.  We find the correlation between the image-based clustering, and demographic and clinical characteristics particularly intriguing, given the fact that iCluster did not employ the latter information.&lt;br /&gt;
&lt;br /&gt;
'''Experiment 1: Segmentation Label Alignment'''&lt;br /&gt;
&lt;br /&gt;
In this experiment, we used a data set of 50 whole brain MR brain images (of size 256x256x124 and voxel dimensions 0.9375x0.9375x1.5 mm) that&lt;br /&gt;
contained 16 patients with first episode schizophrenia (SZ), 17 patients with first-episode affective disorder (AFF) and 17 healthy subjects (CON). First episode patients are relatively free of chronicity-related confounds such as the long-term effects of medication, thus any structural differences between the three groups are subtle, local and difficult to identify in individual scans.&lt;br /&gt;
&lt;br /&gt;
The 50 MR images also contained manual labels of certain medial temporal lobe structures: the superior temporal gyrus (STG), hippocampus (HIPP), amygdala (AMY) and parahippocampal gyrus (PHG). We used these manual labels to explore label alignment across subjects under different groupings: on the whole data set, on random partitionings of the data set into two subsets of equal size, on the clinical grouping, and on the image-based clustering as determined by iCluster.&lt;br /&gt;
&lt;br /&gt;
[[Image:Two_templates_shenton50.png|center|600px|Two templates in a 50 subject MRI.]]&lt;br /&gt;
&lt;br /&gt;
We spatially normalized all the subjects into \textit{a standard space} using the iCluster algorithm with one-template and a 32x32x32 B-spline transformation model, and explored the alignment of the manual labels for clinical and image-based groupings. For each region of interest, such as amygdala, we computed the modified Haussdorff distance (MHD) in the standard space. MHD is a non -symmetric distance measure between the boundaries of two labels and is zero for perfect alignment.The MHD values for each region of interest were then summed up to obtain a total label distance for each ordered subject pair.&lt;br /&gt;
The following figure shows the total label distance for all subject pairings under the different groupings. We note that image-based clustering of iCluster (both with two-template and three-template)&lt;br /&gt;
groups subjects that have better label alignment, whereas the clinical grouping demonstrates no such coherence.&lt;br /&gt;
&lt;br /&gt;
[[Image:LabelAlignmentMatrixShenton50.png|center|600px|Label Alignment Matrices for the three groupings in the Shenton50 data set.]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
'''Experiment 2: Age groups in the OASIS data set'''&lt;br /&gt;
&lt;br /&gt;
In this experiment, we used the OASIS data set [http://www.oasis-brains.org] which consists of 416 pre-processed (skull stripped and gain-field corrected) brain MR images of subjects aged 18-96 years including individuals with early-stage Alzheimer's disease (AD). We ran iCluster on the whole data set while varying the number of templates from 2 through 6. Each run took approximately 4-8&lt;br /&gt;
hours on a 16 processor PC with 128GB RAM. For two- and three templates the algorithm computed unique and structurally different templates. We observed that these templates were robust: they were the same for random subsets of the data set of as little as 60 subjects. For larger number of templates, however, we observed that the computed templates were not all unique, or corresponded to single outlier subjects, or were not robust to random sub-sampling of the data set.&lt;br /&gt;
&lt;br /&gt;
The following figure shows the three robust templates computed by iCluster.&lt;br /&gt;
&lt;br /&gt;
[[Image:Three_templates_oasis.png|center|600px|Three templates of the OASIS data.]]&lt;br /&gt;
&lt;br /&gt;
The following figure shows the difference images between the three templates shown above.&lt;br /&gt;
&lt;br /&gt;
Difference_templates_oasis.png&lt;br /&gt;
&lt;br /&gt;
[[Image:Difference_templates_oasis.png|center|600px|Difference between the three templates of the OASIS data]]&lt;br /&gt;
 &lt;br /&gt;
The following figure includes the age distributions estimated using Parzen windowing with a Gaussian kernel and a s.t.d. of 4 years for each cluster identified by the algorithm.&lt;br /&gt;
&lt;br /&gt;
[[Image:Age_distributions_oasis.png|center|600px|Age groups in the OASIS data]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
'''Software'''&lt;br /&gt;
&lt;br /&gt;
The algorithm is currently implemented in the Insight ToolKit (ITK) and will be made publicly available. We also plan to integrate it into Slicer.&lt;br /&gt;
&lt;br /&gt;
= Key Investigators =&lt;br /&gt;
&lt;br /&gt;
MIT Algorithms: Mert R. Sabuncu, Serdar K. Balci and Polina Golland&lt;br /&gt;
&lt;br /&gt;
Harvard DBP 2: M.E. Shenton, M. Kubicki and S. Bouix&lt;br /&gt;
&lt;br /&gt;
= Publications =&lt;br /&gt;
''In Print''&lt;br /&gt;
&lt;br /&gt;
* [http://www.na-mic.org/pages/Special:Publications?text=Projects%3AMultimodalAtlas&amp;amp;submit=Search&amp;amp;words=all&amp;amp;title=checked&amp;amp;keywords=checked&amp;amp;authors=checked&amp;amp;abstract=checked&amp;amp;sponsors=checked&amp;amp;searchbytag=checked| NA-MIC Publications Database]&lt;br /&gt;
&lt;br /&gt;
* [http://www.na-mic.org/pages/Special:Publications?text=Sabuncu+Discovering+Modes&amp;amp;submit=Search&amp;amp;words=all&amp;amp;title=checked&amp;amp;keywords=checked&amp;amp;authors=checked&amp;amp;abstract=checked&amp;amp;sponsors=checked&amp;amp;searchbytag=checked| NA-MIC Publications Database]&lt;br /&gt;
&lt;br /&gt;
[[Category: Registration]]&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:MultimodalAtlas&amp;diff=30892</id>
		<title>Projects:MultimodalAtlas</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:MultimodalAtlas&amp;diff=30892"/>
		<updated>2008-10-09T22:06:57Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: /* Publications */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Back to [[NA-MIC_Internal_Collaborations:StructuralImageAnalysis|NA-MIC Collaborations]], [[Algorithm:MIT|MIT Algorithms]], [[DBP2:Harvard|Harvard DBP2]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
Today, computational anatomy studies are mainly hypothesis-driven, aiming to identify and characterize structural or functional differences between, for instance a group of patients with a specific disorder and control subjects. This type of approach has two premises: clinical classification of the subjects and spatial correspondence across the images. In practice, achieving either can be challenging. First, the complex spectrum of symptoms of neuro-degenerative disorders like schizophrenia and overlapping symptoms across different types of dementia like Alzheimer's disease, delirium and depression make a diagnosis based on standardized clinical tests like the mental status examination difficult. Second, across-subject correspondence in the images is a particularly hard problem that requires different approaches in various contexts. A popular technique is to normalize all subjects into a standard space, such as the Talairach space, by registering each image with a single, universal template image that represents an average brain. However, the quality of such an approach is limited by the accuracy with which the universal template represents the population in the study.&lt;br /&gt;
&lt;br /&gt;
With the increasing availability of medical images, data-driven algorithms offer the ability to probe a population and potentially discover sub-groups that may differ in unexpected ways. In this paper, we propose and demonstrate an efficient probabilistic clustering algorithm, called '''iCluster''', that:&lt;br /&gt;
&lt;br /&gt;
* computes a small number of templates that summarize a given population of images,&lt;br /&gt;
* simultaneously co-registers all the images using a nonlinear transformation model,&lt;br /&gt;
* assigns each input image to a template.&lt;br /&gt;
&lt;br /&gt;
The templates are guaranteed to live in an affine-normalized space, i.e., they are spatially aligned with respect to an affine transformation model.&lt;br /&gt;
&lt;br /&gt;
= Description =&lt;br /&gt;
&lt;br /&gt;
[[Image:GenerativeModel.png|center|400px|Generative Model used in iCluster.]]&lt;br /&gt;
&lt;br /&gt;
'''iCluster''' is derived from a simple generative model. We assume that there are a fixed and known number of template images. Then the process that generates an observed image is as follows: a template is randomly drawn – note that the probability that governs this process doesn’t have to be uniform. Next, the chosen template is warped with a random transformation and i.i.d Gaussian noise is added to this warped image to generate an observed image. This process is repeated multiple times to generate a collection of images.&lt;br /&gt;
&lt;br /&gt;
We formulate the problem as a maximum likelihood solution. We employ a Generalized Maximum Likelihood (GEM) algorithm to solve the problem. The GEM algorithm is derived using Jensen's inequality and has three steps: &lt;br /&gt;
*E-step: Given the estimates for the template images, template prior probabilities and noise variance image estimates from the previous iteration, the algorithm updates the memberships of each image as the posterior probability of an image being generated from a particular template.&lt;br /&gt;
*T-step: Given the membership estimates from the previous E-step, the algorithm updates the template image, template prior and noise variance estimates using closed-form expressions.&lt;br /&gt;
*R-step: Given the membership, template, template prior and noise variance estimates from the pervious iterations, the algorithm updates the warps for each image. This step is a collection of pairwise registration instances, where each image is aligned with an effective template image. The effective template image is a weighted average of the current individual templates, where the weights are current memberships.&lt;br /&gt;
&lt;br /&gt;
The resulting algorithm is fast and efficient: each iteration's time and memory requirements are linear in the number of voxels, input images and templates.&lt;br /&gt;
We employ a stochastic subsampling strategy in each one of the E, T and R steps. A random subsample of voxels (typically less than 1% of the total voxels) are used for the computations. &lt;br /&gt;
In the R-step, we employ a B-spline nonlinear transformation model and the optimization is done using gradient-descent. During this optimization, the gradients are normalized so that each cluster (i.e. the images assigned to the same template image) are subject to an average of zero deformation. This is an extension of the &amp;quot;anchoring&amp;quot; strategy used in groupwise registration algorithms. This is usually done by subtracting the average gradient from the individual gradients.&lt;br /&gt;
&lt;br /&gt;
= Results =&lt;br /&gt;
&lt;br /&gt;
We present two experiments. The first one demonstrates the use of iCluster for building a multi-template atlas in a segmentation application. In the second experiment, we employ iCluster to compute multiple templates of a large data set that contains 416 brain MRI. Our results show that these templates correspond to different age groups.  We find the correlation between the image-based clustering, and demographic and clinical characteristics particularly intriguing, given the fact that iCluster did not employ the latter information.&lt;br /&gt;
&lt;br /&gt;
'''Experiment 1: Segmentation Label Alignment'''&lt;br /&gt;
&lt;br /&gt;
In this experiment, we used a data set of 50 whole brain MR brain images (of size 256x256x124 and voxel dimensions 0.9375x0.9375x1.5 mm) that&lt;br /&gt;
contained 16 patients with first episode schizophrenia (SZ), 17 patients with first-episode affective disorder (AFF) and 17 healthy subjects (CON). First episode patients are relatively free of chronicity-related confounds such as the long-term effects of medication, thus any structural differences between the three groups are subtle, local and difficult to identify in individual scans.&lt;br /&gt;
&lt;br /&gt;
The 50 MR images also contained manual labels of certain medial temporal lobe structures: the superior temporal gyrus (STG), hippocampus (HIPP), amygdala (AMY) and parahippocampal gyrus (PHG). We used these manual labels to explore label alignment across subjects under different groupings: on the whole data set, on random partitionings of the data set into two subsets of equal size, on the clinical grouping, and on the image-based clustering as determined by iCluster.&lt;br /&gt;
&lt;br /&gt;
[[Image:Two_templates_shenton50.png|center|600px|Two templates in a 50 subject MRI.]]&lt;br /&gt;
&lt;br /&gt;
We spatially normalized all the subjects into \textit{a standard space} using the iCluster algorithm with one-template and a 32x32x32 B-spline transformation model, and explored the alignment of the manual labels for clinical and image-based groupings. For each region of interest, such as amygdala, we computed the modified Haussdorff distance (MHD) in the standard space. MHD is a non -symmetric distance measure between the boundaries of two labels and is zero for perfect alignment.The MHD values for each region of interest were then summed up to obtain a total label distance for each ordered subject pair.&lt;br /&gt;
The following figure shows the total label distance for all subject pairings under the different groupings. We note that image-based clustering of iCluster (both with two-template and three-template)&lt;br /&gt;
groups subjects that have better label alignment, whereas the clinical grouping demonstrates no such coherence.&lt;br /&gt;
&lt;br /&gt;
[[Image:LabelAlignmentMatrixShenton50.png|center|600px|Label Alignment Matrices for the three groupings in the Shenton50 data set.]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
'''Experiment 2: Age groups in the OASIS data set'''&lt;br /&gt;
&lt;br /&gt;
In this experiment, we used the OASIS data set [http://www.oasis-brains.org] which consists of 416 pre-processed (skull stripped and gain-field corrected) brain MR images of subjects aged 18-96 years including individuals with early-stage Alzheimer's disease (AD). We ran iCluster on the whole data set while varying the number of templates from 2 through 6. Each run took approximately 4-8&lt;br /&gt;
hours on a 16 processor PC with 128GB RAM. For two- and three templates the algorithm computed unique and structurally different templates. We observed that these templates were robust: they were the same for random subsets of the data set of as little as 60 subjects. For larger number of templates, however, we observed that the computed templates were not all unique, or corresponded to single outlier subjects, or were not robust to random sub-sampling of the data set.&lt;br /&gt;
&lt;br /&gt;
The following figure shows the three robust templates computed by iCluster.&lt;br /&gt;
&lt;br /&gt;
[[Image:Three_templates_oasis.png|center|600px|Three templates of the OASIS data.]]&lt;br /&gt;
&lt;br /&gt;
The following figure shows the difference images between the three templates shown above.&lt;br /&gt;
&lt;br /&gt;
Difference_templates_oasis.png&lt;br /&gt;
&lt;br /&gt;
[[Image:Difference_templates_oasis.png|center|600px|Difference between the three templates of the OASIS data]]&lt;br /&gt;
 &lt;br /&gt;
The following figure includes the age distributions estimated using Parzen windowing with a Gaussian kernel and a s.t.d. of 4 years for each cluster identified by the algorithm.&lt;br /&gt;
&lt;br /&gt;
[[Image:Age_distributions_oasis.png|center|600px|Age groups in the OASIS data]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
'''Software'''&lt;br /&gt;
&lt;br /&gt;
The algorithm is currently implemented in the Insight ToolKit (ITK) and will be made publicly available. We also plan to integrate it into Slicer.&lt;br /&gt;
&lt;br /&gt;
= Key Investigators =&lt;br /&gt;
&lt;br /&gt;
MIT Algorithms: Mert R. Sabuncu, Serdar K. Balci and Polina Golland&lt;br /&gt;
&lt;br /&gt;
Harvard DBP 2: M.E. Shenton, M. Kubicki and S. Bouix&lt;br /&gt;
&lt;br /&gt;
= Publications =&lt;br /&gt;
''In Print''&lt;br /&gt;
&lt;br /&gt;
* [http://www.na-mic.org/pages/Special:Publications?text=Projects%3AMultimodalAtlas&amp;amp;submit=Search&amp;amp;words=all&amp;amp;title=checked&amp;amp;keywords=checked&amp;amp;authors=checked&amp;amp;abstract=checked&amp;amp;sponsors=checked&amp;amp;searchbytag=checked| NA-MIC Publications Database]&lt;br /&gt;
|&lt;br /&gt;
* [http://www.na-mic.org/pages/Special:Publications?text=Sabuncu+Discovering+Modes&amp;amp;submit=Search&amp;amp;words=all&amp;amp;title=checked&amp;amp;keywords=checked&amp;amp;authors=checked&amp;amp;abstract=checked&amp;amp;sponsors=checked&amp;amp;searchbytag=checked| NA-MIC Publications Database]&lt;br /&gt;
&lt;br /&gt;
[[Category: Registration]]&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:MultimodalAtlas&amp;diff=30887</id>
		<title>Projects:MultimodalAtlas</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:MultimodalAtlas&amp;diff=30887"/>
		<updated>2008-10-09T22:02:41Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: /* Publications */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Back to [[NA-MIC_Internal_Collaborations:StructuralImageAnalysis|NA-MIC Collaborations]], [[Algorithm:MIT|MIT Algorithms]], [[DBP2:Harvard|Harvard DBP2]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
Today, computational anatomy studies are mainly hypothesis-driven, aiming to identify and characterize structural or functional differences between, for instance a group of patients with a specific disorder and control subjects. This type of approach has two premises: clinical classification of the subjects and spatial correspondence across the images. In practice, achieving either can be challenging. First, the complex spectrum of symptoms of neuro-degenerative disorders like schizophrenia and overlapping symptoms across different types of dementia like Alzheimer's disease, delirium and depression make a diagnosis based on standardized clinical tests like the mental status examination difficult. Second, across-subject correspondence in the images is a particularly hard problem that requires different approaches in various contexts. A popular technique is to normalize all subjects into a standard space, such as the Talairach space, by registering each image with a single, universal template image that represents an average brain. However, the quality of such an approach is limited by the accuracy with which the universal template represents the population in the study.&lt;br /&gt;
&lt;br /&gt;
With the increasing availability of medical images, data-driven algorithms offer the ability to probe a population and potentially discover sub-groups that may differ in unexpected ways. In this paper, we propose and demonstrate an efficient probabilistic clustering algorithm, called '''iCluster''', that:&lt;br /&gt;
&lt;br /&gt;
* computes a small number of templates that summarize a given population of images,&lt;br /&gt;
* simultaneously co-registers all the images using a nonlinear transformation model,&lt;br /&gt;
* assigns each input image to a template.&lt;br /&gt;
&lt;br /&gt;
The templates are guaranteed to live in an affine-normalized space, i.e., they are spatially aligned with respect to an affine transformation model.&lt;br /&gt;
&lt;br /&gt;
= Description =&lt;br /&gt;
&lt;br /&gt;
[[Image:GenerativeModel.png|center|400px|Generative Model used in iCluster.]]&lt;br /&gt;
&lt;br /&gt;
'''iCluster''' is derived from a simple generative model. We assume that there are a fixed and known number of template images. Then the process that generates an observed image is as follows: a template is randomly drawn – note that the probability that governs this process doesn’t have to be uniform. Next, the chosen template is warped with a random transformation and i.i.d Gaussian noise is added to this warped image to generate an observed image. This process is repeated multiple times to generate a collection of images.&lt;br /&gt;
&lt;br /&gt;
We formulate the problem as a maximum likelihood solution. We employ a Generalized Maximum Likelihood (GEM) algorithm to solve the problem. The GEM algorithm is derived using Jensen's inequality and has three steps: &lt;br /&gt;
*E-step: Given the estimates for the template images, template prior probabilities and noise variance image estimates from the previous iteration, the algorithm updates the memberships of each image as the posterior probability of an image being generated from a particular template.&lt;br /&gt;
*T-step: Given the membership estimates from the previous E-step, the algorithm updates the template image, template prior and noise variance estimates using closed-form expressions.&lt;br /&gt;
*R-step: Given the membership, template, template prior and noise variance estimates from the pervious iterations, the algorithm updates the warps for each image. This step is a collection of pairwise registration instances, where each image is aligned with an effective template image. The effective template image is a weighted average of the current individual templates, where the weights are current memberships.&lt;br /&gt;
&lt;br /&gt;
The resulting algorithm is fast and efficient: each iteration's time and memory requirements are linear in the number of voxels, input images and templates.&lt;br /&gt;
We employ a stochastic subsampling strategy in each one of the E, T and R steps. A random subsample of voxels (typically less than 1% of the total voxels) are used for the computations. &lt;br /&gt;
In the R-step, we employ a B-spline nonlinear transformation model and the optimization is done using gradient-descent. During this optimization, the gradients are normalized so that each cluster (i.e. the images assigned to the same template image) are subject to an average of zero deformation. This is an extension of the &amp;quot;anchoring&amp;quot; strategy used in groupwise registration algorithms. This is usually done by subtracting the average gradient from the individual gradients.&lt;br /&gt;
&lt;br /&gt;
= Results =&lt;br /&gt;
&lt;br /&gt;
We present two experiments. The first one demonstrates the use of iCluster for building a multi-template atlas in a segmentation application. In the second experiment, we employ iCluster to compute multiple templates of a large data set that contains 416 brain MRI. Our results show that these templates correspond to different age groups.  We find the correlation between the image-based clustering, and demographic and clinical characteristics particularly intriguing, given the fact that iCluster did not employ the latter information.&lt;br /&gt;
&lt;br /&gt;
'''Experiment 1: Segmentation Label Alignment'''&lt;br /&gt;
&lt;br /&gt;
In this experiment, we used a data set of 50 whole brain MR brain images (of size 256x256x124 and voxel dimensions 0.9375x0.9375x1.5 mm) that&lt;br /&gt;
contained 16 patients with first episode schizophrenia (SZ), 17 patients with first-episode affective disorder (AFF) and 17 healthy subjects (CON). First episode patients are relatively free of chronicity-related confounds such as the long-term effects of medication, thus any structural differences between the three groups are subtle, local and difficult to identify in individual scans.&lt;br /&gt;
&lt;br /&gt;
The 50 MR images also contained manual labels of certain medial temporal lobe structures: the superior temporal gyrus (STG), hippocampus (HIPP), amygdala (AMY) and parahippocampal gyrus (PHG). We used these manual labels to explore label alignment across subjects under different groupings: on the whole data set, on random partitionings of the data set into two subsets of equal size, on the clinical grouping, and on the image-based clustering as determined by iCluster.&lt;br /&gt;
&lt;br /&gt;
[[Image:Two_templates_shenton50.png|center|600px|Two templates in a 50 subject MRI.]]&lt;br /&gt;
&lt;br /&gt;
We spatially normalized all the subjects into \textit{a standard space} using the iCluster algorithm with one-template and a 32x32x32 B-spline transformation model, and explored the alignment of the manual labels for clinical and image-based groupings. For each region of interest, such as amygdala, we computed the modified Haussdorff distance (MHD) in the standard space. MHD is a non -symmetric distance measure between the boundaries of two labels and is zero for perfect alignment.The MHD values for each region of interest were then summed up to obtain a total label distance for each ordered subject pair.&lt;br /&gt;
The following figure shows the total label distance for all subject pairings under the different groupings. We note that image-based clustering of iCluster (both with two-template and three-template)&lt;br /&gt;
groups subjects that have better label alignment, whereas the clinical grouping demonstrates no such coherence.&lt;br /&gt;
&lt;br /&gt;
[[Image:LabelAlignmentMatrixShenton50.png|center|600px|Label Alignment Matrices for the three groupings in the Shenton50 data set.]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
'''Experiment 2: Age groups in the OASIS data set'''&lt;br /&gt;
&lt;br /&gt;
In this experiment, we used the OASIS data set [http://www.oasis-brains.org] which consists of 416 pre-processed (skull stripped and gain-field corrected) brain MR images of subjects aged 18-96 years including individuals with early-stage Alzheimer's disease (AD). We ran iCluster on the whole data set while varying the number of templates from 2 through 6. Each run took approximately 4-8&lt;br /&gt;
hours on a 16 processor PC with 128GB RAM. For two- and three templates the algorithm computed unique and structurally different templates. We observed that these templates were robust: they were the same for random subsets of the data set of as little as 60 subjects. For larger number of templates, however, we observed that the computed templates were not all unique, or corresponded to single outlier subjects, or were not robust to random sub-sampling of the data set.&lt;br /&gt;
&lt;br /&gt;
The following figure shows the three robust templates computed by iCluster.&lt;br /&gt;
&lt;br /&gt;
[[Image:Three_templates_oasis.png|center|600px|Three templates of the OASIS data.]]&lt;br /&gt;
&lt;br /&gt;
The following figure shows the difference images between the three templates shown above.&lt;br /&gt;
&lt;br /&gt;
Difference_templates_oasis.png&lt;br /&gt;
&lt;br /&gt;
[[Image:Difference_templates_oasis.png|center|600px|Difference between the three templates of the OASIS data]]&lt;br /&gt;
 &lt;br /&gt;
The following figure includes the age distributions estimated using Parzen windowing with a Gaussian kernel and a s.t.d. of 4 years for each cluster identified by the algorithm.&lt;br /&gt;
&lt;br /&gt;
[[Image:Age_distributions_oasis.png|center|600px|Age groups in the OASIS data]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
'''Software'''&lt;br /&gt;
&lt;br /&gt;
The algorithm is currently implemented in the Insight ToolKit (ITK) and will be made publicly available. We also plan to integrate it into Slicer.&lt;br /&gt;
&lt;br /&gt;
= Key Investigators =&lt;br /&gt;
&lt;br /&gt;
MIT Algorithms: Mert R. Sabuncu, Serdar K. Balci and Polina Golland&lt;br /&gt;
&lt;br /&gt;
Harvard DBP 2: M.E. Shenton, M. Kubicki and S. Bouix&lt;br /&gt;
&lt;br /&gt;
= Publications =&lt;br /&gt;
''In Print''&lt;br /&gt;
&lt;br /&gt;
* [http://www.na-mic.org/pages/Special:Publications?text=Projects%3AMultimodalAtlas&amp;amp;submit=Search&amp;amp;words=all&amp;amp;title=checked&amp;amp;keywords=checked&amp;amp;authors=checked&amp;amp;abstract=checked&amp;amp;sponsors=checked&amp;amp;searchbytag=checked| NA-MIC Publications Database]&lt;br /&gt;
&lt;br /&gt;
* [http://www.na-mic.org/pages/Special:PubDB_View?dspaceid=1452]&lt;br /&gt;
&lt;br /&gt;
[[Category: Registration]]&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Algorithm:MIT&amp;diff=24776</id>
		<title>Algorithm:MIT</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Algorithm:MIT&amp;diff=24776"/>
		<updated>2008-05-16T21:36:13Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Back to [[Algorithm:Main|NA-MIC Algorithms]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
= Overview of MIT Algorithms =&lt;br /&gt;
&lt;br /&gt;
Our group seeks to model statistical variability of anatomy and function across subjects and between populations and to utilize computational models of such variability to improve predictions for individual subjects, as well as characterize populations. Our long-term goal is to develop methods for joint modeling of anatomy and function and to apply them in clinical and scientific studies. We work primarily with anatomical, DTI and fMRI images. We actively contribute implementations of our algorithms to the NAMIC-kit.&lt;br /&gt;
&lt;br /&gt;
= MIT Projects =&lt;br /&gt;
&lt;br /&gt;
{| cellpadding=&amp;quot;10&amp;quot;&lt;br /&gt;
| style=&amp;quot;width:15%&amp;quot; | [[Image:Progress_Registration_Segmentation_Shape.jpg|200px]]&lt;br /&gt;
| style=&amp;quot;width:85%&amp;quot; | &lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeBasedSegmentationAndRegistration|Shape Based Segmentation and Registration]] ==&lt;br /&gt;
&lt;br /&gt;
This type of algorithm assigns a tissue type to each voxel in the volume. Incorporating prior shape information biases the label assignment towards contiguous regions that are consistent with the shape model. [[Projects:ShapeBasedSegmentationAndRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; K.M. Pohl, J. Fisher, S. Bouix, M. Shenton, R. W. McCarley, W.E.L. Grimson, R. Kikinis, and W.M. Wells. Using the Logarithm of Odds to Define a Vector Space on Probabilistic Atlases. Medical Image Analysis,11(6), pp. 465-477, 2007. &amp;lt;b&amp;gt;Best Paper Award MICCAI 2006 &amp;lt;/b&amp;gt;&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:JointRegSeg.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:RegistrationRegularization|Optimal Atlas Regularization in Image Segmentation]] ==&lt;br /&gt;
&lt;br /&gt;
We propose a unified framework for computing atlases from manually labeled data sets at various degrees of “sharpness” and the joint registration and segmentation of a new brain with these atlases. Using this framework, we investigate the tradeoff between warp regularization and image ﬁdelity, i.e. the smoothness of the new subject warp and the sharpness of the atlas in a segmentation application.&lt;br /&gt;
[[Projects:RegistrationRegularization|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; B.T.T. Yeo, M.R. Sabuncu, R. Desikan, B. Fischl, P. Golland. Effects of Registration Regularization and Atlas Sharpness on Segmentation Accuracy. In Proceedings of MICCAI: International Conference on Medical Image Computing and Computer Assisted Intervention, 683-691, 2007. '''MICCAI Young Scientist Award.'''&lt;br /&gt;
  &lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:ICluster_templates.gif|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:MultimodalAtlas|Multimodal Atlas]] ==&lt;br /&gt;
&lt;br /&gt;
In this work, we propose and investigate an algorithm that jointly co-registers a collection of images while computing multiple templates. The algorithm, called '''iCluster''', is used to compute multiple atlases for a given population.&lt;br /&gt;
[[Projects:MultimodalAtlas|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; M.R. Sabuncu, Serdar K. Balci and Polina Golland. Discovering Modes of an Image Population through Mixture. Accepted to MICCAI 2008. &lt;br /&gt;
'''In Press:''' M.R. Sabuncu, M.E. Shenton, P. Golland. Joint Registration and Clustering of Images. In Proceedings of MICCAI 2007 Statistical Registration Workshop: Pair-wise and Group-wise Alignment and Atlas Formation, 47-54, 2007.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:GroupwiseSummary.PNG|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:GroupwiseRegistration|Groupwise Registration]] ==&lt;br /&gt;
&lt;br /&gt;
We extend a previously demonstrated entropy based groupwise registration method to include a free-form deformation model based on B-splines. We provide an efficient implementation using stochastic gradient descents in a multi-resolution setting. We demonstrate the method in application to a set of 50 MRI brain scans and compare the results to a pairwise approach using segmentation labels to evaluate the quality of alignment.&lt;br /&gt;
[[Projects:GroupwiseRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
S.K. Balci, P. Golland, M.E. Shenton, W.M. Wells III. Free-Form B-spline Deformation Model for Groupwise Registration. In Proceedings of MICCAI 2007 Statistical Registration Workshop: Pair-wise and Group-wise Alignment and Atlas Formation, 23-30, 2007.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:FoldingSpeedDetection.png|200px|]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeAnalysisWithOvercompleteWavelets|Shape Analysis With Overcomplete Wavelets]] ==&lt;br /&gt;
&lt;br /&gt;
In this work, we extend the Euclidean wavelets to the sphere. The resulting over-complete spherical wavelets are invariant to the rotation of the spherical image parameterization. We apply the over-complete spherical wavelet to cortical folding development [[Projects:ShapeAnalysisWithOvercompleteWavelets|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; B.T.T. Yeo, W. Ou, P. Golland. On the Construction of Invertible Filter Banks on the 2-Sphere. Yeo, Ou and Golland. Accepted to the IEEE Transactions on Image Processing. &lt;br /&gt;
&lt;br /&gt;
P. Yu, B.T.T. Yeo, P.E. Grant, B. Fischl, P. Golland. Cortical Folding Development Study based on Over-Complete Spherical Wavelets. In Proceedings of MMBIA: IEEE Computer Society Workshop on Mathematical Methods in Biomedical Image Analysis, 2007.&lt;br /&gt;
  &lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:mit_fmri_clustering_parcellation2_xsub.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:fMRIClustering|fMRI clustering]] ==&lt;br /&gt;
&lt;br /&gt;
In this project we study the application of model-based clustering algorithms in identification of functional connectivity in the brain. [[Projects:fMRIClustering|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; P. Golland, Y. Golland, R. Malach. Detection of Spatial Activation Patterns As Unsupervised Segmentation of fMRI Data. In Proceedings of MICCAI: International Conference on Medical Image Computing and Computer Assisted Intervention, 110-118, 2007. &lt;br /&gt;
  &lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:MIT_DTI_JointSegReg_atlas3D.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIFiberRegistration|Joint Registration and Segmentation of DWI Fiber Tractography]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this work is to jointly register and cluster DWI fiber tracts obtained from a group of subjects. [[Projects:DTIFiberRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; U. Ziyan, M. R. Sabuncu, W. E. L. Grimson, Carl-Fredrik Westin. A Robust Algorithm for Fiber-Bundle Atlas Construction. MMBIA 2007&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:brain.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIClustering|DTI Fiber Clustering and Fiber-Based Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this project is to provide structural description of the white matter architecture as a partition into coherent fiber bundles and clusters, and to use these bundles for quantitative measurement. [[Projects:DTIClustering|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; Monica E. Lemmond, Lauren J. O'Donnell, Stephen Whalen, Alexandra J. Golby. Characterizing Diffusion Along White Matter Tracts Affected by Primary Brain Tumors. Accepted to HBM 2007.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:Models.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIModeling|Fiber Tract Modeling, Clustering, and Quantitative Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this work is to model the shape of the fiber bundles and use this model discription in clustering and statistical analysis of fiber tracts. [[Projects:DTIModeling|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; &lt;br /&gt;
M. Maddah, W. E. L. Grimson, S. K. Warfield, W. M. Wells, A Unified Framework for Clustering and Quantitative Analysis of White Matter Fiber Tracts. Medical Image Analysis, in press. &lt;br /&gt;
&lt;br /&gt;
M. Maddah, W. M. Wells, S. K. Warfield, C.-F. Westin, and W. E. L. Grimson, Probabilistic Clustering and Quantitative Analysis of White Matter Fiber Tracts, IPMI 2007, Netherlands.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:FMRIEvaluationchart.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:fMRIDetection|fMRI Detection and Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
We are exploring algorithms for improved fMRI detection and interpretation by incorporting spatial priors and anatomical information to guide the detection. [[Projects:fMRIDetection|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; Wanmei Ou, Sandy Wells, Polina Golland. Bridging Spatial Regularization And Anatomical Priors in fMRI Detection. In preparation for submission to IEEE TMI. &lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:Thalamus_algo_outline.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTISegmentation|DTI-based Segmentation]] ==&lt;br /&gt;
&lt;br /&gt;
Unlike conventional MRI, DTI provides adequate contrast to segment the thalamic nuclei, which are gray matter structures. [[Projects:DTISegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; Ulas Ziyan, David Tuch, Carl-Fredrik Westin. Segmentation of Thalamic Nuclei from DTI using Spectral Clustering. Accepted to MICCAI 2006.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:ConnectivityMap.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIStochasticTractography|Stochastic Tractography]] ==&lt;br /&gt;
&lt;br /&gt;
This work calculates posterior distributions of white matter fiber tract parameters given diffusion observations in a DWI volume.  [[Projects:DTIStochasticTractography|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:HippocampalShapeDifferences.gif|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeAnalysis|Population Analysis of Anatomical Variability]] ==&lt;br /&gt;
&lt;br /&gt;
Our goal is to develop mathematical approaches to modeling anatomical variability within and across populations using tools like local shape descriptors of specific regions of interest and global constellation descriptors of multiple ROI's. [[Projects:ShapeAnalysis|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; Mert R Sabuncu and Polina Golland. Structural Constellations for Population Analysis of Anatomical Variability.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== [[Projects:HippocampalSubfieldSegmentation|Model-Based Segmentation of Hippocampal Subﬁelds in In Vivo MRI]] ==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Algorithm:MIT&amp;diff=24774</id>
		<title>Algorithm:MIT</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Algorithm:MIT&amp;diff=24774"/>
		<updated>2008-05-16T21:35:49Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Back to [[Algorithm:Main|NA-MIC Algorithms]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
= Overview of MIT Algorithms =&lt;br /&gt;
&lt;br /&gt;
Our group seeks to model statistical variability of anatomy and function across subjects and between populations and to utilize computational models of such variability to improve predictions for individual subjects, as well as characterize populations. Our long-term goal is to develop methods for joint modeling of anatomy and function and to apply them in clinical and scientific studies. We work primarily with anatomical, DTI and fMRI images. We actively contribute implementations of our algorithms to the NAMIC-kit.&lt;br /&gt;
&lt;br /&gt;
= MIT Projects =&lt;br /&gt;
&lt;br /&gt;
{| cellpadding=&amp;quot;10&amp;quot;&lt;br /&gt;
| style=&amp;quot;width:15%&amp;quot; | [[Image:Progress_Registration_Segmentation_Shape.jpg|200px]]&lt;br /&gt;
| style=&amp;quot;width:85%&amp;quot; | &lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeBasedSegmentationAndRegistration|Shape Based Segmentation and Registration]] ==&lt;br /&gt;
&lt;br /&gt;
This type of algorithm assigns a tissue type to each voxel in the volume. Incorporating prior shape information biases the label assignment towards contiguous regions that are consistent with the shape model. [[Projects:ShapeBasedSegmentationAndRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; K.M. Pohl, J. Fisher, S. Bouix, M. Shenton, R. W. McCarley, W.E.L. Grimson, R. Kikinis, and W.M. Wells. Using the Logarithm of Odds to Define a Vector Space on Probabilistic Atlases. Medical Image Analysis,11(6), pp. 465-477, 2007. &amp;lt;b&amp;gt;Best Paper Award MICCAI 2006 &amp;lt;/b&amp;gt;&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:JointRegSeg.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:RegistrationRegularization|Optimal Atlas Regularization in Image Segmentation]] ==&lt;br /&gt;
&lt;br /&gt;
We propose a unified framework for computing atlases from manually labeled data sets at various degrees of “sharpness” and the joint registration and segmentation of a new brain with these atlases. Using this framework, we investigate the tradeoff between warp regularization and image ﬁdelity, i.e. the smoothness of the new subject warp and the sharpness of the atlas in a segmentation application.&lt;br /&gt;
[[Projects:RegistrationRegularization|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; B.T.T. Yeo, M.R. Sabuncu, R. Desikan, B. Fischl, P. Golland. Effects of Registration Regularization and Atlas Sharpness on Segmentation Accuracy. In Proceedings of MICCAI: International Conference on Medical Image Computing and Computer Assisted Intervention, 683-691, 2007. '''MICCAI Young Scientist Award.'''&lt;br /&gt;
  &lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:ICluster_templates.gif|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:MultimodalAtlas|Multimodal Atlas]] ==&lt;br /&gt;
&lt;br /&gt;
In this work, we propose and investigate an algorithm that jointly co-registers a collection of images while computing multiple templates. The algorithm, called '''iCluster''', is used to compute multiple atlases for a given population.&lt;br /&gt;
[[Projects:MultimodalAtlas|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; M.R. Sabuncu, Serdar K. Balci and Polina Golland. Discovering Modes of an Image Population through Mixture. Accepted to MICCAI 2008. &lt;br /&gt;
'''In Press''' M.R. Sabuncu, M.E. Shenton, P. Golland. Joint Registration and Clustering of Images. In Proceedings of MICCAI 2007 Statistical Registration Workshop: Pair-wise and Group-wise Alignment and Atlas Formation, 47-54, 2007.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:GroupwiseSummary.PNG|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:GroupwiseRegistration|Groupwise Registration]] ==&lt;br /&gt;
&lt;br /&gt;
We extend a previously demonstrated entropy based groupwise registration method to include a free-form deformation model based on B-splines. We provide an efficient implementation using stochastic gradient descents in a multi-resolution setting. We demonstrate the method in application to a set of 50 MRI brain scans and compare the results to a pairwise approach using segmentation labels to evaluate the quality of alignment.&lt;br /&gt;
[[Projects:GroupwiseRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
S.K. Balci, P. Golland, M.E. Shenton, W.M. Wells III. Free-Form B-spline Deformation Model for Groupwise Registration. In Proceedings of MICCAI 2007 Statistical Registration Workshop: Pair-wise and Group-wise Alignment and Atlas Formation, 23-30, 2007.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:FoldingSpeedDetection.png|200px|]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeAnalysisWithOvercompleteWavelets|Shape Analysis With Overcomplete Wavelets]] ==&lt;br /&gt;
&lt;br /&gt;
In this work, we extend the Euclidean wavelets to the sphere. The resulting over-complete spherical wavelets are invariant to the rotation of the spherical image parameterization. We apply the over-complete spherical wavelet to cortical folding development [[Projects:ShapeAnalysisWithOvercompleteWavelets|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; B.T.T. Yeo, W. Ou, P. Golland. On the Construction of Invertible Filter Banks on the 2-Sphere. Yeo, Ou and Golland. Accepted to the IEEE Transactions on Image Processing. &lt;br /&gt;
&lt;br /&gt;
P. Yu, B.T.T. Yeo, P.E. Grant, B. Fischl, P. Golland. Cortical Folding Development Study based on Over-Complete Spherical Wavelets. In Proceedings of MMBIA: IEEE Computer Society Workshop on Mathematical Methods in Biomedical Image Analysis, 2007.&lt;br /&gt;
  &lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:mit_fmri_clustering_parcellation2_xsub.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:fMRIClustering|fMRI clustering]] ==&lt;br /&gt;
&lt;br /&gt;
In this project we study the application of model-based clustering algorithms in identification of functional connectivity in the brain. [[Projects:fMRIClustering|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New: '''&amp;lt;/font&amp;gt; P. Golland, Y. Golland, R. Malach. Detection of Spatial Activation Patterns As Unsupervised Segmentation of fMRI Data. In Proceedings of MICCAI: International Conference on Medical Image Computing and Computer Assisted Intervention, 110-118, 2007. &lt;br /&gt;
  &lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:MIT_DTI_JointSegReg_atlas3D.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIFiberRegistration|Joint Registration and Segmentation of DWI Fiber Tractography]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this work is to jointly register and cluster DWI fiber tracts obtained from a group of subjects. [[Projects:DTIFiberRegistration|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; U. Ziyan, M. R. Sabuncu, W. E. L. Grimson, Carl-Fredrik Westin. A Robust Algorithm for Fiber-Bundle Atlas Construction. MMBIA 2007&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:brain.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIClustering|DTI Fiber Clustering and Fiber-Based Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this project is to provide structural description of the white matter architecture as a partition into coherent fiber bundles and clusters, and to use these bundles for quantitative measurement. [[Projects:DTIClustering|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; Monica E. Lemmond, Lauren J. O'Donnell, Stephen Whalen, Alexandra J. Golby. Characterizing Diffusion Along White Matter Tracts Affected by Primary Brain Tumors. Accepted to HBM 2007.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:Models.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIModeling|Fiber Tract Modeling, Clustering, and Quantitative Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
The goal of this work is to model the shape of the fiber bundles and use this model discription in clustering and statistical analysis of fiber tracts. [[Projects:DTIModeling|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; &lt;br /&gt;
M. Maddah, W. E. L. Grimson, S. K. Warfield, W. M. Wells, A Unified Framework for Clustering and Quantitative Analysis of White Matter Fiber Tracts. Medical Image Analysis, in press. &lt;br /&gt;
&lt;br /&gt;
M. Maddah, W. M. Wells, S. K. Warfield, C.-F. Westin, and W. E. L. Grimson, Probabilistic Clustering and Quantitative Analysis of White Matter Fiber Tracts, IPMI 2007, Netherlands.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:FMRIEvaluationchart.jpg|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:fMRIDetection|fMRI Detection and Analysis]] ==&lt;br /&gt;
&lt;br /&gt;
We are exploring algorithms for improved fMRI detection and interpretation by incorporting spatial priors and anatomical information to guide the detection. [[Projects:fMRIDetection|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; Wanmei Ou, Sandy Wells, Polina Golland. Bridging Spatial Regularization And Anatomical Priors in fMRI Detection. In preparation for submission to IEEE TMI. &lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:Thalamus_algo_outline.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTISegmentation|DTI-based Segmentation]] ==&lt;br /&gt;
&lt;br /&gt;
Unlike conventional MRI, DTI provides adequate contrast to segment the thalamic nuclei, which are gray matter structures. [[Projects:DTISegmentation|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; Ulas Ziyan, David Tuch, Carl-Fredrik Westin. Segmentation of Thalamic Nuclei from DTI using Spectral Clustering. Accepted to MICCAI 2006.&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:ConnectivityMap.png|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:DTIStochasticTractography|Stochastic Tractography]] ==&lt;br /&gt;
&lt;br /&gt;
This work calculates posterior distributions of white matter fiber tract parameters given diffusion observations in a DWI volume.  [[Projects:DTIStochasticTractography|More...]]&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| | [[Image:HippocampalShapeDifferences.gif|200px]]&lt;br /&gt;
| |&lt;br /&gt;
&lt;br /&gt;
== [[Projects:ShapeAnalysis|Population Analysis of Anatomical Variability]] ==&lt;br /&gt;
&lt;br /&gt;
Our goal is to develop mathematical approaches to modeling anatomical variability within and across populations using tools like local shape descriptors of specific regions of interest and global constellation descriptors of multiple ROI's. [[Projects:ShapeAnalysis|More...]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;font color=&amp;quot;red&amp;quot;&amp;gt;'''New:'''&amp;lt;/font&amp;gt; Mert R Sabuncu and Polina Golland. Structural Constellations for Population Analysis of Anatomical Variability.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== [[Projects:HippocampalSubfieldSegmentation|Model-Based Segmentation of Hippocampal Subﬁelds in In Vivo MRI]] ==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:MultimodalAtlas&amp;diff=24772</id>
		<title>Projects:MultimodalAtlas</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:MultimodalAtlas&amp;diff=24772"/>
		<updated>2008-05-16T21:32:45Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Back to [[NA-MIC_Internal_Collaborations:StructuralImageAnalysis|NA-MIC Collaborations]], [[Algorithm:MIT|MIT Algorithms]], [[DBP2:Harvard|Harvard DBP2]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
Today, computational anatomy studies are mainly hypothesis-driven, aiming to identify and characterize structural or functional differences between, for instance a group of patients with a specific disorder and control subjects. This type of approach has two premises: clinical classification of the subjects and spatial correspondence across the images. In practice, achieving either can be challenging. First, the complex spectrum of symptoms of neuro-degenerative disorders like schizophrenia and overlapping symptoms across different types of dementia like Alzheimer's disease, delirium and depression make a diagnosis based on standardized clinical tests like the mental status examination difficult. Second, across-subject correspondence in the images is a particularly hard problem that requires different approaches in various contexts. A popular technique is to normalize all subjects into a standard space, such as the Talairach space, by registering each image with a single, universal template image that represents an average brain. However, the quality of such an approach is limited by the accuracy with which the universal template represents the population in the study.&lt;br /&gt;
&lt;br /&gt;
With the increasing availability of medical images, data-driven algorithms offer the ability to probe a population and potentially discover sub-groups that may differ in unexpected ways. In this paper, we propose and demonstrate an efficient probabilistic clustering algorithm, called '''iCluster''', that:&lt;br /&gt;
&lt;br /&gt;
* computes a small number of templates that summarize a given population of images,&lt;br /&gt;
* simultaneously co-registers all the images using a nonlinear transformation model,&lt;br /&gt;
* assigns each input image to a template.&lt;br /&gt;
&lt;br /&gt;
The templates are guaranteed to live in an affine-normalized space, i.e., they are spatially aligned with respect to an affine transformation model.&lt;br /&gt;
&lt;br /&gt;
= Description =&lt;br /&gt;
&lt;br /&gt;
[[Image:GenerativeModel.png|center|400px|Generative Model used in iCluster.]]&lt;br /&gt;
&lt;br /&gt;
'''iCluster''' is derived from a simple generative model. We assume that there are a fixed and known number of template images. Then the process that generates an observed image is as follows: a template is randomly drawn – note that the probability that governs this process doesn’t have to be uniform. Next, the chosen template is warped with a random transformation and i.i.d Gaussian noise is added to this warped image to generate an observed image. This process is repeated multiple times to generate a collection of images.&lt;br /&gt;
&lt;br /&gt;
We formulate the problem as a maximum likelihood solution. We employ a Generalized Maximum Likelihood (GEM) algorithm to solve the problem. The GEM algorithm is derived using Jensen's inequality and has three steps: &lt;br /&gt;
*E-step: Given the estimates for the template images, template prior probabilities and noise variance image estimates from the previous iteration, the algorithm updates the memberships of each image as the posterior probability of an image being generated from a particular template.&lt;br /&gt;
*T-step: Given the membership estimates from the previous E-step, the algorithm updates the template image, template prior and noise variance estimates using closed-form expressions.&lt;br /&gt;
*R-step: Given the membership, template, template prior and noise variance estimates from the pervious iterations, the algorithm updates the warps for each image. This step is a collection of pairwise registration instances, where each image is aligned with an effective template image. The effective template image is a weighted average of the current individual templates, where the weights are current memberships.&lt;br /&gt;
&lt;br /&gt;
The resulting algorithm is fast and efficient: each iteration's time and memory requirements are linear in the number of voxels, input images and templates.&lt;br /&gt;
We employ a stochastic subsampling strategy in each one of the E, T and R steps. A random subsample of voxels (typically less than 1% of the total voxels) are used for the computations. &lt;br /&gt;
In the R-step, we employ a B-spline nonlinear transformation model and the optimization is done using gradient-descent. During this optimization, the gradients are normalized so that each cluster (i.e. the images assigned to the same template image) are subject to an average of zero deformation. This is an extension of the &amp;quot;anchoring&amp;quot; strategy used in groupwise registration algorithms. This is usually done by subtracting the average gradient from the individual gradients.&lt;br /&gt;
&lt;br /&gt;
= Results =&lt;br /&gt;
&lt;br /&gt;
We present two experiments. The first one demonstrates the use of iCluster for building a multi-template atlas in a segmentation application. In the second experiment, we employ iCluster to compute multiple templates of a large data set that contains 416 brain MRI. Our results show that these templates correspond to different age groups.  We find the correlation between the image-based clustering, and demographic and clinical characteristics particularly intriguing, given the fact that iCluster did not employ the latter information.&lt;br /&gt;
&lt;br /&gt;
'''Experiment 1: Segmentation Label Alignment'''&lt;br /&gt;
&lt;br /&gt;
In this experiment, we used a data set of 50 whole brain MR brain images (of size 256x256x124 and voxel dimensions 0.9375x0.9375x1.5 mm) that&lt;br /&gt;
contained 16 patients with first episode schizophrenia (SZ), 17 patients with first-episode affective disorder (AFF) and 17 healthy subjects (CON). First episode patients are relatively free of chronicity-related confounds such as the long-term effects of medication, thus any structural differences between the three groups are subtle, local and difficult to identify in individual scans.&lt;br /&gt;
&lt;br /&gt;
The 50 MR images also contained manual labels of certain medial temporal lobe structures: the superior temporal gyrus (STG), hippocampus (HIPP), amygdala (AMY) and parahippocampal gyrus (PHG). We used these manual labels to explore label alignment across subjects under different groupings: on the whole data set, on random partitionings of the data set into two subsets of equal size, on the clinical grouping, and on the image-based clustering as determined by iCluster.&lt;br /&gt;
&lt;br /&gt;
[[Image:Two_templates_shenton50.png|center|600px|Two templates in a 50 subject MRI.]]&lt;br /&gt;
&lt;br /&gt;
We spatially normalized all the subjects into \textit{a standard space} using the iCluster algorithm with one-template and a 32x32x32 B-spline transformation model, and explored the alignment of the manual labels for clinical and image-based groupings. For each region of interest, such as amygdala, we computed the modified Haussdorff distance (MHD) in the standard space. MHD is a non -symmetric distance measure between the boundaries of two labels and is zero for perfect alignment.The MHD values for each region of interest were then summed up to obtain a total label distance for each ordered subject pair.&lt;br /&gt;
The following figure shows the total label distance for all subject pairings under the different groupings. We note that image-based clustering of iCluster (both with two-template and three-template)&lt;br /&gt;
groups subjects that have better label alignment, whereas the clinical grouping demonstrates no such coherence.&lt;br /&gt;
&lt;br /&gt;
[[Image:LabelAlignmentMatrixShenton50.png|center|600px|Label Alignment Matrices for the three groupings in the Shenton50 data set.]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
'''Experiment 2: Age groups in the OASIS data set'''&lt;br /&gt;
&lt;br /&gt;
In this experiment, we used the OASIS data set [http://www.oasis-brains.org] which consists of 416 pre-processed (skull stripped and gain-field corrected) brain MR images of subjects aged 18-96 years including individuals with early-stage Alzheimer's disease (AD). We ran iCluster on the whole data set while varying the number of templates from 2 through 6. Each run took approximately 4-8&lt;br /&gt;
hours on a 16 processor PC with 128GB RAM. For two- and three templates the algorithm computed unique and structurally different templates. We observed that these templates were robust: they were the same for random subsets of the data set of as little as 60 subjects. For larger number of templates, however, we observed that the computed templates were not all unique, or corresponded to single outlier subjects, or were not robust to random sub-sampling of the data set.&lt;br /&gt;
&lt;br /&gt;
The following figure shows the three robust templates computed by iCluster.&lt;br /&gt;
&lt;br /&gt;
[[Image:Three_templates_oasis.png|center|600px|Three templates of the OASIS data.]]&lt;br /&gt;
&lt;br /&gt;
The following figure shows the difference images between the three templates shown above.&lt;br /&gt;
&lt;br /&gt;
Difference_templates_oasis.png&lt;br /&gt;
&lt;br /&gt;
[[Image:Difference_templates_oasis.png|center|600px|Difference between the three templates of the OASIS data]]&lt;br /&gt;
 &lt;br /&gt;
The following figure includes the age distributions estimated using Parzen windowing with a Gaussian kernel and a s.t.d. of 4 years for each cluster identified by the algorithm.&lt;br /&gt;
&lt;br /&gt;
[[Image:Age_distributions_oasis.png|center|600px|Age groups in the OASIS data]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
'''Software'''&lt;br /&gt;
&lt;br /&gt;
The algorithm is currently implemented in the Insight ToolKit (ITK) and will be made publicly available. We also plan to integrate it into Slicer.&lt;br /&gt;
&lt;br /&gt;
= Key Investigators =&lt;br /&gt;
&lt;br /&gt;
MIT Algorithms: Mert R. Sabuncu, Serdar K. Balci and Polina Golland&lt;br /&gt;
&lt;br /&gt;
Harvard DBP 2: M.E. Shenton, M. Kubicki and S. Bouix&lt;br /&gt;
&lt;br /&gt;
= Publications =&lt;br /&gt;
''New''&lt;br /&gt;
&lt;br /&gt;
Discovering the Modes of an Image Population through Mixture Modeling, Mert R Sabuncu, Serdar Balci, and Polina Golland. Accepted to MICCAI '08.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''In Print''&lt;br /&gt;
&lt;br /&gt;
* [http://www.na-mic.org/pages/Special:Publications?text=multimodal+sabuncu&amp;amp;submit=Search&amp;amp;words=all&amp;amp;title=checked&amp;amp;keywords=checked&amp;amp;authors=checked&amp;amp;abstract=checked&amp;amp;sponsors=checked&amp;amp;searchbytag=checked| NA-MIC Publications Database]&lt;br /&gt;
&lt;br /&gt;
[[Category: Registration]]&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:MultimodalAtlas&amp;diff=24771</id>
		<title>Projects:MultimodalAtlas</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:MultimodalAtlas&amp;diff=24771"/>
		<updated>2008-05-16T21:32:20Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Back to [[NA-MIC_Internal_Collaborations:StructuralImageAnalysis|NA-MIC Collaborations]], [[Algorithm:MIT|MIT Algorithms]], [[DBP2:Harvard|Harvard DBP2]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
Today, computational anatomy studies are mainly hypothesis-driven, aiming to identify and characterize structural or functional differences between, for instance a group of patients with a specific disorder and control subjects. This type of approach has two premises: clinical classification of the subjects and spatial correspondence across the images. In practice, achieving either can be challenging. First, the complex spectrum of symptoms of neuro-degenerative disorders like schizophrenia and overlapping symptoms across different types of dementia like Alzheimer's disease, delirium and depression make a diagnosis based on standardized clinical tests like the mental status examination difficult. Second, across-subject correspondence in the images is a particularly hard problem that requires different approaches in various contexts. A popular technique is to normalize all subjects into a standard space, such as the Talairach space, by registering each image with a single, universal template image that represents an average brain. However, the quality of such an approach is limited by the accuracy with which the universal template represents the population in the study.&lt;br /&gt;
&lt;br /&gt;
With the increasing availability of medical images, data-driven algorithms offer the ability to probe a population and potentially discover sub-groups that may differ in unexpected ways. In this paper, we propose and demonstrate an efficient probabilistic clustering algorithm, called '''iCluster''', that:&lt;br /&gt;
&lt;br /&gt;
* computes a small number of templates that summarize a given population of images,&lt;br /&gt;
* simultaneously co-registers all the images using a nonlinear transformation model,&lt;br /&gt;
* assigns each input image to a template.&lt;br /&gt;
&lt;br /&gt;
The templates are guaranteed to live in an affine-normalized space, i.e., they are spatially aligned with respect to an affine transformation model.&lt;br /&gt;
&lt;br /&gt;
= Description =&lt;br /&gt;
&lt;br /&gt;
[[Image:GenerativeModel.png|center|400px|Generative Model used in iCluster.]]&lt;br /&gt;
&lt;br /&gt;
'''iCluster''' is derived from a simple generative model. We assume that there are a fixed and known number of template images. Then the process that generates an observed image is as follows: a template is randomly drawn – note that the probability that governs this process doesn’t have to be uniform. Next, the chosen template is warped with a random transformation and i.i.d Gaussian noise is added to this warped image to generate an observed image. This process is repeated multiple times to generate a collection of images.&lt;br /&gt;
&lt;br /&gt;
We formulate the problem as a maximum likelihood solution. We employ a Generalized Maximum Likelihood (GEM) algorithm to solve the problem. The GEM algorithm is derived using Jensen's inequality and has three steps: &lt;br /&gt;
*E-step: Given the estimates for the template images, template prior probabilities and noise variance image estimates from the previous iteration, the algorithm updates the memberships of each image as the posterior probability of an image being generated from a particular template.&lt;br /&gt;
*T-step: Given the membership estimates from the previous E-step, the algorithm updates the template image, template prior and noise variance estimates using closed-form expressions.&lt;br /&gt;
*R-step: Given the membership, template, template prior and noise variance estimates from the pervious iterations, the algorithm updates the warps for each image. This step is a collection of pairwise registration instances, where each image is aligned with an effective template image. The effective template image is a weighted average of the current individual templates, where the weights are current memberships.&lt;br /&gt;
&lt;br /&gt;
The resulting algorithm is fast and efficient: each iteration's time and memory requirements are linear in the number of voxels, input images and templates.&lt;br /&gt;
We employ a stochastic subsampling strategy in each one of the E, T and R steps. A random subsample of voxels (typically less than 1% of the total voxels) are used for the computations. &lt;br /&gt;
In the R-step, we employ a B-spline nonlinear transformation model and the optimization is done using gradient-descent. During this optimization, the gradients are normalized so that each cluster (i.e. the images assigned to the same template image) are subject to an average of zero deformation. This is an extension of the &amp;quot;anchoring&amp;quot; strategy used in groupwise registration algorithms. This is usually done by subtracting the average gradient from the individual gradients.&lt;br /&gt;
&lt;br /&gt;
= Results =&lt;br /&gt;
&lt;br /&gt;
We present two experiments. The first one demonstrates the use of iCluster for building a multi-template atlas in a segmentation application. In the second experiment, we employ iCluster to compute multiple templates of a large data set that contains 416 brain MRI. Our results show that these templates correspond to different age groups.  We find the correlation between the image-based clustering, and demographic and clinical characteristics particularly intriguing, given the fact that iCluster did not employ the latter information.&lt;br /&gt;
&lt;br /&gt;
'''Experiment 1: Segmentation Label Alignment'''&lt;br /&gt;
&lt;br /&gt;
In this experiment, we used a data set of 50 whole brain MR brain images (of size 256x256x124 and voxel dimensions 0.9375x0.9375x1.5 mm) that&lt;br /&gt;
contained 16 patients with first episode schizophrenia (SZ), 17 patients with first-episode affective disorder (AFF) and 17 healthy subjects (CON). First episode patients are relatively free of chronicity-related confounds such as the long-term effects of medication, thus any structural differences between the three groups are subtle, local and difficult to identify in individual scans.&lt;br /&gt;
&lt;br /&gt;
The 50 MR images also contained manual labels of certain medial temporal lobe structures: the superior temporal gyrus (STG), hippocampus (HIPP), amygdala (AMY) and parahippocampal gyrus (PHG). We used these manual labels to explore label alignment across subjects under different groupings: on the whole data set, on random partitionings of the data set into two subsets of equal size, on the clinical grouping, and on the image-based clustering as determined by iCluster.&lt;br /&gt;
&lt;br /&gt;
[[Image:Two_templates_shenton50.png|center|600px|Two templates in a 50 subject MRI.]]&lt;br /&gt;
&lt;br /&gt;
We spatially normalized all the subjects into \textit{a standard space} using the iCluster algorithm with one-template and a 32x32x32 B-spline transformation model, and explored the alignment of the manual labels for clinical and image-based groupings. For each region of interest, such as amygdala, we computed the modified Haussdorff distance (MHD) in the standard space. MHD is a non -symmetric distance measure between the boundaries of two labels and is zero for perfect alignment.The MHD values for each region of interest were then summed up to obtain a total label distance for each ordered subject pair.&lt;br /&gt;
The following figure shows the total label distance for all subject pairings under the different groupings. We note that image-based clustering of iCluster (both with two-template and three-template)&lt;br /&gt;
groups subjects that have better label alignment, whereas the clinical grouping demonstrates no such coherence.&lt;br /&gt;
&lt;br /&gt;
[[Image:LabelAlignmentMatrixShenton50.png|center|600px|Label Alignment Matrices for the three groupings in the Shenton50 data set.]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
'''Experiment 2: Age groups in the OASIS data set'''&lt;br /&gt;
&lt;br /&gt;
In this experiment, we used the OASIS data set [http://www.oasis-brains.org] which consists of 416 pre-processed (skull stripped and gain-field corrected) brain MR images of subjects aged 18-96 years including individuals with early-stage Alzheimer's disease (AD). We ran iCluster on the whole data set while varying the number of templates from 2 through 6. Each run took approximately 4-8&lt;br /&gt;
hours on a 16 processor PC with 128GB RAM. For two- and three templates the algorithm computed unique and structurally different templates. We observed that these templates were robust: they were the same for random subsets of the data set of as little as 60 subjects. For larger number of templates, however, we observed that the computed templates were not all unique, or corresponded to single outlier subjects, or were not robust to random sub-sampling of the data set.&lt;br /&gt;
&lt;br /&gt;
The following figure shows the three robust templates computed by iCluster.&lt;br /&gt;
&lt;br /&gt;
[[Image:Three_templates_oasis.png|center|600px|Three templates of the OASIS data.]]&lt;br /&gt;
&lt;br /&gt;
The following figure shows the difference images between the three templates shown above.&lt;br /&gt;
&lt;br /&gt;
Difference_templates_oasis.png&lt;br /&gt;
&lt;br /&gt;
[[Image:Difference_templates_oasis.png|center|600px|Difference between the three templates of the OASIS data]]&lt;br /&gt;
 &lt;br /&gt;
The following figure includes the age distributions estimated using Parzen windowing with a Gaussian kernel and a s.t.d. of 4 years for each cluster identified by the algorithm.&lt;br /&gt;
&lt;br /&gt;
[[Image:Age_distributions_oasis.png|center|600px|Age groups in the OASIS data]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
'''Software'''&lt;br /&gt;
&lt;br /&gt;
The algorithm is currently implemented in the Insight ToolKit (ITK) and will be made publicly available. We also plan to integrate it into Slicer.&lt;br /&gt;
&lt;br /&gt;
= Key Investigators =&lt;br /&gt;
&lt;br /&gt;
MIT Algorithms: Mert R. Sabuncu, Serdar K. Balci and Polina Golland&lt;br /&gt;
&lt;br /&gt;
Harvard DBP 2: M.E. Shenton, M. Kubicki and S. Bouix&lt;br /&gt;
&lt;br /&gt;
= Publications =&lt;br /&gt;
''New''&lt;br /&gt;
&lt;br /&gt;
Discovering the Modes of an Image Population through Mixture Modeling, Mert R Sabuncu, Serdar Balci, and Polina Golland. Accepted to MICCAI '08.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''In Print''&lt;br /&gt;
&lt;br /&gt;
* [http://www.na-mic.org/pages/Special:Publications?text=multimodal+sabuncu&amp;amp;sub&lt;br /&gt;
mit=Search&amp;amp;words=all&amp;amp;title=checked&amp;amp;keywords=checked&amp;amp;authors=checked&amp;amp;abstract&lt;br /&gt;
=checked&amp;amp;sponsors=checked&amp;amp;searchbytag=checked| NA-MIC Publications Database]&lt;br /&gt;
&lt;br /&gt;
[[Category: Registration]]&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:MultimodalAtlas&amp;diff=24770</id>
		<title>Projects:MultimodalAtlas</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:MultimodalAtlas&amp;diff=24770"/>
		<updated>2008-05-16T21:31:47Z</updated>

		<summary type="html">&lt;p&gt;Msabuncu: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Back to [[NA-MIC_Internal_Collaborations:StructuralImageAnalysis|NA-MIC Collaborations]], [[Algorithm:MIT|MIT Algorithms]], [[DBP2:Harvard|Harvard DBP2]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
Today, computational anatomy studies are mainly hypothesis-driven, aiming to identify and characterize structural or functional differences between, for instance a group of patients with a specific disorder and control subjects. This type of approach has two premises: clinical classification of the subjects and spatial correspondence across the images. In practice, achieving either can be challenging. First, the complex spectrum of symptoms of neuro-degenerative disorders like schizophrenia and overlapping symptoms across different types of dementia like Alzheimer's disease, delirium and depression make a diagnosis based on standardized clinical tests like the mental status examination difficult. Second, across-subject correspondence in the images is a particularly hard problem that requires different approaches in various contexts. A popular technique is to normalize all subjects into a standard space, such as the Talairach space, by registering each image with a single, universal template image that represents an average brain. However, the quality of such an approach is limited by the accuracy with which the universal template represents the population in the study.&lt;br /&gt;
&lt;br /&gt;
With the increasing availability of medical images, data-driven algorithms offer the ability to probe a population and potentially discover sub-groups that may differ in unexpected ways. In this paper, we propose and demonstrate an efficient probabilistic clustering algorithm, called '''iCluster''', that:&lt;br /&gt;
&lt;br /&gt;
* computes a small number of templates that summarize a given population of images,&lt;br /&gt;
* simultaneously co-registers all the images using a nonlinear transformation model,&lt;br /&gt;
* assigns each input image to a template.&lt;br /&gt;
&lt;br /&gt;
The templates are guaranteed to live in an affine-normalized space, i.e., they are spatially aligned with respect to an affine transformation model.&lt;br /&gt;
&lt;br /&gt;
= Description =&lt;br /&gt;
&lt;br /&gt;
[[Image:GenerativeModel.png|center|400px|Generative Model used in iCluster.]]&lt;br /&gt;
&lt;br /&gt;
'''iCluster''' is derived from a simple generative model. We assume that there are a fixed and known number of template images. Then the process that generates an observed image is as follows: a template is randomly drawn – note that the probability that governs this process doesn’t have to be uniform. Next, the chosen template is warped with a random transformation and i.i.d Gaussian noise is added to this warped image to generate an observed image. This process is repeated multiple times to generate a collection of images.&lt;br /&gt;
&lt;br /&gt;
We formulate the problem as a maximum likelihood solution. We employ a Generalized Maximum Likelihood (GEM) algorithm to solve the problem. The GEM algorithm is derived using Jensen's inequality and has three steps: &lt;br /&gt;
*E-step: Given the estimates for the template images, template prior probabilities and noise variance image estimates from the previous iteration, the algorithm updates the memberships of each image as the posterior probability of an image being generated from a particular template.&lt;br /&gt;
*T-step: Given the membership estimates from the previous E-step, the algorithm updates the template image, template prior and noise variance estimates using closed-form expressions.&lt;br /&gt;
*R-step: Given the membership, template, template prior and noise variance estimates from the pervious iterations, the algorithm updates the warps for each image. This step is a collection of pairwise registration instances, where each image is aligned with an effective template image. The effective template image is a weighted average of the current individual templates, where the weights are current memberships.&lt;br /&gt;
&lt;br /&gt;
The resulting algorithm is fast and efficient: each iteration's time and memory requirements are linear in the number of voxels, input images and templates.&lt;br /&gt;
We employ a stochastic subsampling strategy in each one of the E, T and R steps. A random subsample of voxels (typically less than 1% of the total voxels) are used for the computations. &lt;br /&gt;
In the R-step, we employ a B-spline nonlinear transformation model and the optimization is done using gradient-descent. During this optimization, the gradients are normalized so that each cluster (i.e. the images assigned to the same template image) are subject to an average of zero deformation. This is an extension of the &amp;quot;anchoring&amp;quot; strategy used in groupwise registration algorithms. This is usually done by subtracting the average gradient from the individual gradients.&lt;br /&gt;
&lt;br /&gt;
= Results =&lt;br /&gt;
&lt;br /&gt;
We present two experiments. The first one demonstrates the use of iCluster for building a multi-template atlas in a segmentation application. In the second experiment, we employ iCluster to compute multiple templates of a large data set that contains 416 brain MRI. Our results show that these templates correspond to different age groups.  We find the correlation between the image-based clustering, and demographic and clinical characteristics particularly intriguing, given the fact that iCluster did not employ the latter information.&lt;br /&gt;
&lt;br /&gt;
'''Experiment 1: Segmentation Label Alignment'''&lt;br /&gt;
&lt;br /&gt;
In this experiment, we used a data set of 50 whole brain MR brain images (of size 256x256x124 and voxel dimensions 0.9375x0.9375x1.5 mm) that&lt;br /&gt;
contained 16 patients with first episode schizophrenia (SZ), 17 patients with first-episode affective disorder (AFF) and 17 healthy subjects (CON). First episode patients are relatively free of chronicity-related confounds such as the long-term effects of medication, thus any structural differences between the three groups are subtle, local and difficult to identify in individual scans.&lt;br /&gt;
&lt;br /&gt;
The 50 MR images also contained manual labels of certain medial temporal lobe structures: the superior temporal gyrus (STG), hippocampus (HIPP), amygdala (AMY) and parahippocampal gyrus (PHG). We used these manual labels to explore label alignment across subjects under different groupings: on the whole data set, on random partitionings of the data set into two subsets of equal size, on the clinical grouping, and on the image-based clustering as determined by iCluster.&lt;br /&gt;
&lt;br /&gt;
[[Image:Two_templates_shenton50.png|center|600px|Two templates in a 50 subject MRI.]]&lt;br /&gt;
&lt;br /&gt;
We spatially normalized all the subjects into \textit{a standard space} using the iCluster algorithm with one-template and a 32x32x32 B-spline transformation model, and explored the alignment of the manual labels for clinical and image-based groupings. For each region of interest, such as amygdala, we computed the modified Haussdorff distance (MHD) in the standard space. MHD is a non -symmetric distance measure between the boundaries of two labels and is zero for perfect alignment.The MHD values for each region of interest were then summed up to obtain a total label distance for each ordered subject pair.&lt;br /&gt;
The following figure shows the total label distance for all subject pairings under the different groupings. We note that image-based clustering of iCluster (both with two-template and three-template)&lt;br /&gt;
groups subjects that have better label alignment, whereas the clinical grouping demonstrates no such coherence.&lt;br /&gt;
&lt;br /&gt;
[[Image:LabelAlignmentMatrixShenton50.png|center|600px|Label Alignment Matrices for the three groupings in the Shenton50 data set.]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
'''Experiment 2: Age groups in the OASIS data set'''&lt;br /&gt;
&lt;br /&gt;
In this experiment, we used the OASIS data set [http://www.oasis-brains.org] which consists of 416 pre-processed (skull stripped and gain-field corrected) brain MR images of subjects aged 18-96 years including individuals with early-stage Alzheimer's disease (AD). We ran iCluster on the whole data set while varying the number of templates from 2 through 6. Each run took approximately 4-8&lt;br /&gt;
hours on a 16 processor PC with 128GB RAM. For two- and three templates the algorithm computed unique and structurally different templates. We observed that these templates were robust: they were the same for random subsets of the data set of as little as 60 subjects. For larger number of templates, however, we observed that the computed templates were not all unique, or corresponded to single outlier subjects, or were not robust to random sub-sampling of the data set.&lt;br /&gt;
&lt;br /&gt;
The following figure shows the three robust templates computed by iCluster.&lt;br /&gt;
&lt;br /&gt;
[[Image:Three_templates_oasis.png|center|600px|Three templates of the OASIS data.]]&lt;br /&gt;
&lt;br /&gt;
The following figure shows the difference images between the three templates shown above.&lt;br /&gt;
&lt;br /&gt;
Difference_templates_oasis.png&lt;br /&gt;
&lt;br /&gt;
[[Image:Difference_templates_oasis.png|center|600px|Difference between the three templates of the OASIS data]]&lt;br /&gt;
 &lt;br /&gt;
The following figure includes the age distributions estimated using Parzen windowing with a Gaussian kernel and a s.t.d. of 4 years for each cluster identified by the algorithm.&lt;br /&gt;
&lt;br /&gt;
[[Image:Age_distributions_oasis.png|center|600px|Age groups in the OASIS data]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
'''Software'''&lt;br /&gt;
&lt;br /&gt;
The algorithm is currently implemented in the Insight ToolKit (ITK) and will be made publicly available. We also plan to integrate it into Slicer.&lt;br /&gt;
&lt;br /&gt;
= Key Investigators =&lt;br /&gt;
&lt;br /&gt;
MIT Algorithms: Mert R. Sabuncu and Polina Golland&lt;br /&gt;
&lt;br /&gt;
Harvard DBP 2: M.E. Shenton, M. Kubicki and S. Bouix&lt;br /&gt;
&lt;br /&gt;
= Publications =&lt;br /&gt;
''New''&lt;br /&gt;
&lt;br /&gt;
Discovering the Modes of an Image Population through Mixture Modeling, Mert R Sabuncu, Serdar Balci, and Polina Golland. Accepted to MICCAI '08.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''In Print''&lt;br /&gt;
&lt;br /&gt;
* [http://www.na-mic.org/pages/Special:Publications?text=multimodal+sabuncu&amp;amp;sub&lt;br /&gt;
mit=Search&amp;amp;words=all&amp;amp;title=checked&amp;amp;keywords=checked&amp;amp;authors=checked&amp;amp;abstract&lt;br /&gt;
=checked&amp;amp;sponsors=checked&amp;amp;searchbytag=checked| NA-MIC Publications Database]&lt;br /&gt;
&lt;br /&gt;
[[Category: Registration]]&lt;/div&gt;</summary>
		<author><name>Msabuncu</name></author>
		
	</entry>
</feed>