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	<entry>
		<id>https://www.na-mic.org/w/index.php?title=2008_Summer_Project_Week:fMRIconnectivity&amp;diff=27759</id>
		<title>2008 Summer Project Week:fMRIconnectivity</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=2008_Summer_Project_Week:fMRIconnectivity&amp;diff=27759"/>
		<updated>2008-06-27T14:15:15Z</updated>

		<summary type="html">&lt;p&gt;Ybkim: /* Key Investigators */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{|&lt;br /&gt;
|[[Image:ProjectWeek-2008.png|thumb|320px|Return to [[2008_Summer_Project_Week|Project Week Main Page]] ]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
__NOTOC__&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===Key Investigators===&lt;br /&gt;
* MIT: Bryce Kim, Polina Golland&lt;br /&gt;
* BWH: Jungsu Oh, Marek Kubicki&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;margin: 20px;&amp;quot;&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 27%; float: left; padding-right: 3%;&amp;quot;&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;h1&amp;gt;Objective&amp;lt;/h1&amp;gt;&lt;br /&gt;
Our objective is to study functional connectivity of schizophrenia patients versus normal with unsupervised data-driven analysis methods, such as ICA and clustering.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 27%; float: left; padding-right: 3%;&amp;quot;&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;h1&amp;gt;Approach, Plan&amp;lt;/h1&amp;gt;&lt;br /&gt;
&lt;br /&gt;
Our approach for investigating functional connectivity of schizophrenia patients is to apply probabilistic independent component analysis (PICA) and clustering based on Gaussian mixture model (GMM).&lt;br /&gt;
&lt;br /&gt;
Our plan for the project week is to first run such data-driven analysis methods on the data and then perform group analysis. We will also compare the results between PICA and GMM and investigate the factors that contribute to the differences. &lt;br /&gt;
&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 40%; float: left;&amp;quot;&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;h1&amp;gt;Progress&amp;lt;/h1&amp;gt;&lt;br /&gt;
&lt;br /&gt;
We have applied standard fMRI preprocessing steps on the data and regressed out the effects of white matter and ventricles. We have also customized PICA and GMM tools for our analysis purpose and obtained some preliminary results. &lt;br /&gt;
&lt;br /&gt;
During the project week, we completed applying PICA to both individual subjects and group analysis. We plan to discuss the results with the clinicians soon.&lt;br /&gt;
&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;br style=&amp;quot;clear: both;&amp;quot; /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
===References===&lt;br /&gt;
* C. Beckmann and S. Smith. &amp;quot;Probabilistic independent component analysis for functional magnetic resonance imaging.&amp;quot; IEEE Transactions on Medical Imaging, 23(2):137–152, 2004.&lt;/div&gt;</summary>
		<author><name>Ybkim</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=2008_Summer_Project_Week:fMRIconnectivity&amp;diff=26638</id>
		<title>2008 Summer Project Week:fMRIconnectivity</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=2008_Summer_Project_Week:fMRIconnectivity&amp;diff=26638"/>
		<updated>2008-06-10T20:06:39Z</updated>

		<summary type="html">&lt;p&gt;Ybkim: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{|&lt;br /&gt;
|[[Image:ProjectWeek-2008.png|thumb|320px|Return to [[2008_Summer_Project_Week|Project Week Main Page]] ]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
__NOTOC__&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===Key Investigators===&lt;br /&gt;
* MIT: Bryce Kim, Polina Golland&lt;br /&gt;
* BWH: Jungsu Oh, Marek Kubicki&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;margin: 20px;&amp;quot;&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 27%; float: left; padding-right: 3%;&amp;quot;&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;h1&amp;gt;Objective&amp;lt;/h1&amp;gt;&lt;br /&gt;
Our objective is to study functional connectivity of schizophrenia patients versus normal with unsupervised data-driven analysis methods, such as ICA and clustering.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 27%; float: left; padding-right: 3%;&amp;quot;&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;h1&amp;gt;Approach, Plan&amp;lt;/h1&amp;gt;&lt;br /&gt;
&lt;br /&gt;
Our approach for investigating functional connectivity of schizophrenia patients is to apply probabilistic independent component analysis (PICA) and clustering based on Gaussian mixture model (GMM).&lt;br /&gt;
&lt;br /&gt;
Our plan for the project week is to first run such data-driven analysis methods on the data and then perform group analysis. We will also compare the results between PICA and GMM and investigate the factors that contribute to the differences. &lt;br /&gt;
&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 40%; float: left;&amp;quot;&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;h1&amp;gt;Progress&amp;lt;/h1&amp;gt;&lt;br /&gt;
&lt;br /&gt;
We have applied standard fMRI preprocessing steps on the data and regressed out the effects of white matter and ventricles. We have also customized PICA and GMM tools for our analysis purpose and obtained some preliminary results. &lt;br /&gt;
&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;br style=&amp;quot;clear: both;&amp;quot; /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===References===&lt;br /&gt;
* C. Beckmann and S. Smith. &amp;quot;Probabilistic independent component analysis for functional magnetic resonance imaging.&amp;quot; IEEE Transactions on Medical Imaging, 23(2):137–152, 2004.&lt;/div&gt;</summary>
		<author><name>Ybkim</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=2008_Summer_Project_Week:fMRIconnectivity&amp;diff=26637</id>
		<title>2008 Summer Project Week:fMRIconnectivity</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=2008_Summer_Project_Week:fMRIconnectivity&amp;diff=26637"/>
		<updated>2008-06-10T20:03:47Z</updated>

		<summary type="html">&lt;p&gt;Ybkim: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{|&lt;br /&gt;
|[[Image:ProjectWeek-2008.png|thumb|320px|Return to [[2008_Summer_Project_Week|Project Week Main Page]] ]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
__NOTOC__&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===Key Investigators===&lt;br /&gt;
* MIT: Bryce Kim, Polina Golland&lt;br /&gt;
* BWH: Jungsu Oh, Marek Kubicki&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;margin: 20px;&amp;quot;&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 27%; float: left; padding-right: 3%;&amp;quot;&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;h1&amp;gt;Objective&amp;lt;/h1&amp;gt;&lt;br /&gt;
Our objective is to study functional connectivity of schizophrenia patients versus normal with unsupervised data-driven analysis methods, such as ICA and clustering.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 27%; float: left; padding-right: 3%;&amp;quot;&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;h1&amp;gt;Approach, Plan&amp;lt;/h1&amp;gt;&lt;br /&gt;
&lt;br /&gt;
Our approach for investigating functional connectivity of schizophrenia patients is to apply probabilistic independent component analysis (PICA) and clustering based on Gaussian mixture model (GMM).&lt;br /&gt;
&lt;br /&gt;
Our plan for the project week is to first run such data-driven analysis methods on the data and then perform group analysis. We will also compare the results between PICA and GMM and investigate the factors that contribute to the differences. &lt;br /&gt;
&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 40%; float: left;&amp;quot;&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;h1&amp;gt;Progress&amp;lt;/h1&amp;gt;&lt;br /&gt;
&lt;br /&gt;
We have applied standard fMRI preprocessing steps on the data and regressed out the effects of white matter and ventricles. We have also customized PICA for our analysis purpose and written GMM tools. &lt;br /&gt;
&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;br style=&amp;quot;clear: both;&amp;quot; /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===References===&lt;br /&gt;
* Fletcher, P.T., Tao, R., Jeong, W.-K., Whitaker, R.T., &amp;quot;A Volumetric Approach to Quantifying Region-to-Region White Matter Connectivity in Diffusion Tensor MRI,&amp;quot; to appear Information Processing in Medical Imaging (IPMI) 2007.&lt;/div&gt;</summary>
		<author><name>Ybkim</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=2008_Summer_Project_Week:fMRIconnectivity&amp;diff=26636</id>
		<title>2008 Summer Project Week:fMRIconnectivity</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=2008_Summer_Project_Week:fMRIconnectivity&amp;diff=26636"/>
		<updated>2008-06-10T19:43:39Z</updated>

		<summary type="html">&lt;p&gt;Ybkim: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{|&lt;br /&gt;
|[[Image:ProjectWeek-2008.png|thumb|320px|Return to [[2008_Summer_Project_Week|Project Week Main Page]] ]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
__NOTOC__&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===Key Investigators===&lt;br /&gt;
* MIT: Bryce Kim, Polina Golland&lt;br /&gt;
* BWH: Jungsu Oh, Marek Kubicki&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;margin: 20px;&amp;quot;&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 27%; float: left; padding-right: 3%;&amp;quot;&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;h1&amp;gt;Objective&amp;lt;/h1&amp;gt;&lt;br /&gt;
We are developing methods for analyzing diffusion tensor data along fiber tracts. The goal is to be able to make statistical group comparisons with fiber tracts as a common reference frame for comparison.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 27%; float: left; padding-right: 3%;&amp;quot;&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;h1&amp;gt;Approach, Plan&amp;lt;/h1&amp;gt;&lt;br /&gt;
&lt;br /&gt;
Our approach for analyzing diffusion tensors is summarized in the IPMI 2007 reference below.  The main challenge to this approach is &amp;lt;foo&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
Our plan for the project week is to first try out &amp;lt;bar&amp;gt;,...&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 40%; float: left;&amp;quot;&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;h1&amp;gt;Progress&amp;lt;/h1&amp;gt;&lt;br /&gt;
&lt;br /&gt;
Software for the fiber tracking and statistical analysis along the tracts has been implemented. The statistical methods for diffusion tensors are implemented as ITK code as part of the [[NA-MIC/Projects/Diffusion_Image_Analysis/DTI_Software_and_Algorithm_Infrastructure|DTI Software Infrastructure]] project. The methods have been validated on a repeated scan of a healthy individual. This work has been published as a conference paper (MICCAI 2005) and a journal version (MEDIA 2006). Our recent IPMI 2007 paper includes a nonparametric regression method for analyzing data along a fiber tract.&lt;br /&gt;
&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;br style=&amp;quot;clear: both;&amp;quot; /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===References===&lt;br /&gt;
* Fletcher, P.T., Tao, R., Jeong, W.-K., Whitaker, R.T., &amp;quot;A Volumetric Approach to Quantifying Region-to-Region White Matter Connectivity in Diffusion Tensor MRI,&amp;quot; to appear Information Processing in Medical Imaging (IPMI) 2007.&lt;br /&gt;
* C. Goodlett, I. Corouge, M. Jomier, and G. Gerig, A Quantitative DTI Fiber Tract Analysis Suite, The Insight Journal, vol. ISC/NAMIC/ MICCAI Workshop on Open-Source Software, 2005, Online publication: http://hdl.handle.net/1926/39 .&lt;/div&gt;</summary>
		<author><name>Ybkim</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=2008_Summer_Project_Week:fMRIconnectivity&amp;diff=26632</id>
		<title>2008 Summer Project Week:fMRIconnectivity</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=2008_Summer_Project_Week:fMRIconnectivity&amp;diff=26632"/>
		<updated>2008-06-10T19:30:26Z</updated>

		<summary type="html">&lt;p&gt;Ybkim: New page: ===Key Investigators=== * UNC: Isabelle Corouge, Casey Goodlett, Guido Gerig * Utah: Tom Fletcher, Ross Whitaker   &amp;lt;div style=&amp;quot;margin: 20px;&amp;quot;&amp;gt;  &amp;lt;div style=&amp;quot;width: 27%; float: left; padding...&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;===Key Investigators===&lt;br /&gt;
* UNC: Isabelle Corouge, Casey Goodlett, Guido Gerig&lt;br /&gt;
* Utah: Tom Fletcher, Ross Whitaker&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;margin: 20px;&amp;quot;&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 27%; float: left; padding-right: 3%;&amp;quot;&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;h1&amp;gt;Objective&amp;lt;/h1&amp;gt;&lt;br /&gt;
We are developing methods for analyzing diffusion tensor data along fiber tracts. The goal is to be able to make statistical group comparisons with fiber tracts as a common reference frame for comparison.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 27%; float: left; padding-right: 3%;&amp;quot;&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;h1&amp;gt;Approach, Plan&amp;lt;/h1&amp;gt;&lt;br /&gt;
&lt;br /&gt;
Our approach for analyzing diffusion tensors is summarized in the IPMI 2007 reference below.  The main challenge to this approach is &amp;lt;foo&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
Our plan for the project week is to first try out &amp;lt;bar&amp;gt;,...&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 40%; float: left;&amp;quot;&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;h1&amp;gt;Progress&amp;lt;/h1&amp;gt;&lt;br /&gt;
&lt;br /&gt;
Software for the fiber tracking and statistical analysis along the tracts has been implemented. The statistical methods for diffusion tensors are implemented as ITK code as part of the [[NA-MIC/Projects/Diffusion_Image_Analysis/DTI_Software_and_Algorithm_Infrastructure|DTI Software Infrastructure]] project. The methods have been validated on a repeated scan of a healthy individual. This work has been published as a conference paper (MICCAI 2005) and a journal version (MEDIA 2006). Our recent IPMI 2007 paper includes a nonparametric regression method for analyzing data along a fiber tract.&lt;br /&gt;
&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;br style=&amp;quot;clear: both;&amp;quot; /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;/div&gt;</summary>
		<author><name>Ybkim</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=2008_Summer_Project_Week&amp;diff=26631</id>
		<title>2008 Summer Project Week</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=2008_Summer_Project_Week&amp;diff=26631"/>
		<updated>2008-06-10T19:29:22Z</updated>

		<summary type="html">&lt;p&gt;Ybkim: /* Other Projects */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Back to [[Engineering:Programming_Events|Programming/Project Events]]&lt;br /&gt;
&lt;br /&gt;
[[Image:ProjectWeek-2008.png|thumb|220px|right|Summer 2008]]&lt;br /&gt;
&lt;br /&gt;
== Logistics ==&lt;br /&gt;
&lt;br /&gt;
'''Dates:''' June 23-27, 2008&lt;br /&gt;
&lt;br /&gt;
'''Location:''' MIT. [[Meeting_Locations:MIT_Grier_A_%26B|Grier Rooms A &amp;amp; B: 34-401A &amp;amp; 34-401B]].&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
'''Registration Fee:''' $260 (this will cover the cost of breakfast, lunch and coffee breaks for the week). Due by Friday, June 13th, 2008. Please make checks out to &amp;quot;Massachusetts Institute of Technology&amp;quot; and mail to: Donna Kaufman, MIT, 77 Massachusetts Ave., 38-409a, Cambridge, MA 02139&lt;br /&gt;
&lt;br /&gt;
'''Registration Method''' Please add your name to the attendee list below (create namic wiki account if you don't have one, by clicking on the &amp;quot;login/create account&amp;quot; link on the top right corner of this page), and then mail a check to Donna Kaufman at the address above.&lt;br /&gt;
&lt;br /&gt;
If you are attending for one day only, the registration fee is not required.&lt;br /&gt;
&lt;br /&gt;
'''Hotel:''' We have a group rate of $239/night (plus tax) for a room with either 1 king or 2 queen beds at the [http://www.hotelatmit.com Hotel at MIT (now called Le Meridien)]. [http://www.starwoodmeeting.com/StarGroupsWeb/booking/reservation?id=0805167317&amp;amp;key=4FD1B  Please click here to reserve.]This rate is good only through June 1.&lt;br /&gt;
&lt;br /&gt;
Here is some information about several other Boston area hotels that are convenient to NA-MIC events: [[Boston_Hotels|Boston_Hotels]]. Summer is tourist season in Boston, so please book your rooms early.&lt;br /&gt;
&lt;br /&gt;
([[Project Week Logistics Checklist|This is a checklist for the onsite planning items]])&lt;br /&gt;
&lt;br /&gt;
==Introduction to NA-MIC Project Week==&lt;br /&gt;
&lt;br /&gt;
NA-MIC Project Week is a hands on activity -- programming using the [[NA-MIC-Kit|NA-MIC Kit]], algorithm design, and clinical application -- that has become one of the major events in the [[NA-MIC-Kit|NA-MIC Kit]] calendar. This event is the seventh of the [[Engineering:Programming_Events|'''series''']]. It is held in the summer at MIT (typically the last week of June), and a shorter version is held in Salt Lake City in the winter (typically the second week of January).  &lt;br /&gt;
The main goal of these events if to move forward the deliverables of NA-MIC. NA-MIC participants and their collaborators are welcome to attend.  &lt;br /&gt;
&lt;br /&gt;
* NA-MIC Members: Participation in this event is voluntary -- if you don't think this will help you move forward in your work, there is no obligation to attend.&lt;br /&gt;
* Ideal candidates are those who want to contribute to the [[NA-MIC-Kit|NA-MIC Kit]], and those who can help make it happen.&lt;br /&gt;
* This is not an introduction to the components of the [[NA-MIC-Kit|NA-MIC Kit]].&lt;br /&gt;
* NA-MIC Core 1 (Algorithms) - bring your algorithms and code to work on in the company of Core 2 engineers and Core 3 scientists.&lt;br /&gt;
* NA-MIC Core 2 (Engineering) - bring your code for infrastructure and applications to extend the [[NA-MIC-Kit|NA-MIC Kit]] capabilities, integrate Core 1 algorithms, and refine workflows for Core 3.&lt;br /&gt;
* NA-MIC Core 3 (DBP) - bring your data to work on with the [[NA-MIC-Kit|NA-MIC Kit]] and get assistance and provide feedback to Core 1 scientists and Core 2 engineers.&lt;br /&gt;
* External Collaborators - if you are working on a project that uses the [[NA-MIC-Kit|NA-MIC kit]], and want to participate to get help from NA-MIC Engineering, please send an email to Tina Kapur (tkapur at bwh.harvard.edu).  Please note that the event is open to people outside NA-MIC, subject to availability.&lt;br /&gt;
* Everyone should '''bring a laptop'''. We will have four projectors.&lt;br /&gt;
* About half the time will be spent working on projects and the other half in project related discussions.&lt;br /&gt;
* You '''do''' need to be actively working on a NA-MIC related project in order to make this investment worthwhile for everyone.&lt;br /&gt;
&lt;br /&gt;
== Agenda==&lt;br /&gt;
* Monday &lt;br /&gt;
** noon-1pm lunch &lt;br /&gt;
**1pm: Welcome (Ron Kikinis)&lt;br /&gt;
** 1:05-3:30pm Introduce [[#Projects|Projects]] using templated wiki pages (all Project Leads) ([[NA-MIC/Projects/Theme/Template|Wiki Template]]) &lt;br /&gt;
** 3:30-5:30pm Start project work&lt;br /&gt;
* Tuesday &lt;br /&gt;
** 8:30am breakfast&lt;br /&gt;
** 9:00-9:45am: NA-MIC Software Process &lt;br /&gt;
** 10-10:30am [[Project Week 2008 Slicer 3.0 Update|Slicer 3.0 Update]] (Jim Miller, Steve Pieper)&lt;br /&gt;
** noon lunch&lt;br /&gt;
** 2:30-3:30pm: [[Project Week 2008 Special topic breakout: Non-Linear Registration]] &lt;br /&gt;
** 5:30pm adjourn for day&lt;br /&gt;
* Wednesday &lt;br /&gt;
** 8:30am breakfast&lt;br /&gt;
** 9:00-12pm [[Project Week 2008 Special topic breakout: ITK]] (Luis Ibanez)&lt;br /&gt;
** noon lunch&lt;br /&gt;
** 2:30-3:30pm: [[Project Week 2008 Special topic breakout: XNAT Database]] (Daniel Marcus)&lt;br /&gt;
** 5:30pm adjourn for day&lt;br /&gt;
* Thursday&lt;br /&gt;
** 8:30am breakfast&lt;br /&gt;
** noon lunch&lt;br /&gt;
**2:30-3:30pm [[Project Week 2008 Special topic breakout: GWE]] (Marco Ruiz)&lt;br /&gt;
** 5:30pm adjourn for day&lt;br /&gt;
* Friday &lt;br /&gt;
** 8:30am breakfast&lt;br /&gt;
** 10am-noon: Project Progress using update [[#Projects|Project Wiki pages]]&lt;br /&gt;
** noon lunch boxes and adjourn.  (Next one [[AHM_2009| in Utah the week of Jan 5, 2009]])&lt;br /&gt;
&lt;br /&gt;
== Preparation ==&lt;br /&gt;
&lt;br /&gt;
# Please make sure that you are on the http://public.kitware.com/cgi-bin/mailman/listinfo/na-mic-project-week mailing list&lt;br /&gt;
&lt;br /&gt;
# [[Engineering:TCON_2008|May 08 and May 15 TCON DBPs ONLY]] at 3pm ET to discuss NA-MIC DBP Projects ONLY. &lt;br /&gt;
# [[Engineering:TCON_2008|May 22 TCON#1]] at 3pm ET to discuss NA-MIC Engr Core Projects and Assign/Verify Teams&lt;br /&gt;
# [[Engineering:TCON_2008|May 29 TCON#2]] at 3pm ET to discuss NA-MIC ALGORITHMS Core Lead Projects.  Project leads should sign up for a slot [[Engineering:TCON_2008|here]]. Projects will be discussed in order of the signups. &lt;br /&gt;
# [[Engineering:TCON_2008|June 5 TCON#3]] at 3pm ET to discuss NA-MIC EXTERNAL Collaborations.  All NIH funded &amp;quot;collaborations with NCBC&amp;quot; leads should call. Project leads should sign up for a slot [[Engineering:TCON_2008|here]].  Projects will be discussed in order of the signups. &lt;br /&gt;
# [[Engineering:TCON_2008|June 12 TCON#4]] at 3pm ET to discuss NA-MIC EXTERNAL Collaborations.  All other collaboration leads should call. Project leads should sign up for a slot [[Engineering:TCON_2008|here]].  Projects will be discussed in order of the signups. &lt;br /&gt;
# [[Engineering:TCON_2008|June 19 TCON#5]] at 3pm ET to tie loose ends.  Anyone with un-addressed questions should call.&lt;br /&gt;
# By 3pm ET on June 12, 2008: [[NA-MIC/Projects/Theme/Template|Complete a templated wiki page for your project]]. Please do not edit the template page itself, but create a new page for your project and cut-and-paste the text from this template page.  If you have questions, please send an email to tkapur at bwh.harvard.edu.&lt;br /&gt;
# By 3pm on June 19, 2008: Create a directory for each project on the [[Engineering:SandBox|NAMIC Sandbox]] (Zack)&lt;br /&gt;
## Commit on each sandbox directory the code examples/snippets that represent our first guesses of appropriate methods. (Luis and Steve will help with this, as needed)&lt;br /&gt;
## Gather test images in any of the Data sharing resources we have (e.g. the BIRN). These ones don't have to be many. At least three different cases, so we can get an idea of the modality-specific characteristics of these images. Put the IDs of these data sets on the wiki page. (the participants must do this.)&lt;br /&gt;
## Setup nightly tests on a separate Dashboard, where we will run the methods that we are experimenting with. The test should post result images and computation time. (Zack)&lt;br /&gt;
# Please note that by the time we get to the project event, we should be trying to close off a project milestone rather than starting to work on one...&lt;br /&gt;
&lt;br /&gt;
== A History in Wiki Links ==&lt;br /&gt;
&lt;br /&gt;
A history of all the programming/project events in NA-MIC is available by following [[Engineering:Programming_Events|this link]].&lt;br /&gt;
&lt;br /&gt;
== Projects ==&lt;br /&gt;
&lt;br /&gt;
===DBP II===&lt;br /&gt;
These are projects by the new set of DBPS:&lt;br /&gt;
#[[DBP2:Harvard|Velocardio Facial Syndrome (VCFS) as a Genetic Model for Schizophrenia]] (Harvard: Marek Kubicki, PI)&lt;br /&gt;
##EPI-DWI Distortion correction (Sylvain Bouix BWH, Tauseef Rehman GATech)&lt;br /&gt;
##[[2008_Summer_Project_Week:EddyCurrentCorrection|EPI-DWI Eddy Current distortion correction]] (Sylvain Bouix BWH, Ran Tao Utah)&lt;br /&gt;
##Lobe Parcellation of 3T MR data - need help parametrization (Sylvain Bouix BWH, Priya Srinivasan BWH, Brad Davis Kitware)&lt;br /&gt;
##Finsler method (John Melonakos GATech, Marek Kubicki BWH)&lt;br /&gt;
##Group Analysis on DTI (Casey Goodlett Utah, Marek Kubicki BWH)&lt;br /&gt;
#[[DBP2:UNC|Longitudinal MRI Study of Early Brain Development in Autism]] (UNC: Heather Hazlett, Joseph Piven, PI)&lt;br /&gt;
##Work Flow Tool for regional cortical thickness pipeline (Clement Vachet UNC)&lt;br /&gt;
##NITRC registration of cortical thickness modules (Clement Vachet UNC)&lt;br /&gt;
##DTI tools for a) DWI preparation and b) DTI atlas building (Zhexing Liu UNC) &lt;br /&gt;
#[[DBP2:MIND|Analysis of Brain Lesions in Lupus]] (MIND/UNM: Jeremy Bockholt, Charles Gasparovic PI)&lt;br /&gt;
##[[DBP2:MIND:RoadmapProject|Finish Roadmap Project]]&lt;br /&gt;
##[[DBP2:MIND:LongitudinalRegistrationProject|Longitudinal Registration]]&lt;br /&gt;
##[[DBP2:MIND:BeyondLesionsProject|Beyond Lesions]]&lt;br /&gt;
#[[DBP2:JHU|Segmentation and Registration Tools for Robotic Prostate Intervention]] (Queens/JHU: Gabor Fichtinger, PI)&lt;br /&gt;
##[[DBP2:JHU:Roadmap|Trans-Rectal Prostate Biopsy module (David Gobbi, Gabor Fichtinger, Queens/JHU)]]&lt;br /&gt;
##[[Projects:ProstateSegmentation|Prostate Segmentation and Registration (Yi Gao GATech, Gabor Fichtinger JHU)]]&lt;br /&gt;
##Hardware/software overlay for percutaneous intervention (Siddharth Vikal, Gabor Fichtinger, Queens/JHU)&lt;br /&gt;
&lt;br /&gt;
===Other Projects===&lt;br /&gt;
#[[2008_Summer_Project_Week:EddyCurrentCorrection|Eddy current and head motion correction of DWIs]] (Ran Tao, Utah, Sylvain Bouix, BWH, Xiaodong Tao, GE, Tom Fletcher, Utah)&lt;br /&gt;
#Integraton of groupwise b-spline registration into atlas building (Casey Goodlett, Serdar Balci)&lt;br /&gt;
# CVS / SVN auto synchronization&lt;br /&gt;
# 3D Widgets in Slicer&lt;br /&gt;
## Issues with existing widgets&lt;br /&gt;
## Design of new widgets&lt;br /&gt;
# Batch processing in the NAMIC Kit (Julien, Marco, Steve, Jim)&lt;br /&gt;
# Module Chaining (Marco, Jim, Steve, Dan B., Luca)&lt;br /&gt;
# Nonlinear transforms (Jim, Steve, Luis)&lt;br /&gt;
## TransformToWorld/TransformFromWorld, integration with slice viewing&lt;br /&gt;
# Slicer3, XNAT integration, and desigining XCEDE Web Services (Dan M., Steve, Julien, Dan B.)&lt;br /&gt;
## Review and enrich use cases&lt;br /&gt;
# Python in Slicer (Dan B., Michael Halle, Steve, Luca)&lt;br /&gt;
# Performance Tuning of Fiducials using the EventBroker and other tools (Nicole, Alex, Steve, Will)&lt;br /&gt;
# GUI Tweaking (Wendy, Sebastien) [http://www.na-mic.org/Bug/view.php?id=242]&lt;br /&gt;
# [[2008_Summer_Project_Week:fMRIconnectivity|fMRI connectivity]]  (Bryce Kim, MIT)&lt;br /&gt;
&lt;br /&gt;
===External Collaborations===&lt;br /&gt;
#[[NA-MIC/Projects/Collaboration/UWA-Perth]] (Adam Wittek)&lt;br /&gt;
#[[NA-MIC/Projects/Collaboration/MRSI Module for Slicer]] (Bjoern Menze)&lt;br /&gt;
#[[NA-MIC/Projects/Collaboration/NIREP: Non-rigid Image Registration Evaluation]] (Gary Christensen Group)&lt;br /&gt;
#[[NA-MIC/Projects/Collaboration/Lung Atlas]] (Gary Christensen Group)&lt;br /&gt;
#Non-rigid image registration (Gary Christensen Group)&lt;br /&gt;
#[[NA-MIC/Projects/Collaboration/SARP phantom]] (Keith Gunderson)&lt;br /&gt;
#FMA (Protege) links to Slicer (Vish, Mike, Florin, Jim, Steve, Wendy)&lt;br /&gt;
#[[NA-MIC/Projects/External Collaboration/Measuring Alcohol and Stress Interaction]]&lt;br /&gt;
#[[NA-MIC/Projects/External Collaboration/Slicer3-vmtk Integration]] (Luca Antiga)&lt;br /&gt;
#[[NA-MIC/Projects/External Collaboration/Mesh Generation Summer 2008]] (Iowa Group)&lt;br /&gt;
&lt;br /&gt;
===Non-Medical Collaborations===&lt;br /&gt;
#[[NA-MIC/Projects/Non-Medical Collaborations/Astronomical Medicine|Astronomical Medicine]] (Harvard IIC: Douglas Alan, Michael Halle)&lt;br /&gt;
&lt;br /&gt;
==Attendee List==&lt;br /&gt;
# Ron Kikinis, BWH&lt;br /&gt;
# Carl-Fredrik Westin, BWH&lt;br /&gt;
# Gary Christensen, The University of Iowa&lt;br /&gt;
# Jeffrey Hawley, Gary Christensen's student&lt;br /&gt;
# Kate Raising, Gary Christensen's student&lt;br /&gt;
# Nathan Fritze, Gary Christensen's student&lt;br /&gt;
# Paul Song, Gary Christensen's student&lt;br /&gt;
# Cheng Zhang, Gary Christensen's student&lt;br /&gt;
# Ying Wei, Gary Christensen's student&lt;br /&gt;
# Nathan Burnette, The University of Iowa&lt;br /&gt;
# Hans Johnson, The University of Iowa&lt;br /&gt;
# Vincent Magnotta, The University of Iowa&lt;br /&gt;
# Keith Gunderson, The University of Iowa&lt;br /&gt;
# Steve Pieper, Isomics, Core 2/6&lt;br /&gt;
# Dana C. Peters, BIDMC Harvard Medical&lt;br /&gt;
# Jason Taclas, BIDMC Harvard Medical&lt;br /&gt;
# Nicole Aucoin, BWH, Core 2&lt;br /&gt;
# Will Schroeder, Kitware, Cores 2/4&lt;br /&gt;
# Sebastien Barre, Kitware, Core 2&lt;br /&gt;
# Julien Jomier, Kitware, Core 2&lt;br /&gt;
# Luis Ibanez, Kitware, Core 2&lt;br /&gt;
# Curtis Lisle, KnowledgeVis, Core 2&lt;br /&gt;
# Katie Hayes, BWH, Core 2&lt;br /&gt;
# Randy Gollub, MGH, Core 5&lt;br /&gt;
# Clement Vachet, UNC, Core 3&lt;br /&gt;
# Zhexing Liu, UNC, Core 1/3&lt;br /&gt;
# Casey Goodlett, Utah, Core 1&lt;br /&gt;
# Marcel Prastawa, Utah, Core 1&lt;br /&gt;
# Jeffrey Grethe, UCSD, Core 2&lt;br /&gt;
# Marco Ruiz, UCSD, Core 2&lt;br /&gt;
# Zhen Qian, Rutgers University&lt;br /&gt;
# Jinghao Zhou, Rutgers University&lt;br /&gt;
# Luca Antiga, Mario Negri Institute&lt;br /&gt;
# Adam Wittek, The University of Western Australia&lt;br /&gt;
# Grand Joldes, The University of Western Australia&lt;br /&gt;
# Jamie Berger, The University of Western Australia&lt;br /&gt;
# Serdar Balci, MIT, Core 1&lt;br /&gt;
# Bryce Kim, MIT, Core1&lt;br /&gt;
# Tina Kapur, BWH, Core 6&lt;br /&gt;
# Carling Cheung, Robarts Research Institute / The University of Western Ontario&lt;br /&gt;
# Danielle Pace, Robarts Research Institute / The University of Western Ontario&lt;br /&gt;
# Sean Megason, Dept of Systems Biology, Harvard Medical School&lt;br /&gt;
# Alex Gouaillard, Dept of Systems Biology, Harvard Medical School&lt;br /&gt;
# Kishore Mosaliganti, Dept of Systems Biology, Harvard Medical School&lt;br /&gt;
# Arnaud Gelas, Dept of Systems Biology, Harvard Medical School&lt;br /&gt;
# Sonia Pujol, Surgical Planning Laboratory, BWH&lt;br /&gt;
# Bjoern Menze, (then) Surgical Planning Laboratory, BWH&lt;br /&gt;
# Alex Yarmarkovich, Isomics, Core 2&lt;br /&gt;
# Sylvain Bouix, BWH, Core 3&lt;br /&gt;
# Priya Srinivasan, BWH, Core 3&lt;br /&gt;
# Chris Churas, UCSD, Core 2&lt;br /&gt;
# John Melonakos, Georgia Tech, Core 1&lt;br /&gt;
# Yi Gao, Georgia Tech, Core 1&lt;br /&gt;
# Tauseef Rehman, Georgia Tech, Core 1&lt;br /&gt;
# Clare Poynton, MIT, Core 1&lt;br /&gt;
# H. Jeremy Bockholt, MRN Lupus DBP Core 3&lt;br /&gt;
# Mark Scully, MRN Lupus DBP Core 3&lt;br /&gt;
# Gabor Fichtinger, Queen's, Core 3&lt;br /&gt;
# David Gobbi, Queen's, Core 3&lt;br /&gt;
# Purang Abolmaesumi, Queen's, Core 3&lt;br /&gt;
# Siddharth Vikal, Queen's, Core 3&lt;br /&gt;
# Daniel Blezek, Mayo&lt;br /&gt;
# Csaba Csoma, JHU, Core 3&lt;br /&gt;
# Ran Tao, University of Utah, Core 1&lt;br /&gt;
# Jim Miller, GE Research, Core 2&lt;br /&gt;
# Xiaodong Tao, GE Research, Core 2&lt;br /&gt;
# Dirk Padfield, GE Research, Core 2&lt;br /&gt;
# Viswanath Avasarala, GE Research, NAC&lt;br /&gt;
# Dan Marcus, Washington University   &lt;br /&gt;
# Tim Olsen, Washington University   &lt;br /&gt;
# Kevin Archie, Washington University   &lt;br /&gt;
# Misha Milchenko, Washington University&lt;br /&gt;
# Wendy Plesniak, BWH, Core 2&lt;br /&gt;
# Demian Wasserman, INRIA, LMI-collaborator&lt;br /&gt;
# Xenophon Papademetris, Yale, Collaborator&lt;br /&gt;
# Xenophon P's postdoc, Yale, Collaborator&lt;br /&gt;
# Xenophon P's student, Yale, Collaborator&lt;br /&gt;
# Vidya Rajagopalan, Virginia Tech, Student of Chris Wyatt, External Collaborator&lt;br /&gt;
# Greg Sharp, MGH, External Collaborator&lt;br /&gt;
# Marta Peroni, MGH, External Collaborator&lt;br /&gt;
# Toru Higaki, Hiroshima Univ., Japan, External collaborator (Hata)&lt;br /&gt;
# Jacek Kukluk, BWH,&lt;br /&gt;
# Nobuhiko Hata, BWH&lt;br /&gt;
# Junichi Tokuda, BWH&lt;br /&gt;
# Haying Liu, BWH&lt;br /&gt;
# Ragini Verma, UPenn (June 24)&lt;br /&gt;
# Luke Bloy, UPenn (Ragini Verma's student) (June 24)&lt;br /&gt;
# Yang Li, UPenn (Ragini's postdoc) (June 24)&lt;br /&gt;
# Jack Blevins, Acoustic Med, Collaborator&lt;br /&gt;
# Nikos Chrisochoides, College of William and Mary, External collaborator (June 23)&lt;br /&gt;
# Andriy Fedorov, College of William and Mary, External collaborator&lt;br /&gt;
# Carlos Sánchez Mendoza, BWH &lt;br /&gt;
# Kilian Pohl, BWH&lt;br /&gt;
# Pratik Patel, Brainlab, Collaborator&lt;br /&gt;
# Marianna Jakab, BWH&lt;br /&gt;
# Nathan Hageman, UCLA&lt;br /&gt;
# Douglas Alan, Harvard IIC, External Collaborator&lt;br /&gt;
# Tammy Riklin Raviv, MIT&lt;br /&gt;
# Peter Kazanzides, JHU, Collaborator&lt;br /&gt;
# Scott Hoge, BWH, (Wed, Jun 25)&lt;br /&gt;
#*WE HAVE REACHED CAPACITY. REGISTRATION IS CLOSED. [[User:Tkapur|Tkapur]] 19:42, 6 June 2008 (UTC)&lt;br /&gt;
&lt;br /&gt;
==Pictures==&lt;/div&gt;</summary>
		<author><name>Ybkim</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=2008_Summer_Project_Week&amp;diff=26628</id>
		<title>2008 Summer Project Week</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=2008_Summer_Project_Week&amp;diff=26628"/>
		<updated>2008-06-10T19:18:32Z</updated>

		<summary type="html">&lt;p&gt;Ybkim: /* Other Projects */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Back to [[Engineering:Programming_Events|Programming/Project Events]]&lt;br /&gt;
&lt;br /&gt;
[[Image:ProjectWeek-2008.png|thumb|220px|right|Summer 2008]]&lt;br /&gt;
&lt;br /&gt;
== Logistics ==&lt;br /&gt;
&lt;br /&gt;
'''Dates:''' June 23-27, 2008&lt;br /&gt;
&lt;br /&gt;
'''Location:''' MIT. [[Meeting_Locations:MIT_Grier_A_%26B|Grier Rooms A &amp;amp; B: 34-401A &amp;amp; 34-401B]].&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
'''Registration Fee:''' $260 (this will cover the cost of breakfast, lunch and coffee breaks for the week). Due by Friday, June 13th, 2008. Please make checks out to &amp;quot;Massachusetts Institute of Technology&amp;quot; and mail to: Donna Kaufman, MIT, 77 Massachusetts Ave., 38-409a, Cambridge, MA 02139&lt;br /&gt;
&lt;br /&gt;
'''Registration Method''' Please add your name to the attendee list below (create namic wiki account if you don't have one, by clicking on the &amp;quot;login/create account&amp;quot; link on the top right corner of this page), and then mail a check to Donna Kaufman at the address above.&lt;br /&gt;
&lt;br /&gt;
If you are attending for one day only, the registration fee is not required.&lt;br /&gt;
&lt;br /&gt;
'''Hotel:''' We have a group rate of $239/night (plus tax) for a room with either 1 king or 2 queen beds at the [http://www.hotelatmit.com Hotel at MIT (now called Le Meridien)]. [http://www.starwoodmeeting.com/StarGroupsWeb/booking/reservation?id=0805167317&amp;amp;key=4FD1B  Please click here to reserve.]This rate is good only through June 1.&lt;br /&gt;
&lt;br /&gt;
Here is some information about several other Boston area hotels that are convenient to NA-MIC events: [[Boston_Hotels|Boston_Hotels]]. Summer is tourist season in Boston, so please book your rooms early.&lt;br /&gt;
&lt;br /&gt;
([[Project Week Logistics Checklist|This is a checklist for the onsite planning items]])&lt;br /&gt;
&lt;br /&gt;
==Introduction to NA-MIC Project Week==&lt;br /&gt;
&lt;br /&gt;
NA-MIC Project Week is a hands on activity -- programming using the [[NA-MIC-Kit|NA-MIC Kit]], algorithm design, and clinical application -- that has become one of the major events in the [[NA-MIC-Kit|NA-MIC Kit]] calendar. This event is the seventh of the [[Engineering:Programming_Events|'''series''']]. It is held in the summer at MIT (typically the last week of June), and a shorter version is held in Salt Lake City in the winter (typically the second week of January).  &lt;br /&gt;
The main goal of these events if to move forward the deliverables of NA-MIC. NA-MIC participants and their collaborators are welcome to attend.  &lt;br /&gt;
&lt;br /&gt;
* NA-MIC Members: Participation in this event is voluntary -- if you don't think this will help you move forward in your work, there is no obligation to attend.&lt;br /&gt;
* Ideal candidates are those who want to contribute to the [[NA-MIC-Kit|NA-MIC Kit]], and those who can help make it happen.&lt;br /&gt;
* This is not an introduction to the components of the [[NA-MIC-Kit|NA-MIC Kit]].&lt;br /&gt;
* NA-MIC Core 1 (Algorithms) - bring your algorithms and code to work on in the company of Core 2 engineers and Core 3 scientists.&lt;br /&gt;
* NA-MIC Core 2 (Engineering) - bring your code for infrastructure and applications to extend the [[NA-MIC-Kit|NA-MIC Kit]] capabilities, integrate Core 1 algorithms, and refine workflows for Core 3.&lt;br /&gt;
* NA-MIC Core 3 (DBP) - bring your data to work on with the [[NA-MIC-Kit|NA-MIC Kit]] and get assistance and provide feedback to Core 1 scientists and Core 2 engineers.&lt;br /&gt;
* External Collaborators - if you are working on a project that uses the [[NA-MIC-Kit|NA-MIC kit]], and want to participate to get help from NA-MIC Engineering, please send an email to Tina Kapur (tkapur at bwh.harvard.edu).  Please note that the event is open to people outside NA-MIC, subject to availability.&lt;br /&gt;
* Everyone should '''bring a laptop'''. We will have four projectors.&lt;br /&gt;
* About half the time will be spent working on projects and the other half in project related discussions.&lt;br /&gt;
* You '''do''' need to be actively working on a NA-MIC related project in order to make this investment worthwhile for everyone.&lt;br /&gt;
&lt;br /&gt;
== Agenda==&lt;br /&gt;
* Monday &lt;br /&gt;
** noon-1pm lunch &lt;br /&gt;
**1pm: Welcome (Ron Kikinis)&lt;br /&gt;
** 1:05-3:30pm Introduce [[#Projects|Projects]] using templated wiki pages (all Project Leads) ([[NA-MIC/Projects/Theme/Template|Wiki Template]]) &lt;br /&gt;
** 3:30-5:30pm Start project work&lt;br /&gt;
* Tuesday &lt;br /&gt;
** 8:30am breakfast&lt;br /&gt;
** 9:00-9:45am: NA-MIC Software Process &lt;br /&gt;
** 10-10:30am [[Project Week 2008 Slicer 3.0 Update|Slicer 3.0 Update]] (Jim Miller, Steve Pieper)&lt;br /&gt;
** noon lunch&lt;br /&gt;
** 2:30-3:30pm: [[Project Week 2008 Special topic breakout: Non-Linear Registration]] &lt;br /&gt;
** 5:30pm adjourn for day&lt;br /&gt;
* Wednesday &lt;br /&gt;
** 8:30am breakfast&lt;br /&gt;
** 9:00-12pm [[Project Week 2008 Special topic breakout: ITK]] (Luis Ibanez)&lt;br /&gt;
** noon lunch&lt;br /&gt;
** 2:30-3:30pm: [[Project Week 2008 Special topic breakout: XNAT Database]] (Daniel Marcus)&lt;br /&gt;
** 5:30pm adjourn for day&lt;br /&gt;
* Thursday&lt;br /&gt;
** 8:30am breakfast&lt;br /&gt;
** noon lunch&lt;br /&gt;
**2:30-3:30pm [[Project Week 2008 Special topic breakout: GWE]] (Marco Ruiz)&lt;br /&gt;
** 5:30pm adjourn for day&lt;br /&gt;
* Friday &lt;br /&gt;
** 8:30am breakfast&lt;br /&gt;
** 10am-noon: Project Progress using update [[#Projects|Project Wiki pages]]&lt;br /&gt;
** noon lunch boxes and adjourn.  (Next one [[AHM_2009| in Utah the week of Jan 5, 2009]])&lt;br /&gt;
&lt;br /&gt;
== Preparation ==&lt;br /&gt;
&lt;br /&gt;
# Please make sure that you are on the http://public.kitware.com/cgi-bin/mailman/listinfo/na-mic-project-week mailing list&lt;br /&gt;
&lt;br /&gt;
# [[Engineering:TCON_2008|May 08 and May 15 TCON DBPs ONLY]] at 3pm ET to discuss NA-MIC DBP Projects ONLY. &lt;br /&gt;
# [[Engineering:TCON_2008|May 22 TCON#1]] at 3pm ET to discuss NA-MIC Engr Core Projects and Assign/Verify Teams&lt;br /&gt;
# [[Engineering:TCON_2008|May 29 TCON#2]] at 3pm ET to discuss NA-MIC ALGORITHMS Core Lead Projects.  Project leads should sign up for a slot [[Engineering:TCON_2008|here]]. Projects will be discussed in order of the signups. &lt;br /&gt;
# [[Engineering:TCON_2008|June 5 TCON#3]] at 3pm ET to discuss NA-MIC EXTERNAL Collaborations.  All NIH funded &amp;quot;collaborations with NCBC&amp;quot; leads should call. Project leads should sign up for a slot [[Engineering:TCON_2008|here]].  Projects will be discussed in order of the signups. &lt;br /&gt;
# [[Engineering:TCON_2008|June 12 TCON#4]] at 3pm ET to discuss NA-MIC EXTERNAL Collaborations.  All other collaboration leads should call. Project leads should sign up for a slot [[Engineering:TCON_2008|here]].  Projects will be discussed in order of the signups. &lt;br /&gt;
# [[Engineering:TCON_2008|June 19 TCON#5]] at 3pm ET to tie loose ends.  Anyone with un-addressed questions should call.&lt;br /&gt;
# By 3pm ET on June 12, 2008: [[NA-MIC/Projects/Theme/Template|Complete a templated wiki page for your project]]. Please do not edit the template page itself, but create a new page for your project and cut-and-paste the text from this template page.  If you have questions, please send an email to tkapur at bwh.harvard.edu.&lt;br /&gt;
# By 3pm on June 19, 2008: Create a directory for each project on the [[Engineering:SandBox|NAMIC Sandbox]] (Zack)&lt;br /&gt;
## Commit on each sandbox directory the code examples/snippets that represent our first guesses of appropriate methods. (Luis and Steve will help with this, as needed)&lt;br /&gt;
## Gather test images in any of the Data sharing resources we have (e.g. the BIRN). These ones don't have to be many. At least three different cases, so we can get an idea of the modality-specific characteristics of these images. Put the IDs of these data sets on the wiki page. (the participants must do this.)&lt;br /&gt;
## Setup nightly tests on a separate Dashboard, where we will run the methods that we are experimenting with. The test should post result images and computation time. (Zack)&lt;br /&gt;
# Please note that by the time we get to the project event, we should be trying to close off a project milestone rather than starting to work on one...&lt;br /&gt;
&lt;br /&gt;
== A History in Wiki Links ==&lt;br /&gt;
&lt;br /&gt;
A history of all the programming/project events in NA-MIC is available by following [[Engineering:Programming_Events|this link]].&lt;br /&gt;
&lt;br /&gt;
== Projects ==&lt;br /&gt;
&lt;br /&gt;
===DBP II===&lt;br /&gt;
These are projects by the new set of DBPS:&lt;br /&gt;
#[[DBP2:Harvard|Velocardio Facial Syndrome (VCFS) as a Genetic Model for Schizophrenia]] (Harvard: Marek Kubicki, PI)&lt;br /&gt;
##EPI-DWI Distortion correction (Sylvain Bouix BWH, Tauseef Rehman GATech)&lt;br /&gt;
##[[2008_Summer_Project_Week:EddyCurrentCorrection|EPI-DWI Eddy Current distortion correction]] (Sylvain Bouix BWH, Ran Tao Utah)&lt;br /&gt;
##Lobe Parcellation of 3T MR data - need help parametrization (Sylvain Bouix BWH, Priya Srinivasan BWH, Brad Davis Kitware)&lt;br /&gt;
##Finsler method (John Melonakos GATech, Marek Kubicki BWH)&lt;br /&gt;
##Group Analysis on DTI (Casey Goodlett Utah, Marek Kubicki BWH)&lt;br /&gt;
#[[DBP2:UNC|Longitudinal MRI Study of Early Brain Development in Autism]] (UNC: Heather Hazlett, Joseph Piven, PI)&lt;br /&gt;
##Work Flow Tool for regional cortical thickness pipeline (Clement Vachet UNC)&lt;br /&gt;
##NITRC registration of cortical thickness modules (Clement Vachet UNC)&lt;br /&gt;
##DTI tools for a) DWI preparation and b) DTI atlas building (Zhexing Liu UNC) &lt;br /&gt;
#[[DBP2:MIND|Analysis of Brain Lesions in Lupus]] (MIND/UNM: Jeremy Bockholt, Charles Gasparovic PI)&lt;br /&gt;
##[[DBP2:MIND:RoadmapProject|Finish Roadmap Project]]&lt;br /&gt;
##[[DBP2:MIND:LongitudinalRegistrationProject|Longitudinal Registration]]&lt;br /&gt;
##[[DBP2:MIND:BeyondLesionsProject|Beyond Lesions]]&lt;br /&gt;
#[[DBP2:JHU|Segmentation and Registration Tools for Robotic Prostate Intervention]] (Queens/JHU: Gabor Fichtinger, PI)&lt;br /&gt;
##[[DBP2:JHU:Roadmap|Trans-Rectal Prostate Biopsy module (David Gobbi, Gabor Fichtinger, Queens/JHU)]]&lt;br /&gt;
##[[Projects:ProstateSegmentation|Prostate Segmentation and Registration (Yi Gao GATech, Gabor Fichtinger JHU)]]&lt;br /&gt;
##Hardware/software overlay for percutaneous intervention (Siddharth Vikal, Gabor Fichtinger, Queens/JHU)&lt;br /&gt;
&lt;br /&gt;
===Other Projects===&lt;br /&gt;
#[[2008_Summer_Project_Week:EddyCurrentCorrection|Eddy current and head motion correction of DWIs]] (Ran Tao, Utah, Sylvain Bouix, BWH, Xiaodong Tao, GE, Tom Fletcher, Utah)&lt;br /&gt;
#Integraton of groupwise b-spline registration into atlas building (Casey Goodlett, Serdar Balci)&lt;br /&gt;
# CVS / SVN auto synchronization&lt;br /&gt;
# 3D Widgets in Slicer&lt;br /&gt;
## Issues with existing widgets&lt;br /&gt;
## Design of new widgets&lt;br /&gt;
# Batch processing in the NAMIC Kit (Julien, Marco, Steve, Jim)&lt;br /&gt;
# Module Chaining (Marco, Jim, Steve, Dan B., Luca)&lt;br /&gt;
# Nonlinear transforms (Jim, Steve, Luis)&lt;br /&gt;
## TransformToWorld/TransformFromWorld, integration with slice viewing&lt;br /&gt;
# Slicer3, XNAT integration, and desigining XCEDE Web Services (Dan M., Steve, Julien, Dan B.)&lt;br /&gt;
## Review and enrich use cases&lt;br /&gt;
# Python in Slicer (Dan B., Michael Halle, Steve, Luca)&lt;br /&gt;
# Performance Tuning of Fiducials using the EventBroker and other tools (Nicole, Alex, Steve, Will)&lt;br /&gt;
# GUI Tweaking (Wendy, Sebastien) [http://www.na-mic.org/Bug/view.php?id=242]&lt;br /&gt;
# [[2008_Summer_Project_Week:EddyCurrentCorrection|fMRI connectivity]]  (Bryce Kim, MIT)&lt;br /&gt;
&lt;br /&gt;
===External Collaborations===&lt;br /&gt;
#[[NA-MIC/Projects/Collaboration/UWA-Perth]] (Adam Wittek)&lt;br /&gt;
#[[NA-MIC/Projects/Collaboration/MRSI Module for Slicer]] (Bjoern Menze)&lt;br /&gt;
#[[NA-MIC/Projects/Collaboration/NIREP: Non-rigid Image Registration Evaluation]] (Gary Christensen Group)&lt;br /&gt;
#[[NA-MIC/Projects/Collaboration/Lung Atlas]] (Gary Christensen Group)&lt;br /&gt;
#Non-rigid image registration (Gary Christensen Group)&lt;br /&gt;
#[[NA-MIC/Projects/Collaboration/SARP phantom]] (Keith Gunderson)&lt;br /&gt;
#FMA (Protege) links to Slicer (Vish, Mike, Florin, Jim, Steve, Wendy)&lt;br /&gt;
#[[NA-MIC/Projects/External Collaboration/Measuring Alcohol and Stress Interaction]]&lt;br /&gt;
#[[NA-MIC/Projects/External Collaboration/Slicer3-vmtk Integration]] (Luca Antiga)&lt;br /&gt;
#[[NA-MIC/Projects/External Collaboration/Mesh Generation Summer 2008]] (Iowa Group)&lt;br /&gt;
&lt;br /&gt;
===Non-Medical Collaborations===&lt;br /&gt;
#[[NA-MIC/Projects/Non-Medical Collaborations/Astronomical Medicine|Astronomical Medicine]] (Harvard IIC: Douglas Alan, Michael Halle)&lt;br /&gt;
&lt;br /&gt;
==Attendee List==&lt;br /&gt;
# Ron Kikinis, BWH&lt;br /&gt;
# Carl-Fredrik Westin, BWH&lt;br /&gt;
# Gary Christensen, The University of Iowa&lt;br /&gt;
# Jeffrey Hawley, Gary Christensen's student&lt;br /&gt;
# Kate Raising, Gary Christensen's student&lt;br /&gt;
# Nathan Fritze, Gary Christensen's student&lt;br /&gt;
# Paul Song, Gary Christensen's student&lt;br /&gt;
# Cheng Zhang, Gary Christensen's student&lt;br /&gt;
# Ying Wei, Gary Christensen's student&lt;br /&gt;
# Nathan Burnette, The University of Iowa&lt;br /&gt;
# Hans Johnson, The University of Iowa&lt;br /&gt;
# Vincent Magnotta, The University of Iowa&lt;br /&gt;
# Keith Gunderson, The University of Iowa&lt;br /&gt;
# Steve Pieper, Isomics, Core 2/6&lt;br /&gt;
# Dana C. Peters, BIDMC Harvard Medical&lt;br /&gt;
# Jason Taclas, BIDMC Harvard Medical&lt;br /&gt;
# Nicole Aucoin, BWH, Core 2&lt;br /&gt;
# Will Schroeder, Kitware, Cores 2/4&lt;br /&gt;
# Sebastien Barre, Kitware, Core 2&lt;br /&gt;
# Julien Jomier, Kitware, Core 2&lt;br /&gt;
# Luis Ibanez, Kitware, Core 2&lt;br /&gt;
# Curtis Lisle, KnowledgeVis, Core 2&lt;br /&gt;
# Katie Hayes, BWH, Core 2&lt;br /&gt;
# Randy Gollub, MGH, Core 5&lt;br /&gt;
# Clement Vachet, UNC, Core 3&lt;br /&gt;
# Zhexing Liu, UNC, Core 1/3&lt;br /&gt;
# Casey Goodlett, Utah, Core 1&lt;br /&gt;
# Marcel Prastawa, Utah, Core 1&lt;br /&gt;
# Jeffrey Grethe, UCSD, Core 2&lt;br /&gt;
# Marco Ruiz, UCSD, Core 2&lt;br /&gt;
# Zhen Qian, Rutgers University&lt;br /&gt;
# Jinghao Zhou, Rutgers University&lt;br /&gt;
# Luca Antiga, Mario Negri Institute&lt;br /&gt;
# Adam Wittek, The University of Western Australia&lt;br /&gt;
# Grand Joldes, The University of Western Australia&lt;br /&gt;
# Jamie Berger, The University of Western Australia&lt;br /&gt;
# Serdar Balci, MIT, Core 1&lt;br /&gt;
# Bryce Kim, MIT, Core1&lt;br /&gt;
# Tina Kapur, BWH, Core 6&lt;br /&gt;
# Carling Cheung, Robarts Research Institute / The University of Western Ontario&lt;br /&gt;
# Danielle Pace, Robarts Research Institute / The University of Western Ontario&lt;br /&gt;
# Sean Megason, Dept of Systems Biology, Harvard Medical School&lt;br /&gt;
# Alex Gouaillard, Dept of Systems Biology, Harvard Medical School&lt;br /&gt;
# Kishore Mosaliganti, Dept of Systems Biology, Harvard Medical School&lt;br /&gt;
# Arnaud Gelas, Dept of Systems Biology, Harvard Medical School&lt;br /&gt;
# Sonia Pujol, Surgical Planning Laboratory, BWH&lt;br /&gt;
# Bjoern Menze, (then) Surgical Planning Laboratory, BWH&lt;br /&gt;
# Alex Yarmarkovich, Isomics, Core 2&lt;br /&gt;
# Sylvain Bouix, BWH, Core 3&lt;br /&gt;
# Priya Srinivasan, BWH, Core 3&lt;br /&gt;
# Chris Churas, UCSD, Core 2&lt;br /&gt;
# John Melonakos, Georgia Tech, Core 1&lt;br /&gt;
# Yi Gao, Georgia Tech, Core 1&lt;br /&gt;
# Tauseef Rehman, Georgia Tech, Core 1&lt;br /&gt;
# Clare Poynton, MIT, Core 1&lt;br /&gt;
# H. Jeremy Bockholt, MRN Lupus DBP Core 3&lt;br /&gt;
# Mark Scully, MRN Lupus DBP Core 3&lt;br /&gt;
# Gabor Fichtinger, Queen's, Core 3&lt;br /&gt;
# David Gobbi, Queen's, Core 3&lt;br /&gt;
# Purang Abolmaesumi, Queen's, Core 3&lt;br /&gt;
# Siddharth Vikal, Queen's, Core 3&lt;br /&gt;
# Daniel Blezek, Mayo&lt;br /&gt;
# Csaba Csoma, JHU, Core 3&lt;br /&gt;
# Ran Tao, University of Utah, Core 1&lt;br /&gt;
# Jim Miller, GE Research, Core 2&lt;br /&gt;
# Xiaodong Tao, GE Research, Core 2&lt;br /&gt;
# Dirk Padfield, GE Research, Core 2&lt;br /&gt;
# Viswanath Avasarala, GE Research, NAC&lt;br /&gt;
# Dan Marcus, Washington University   &lt;br /&gt;
# Tim Olsen, Washington University   &lt;br /&gt;
# Kevin Archie, Washington University   &lt;br /&gt;
# Misha Milchenko, Washington University&lt;br /&gt;
# Wendy Plesniak, BWH, Core 2&lt;br /&gt;
# Demian Wasserman, INRIA, LMI-collaborator&lt;br /&gt;
# Xenophon Papademetris, Yale, Collaborator&lt;br /&gt;
# Xenophon P's postdoc, Yale, Collaborator&lt;br /&gt;
# Xenophon P's student, Yale, Collaborator&lt;br /&gt;
# Vidya Rajagopalan, Virginia Tech, Student of Chris Wyatt, External Collaborator&lt;br /&gt;
# Greg Sharp, MGH, External Collaborator&lt;br /&gt;
# Marta Peroni, MGH, External Collaborator&lt;br /&gt;
# Toru Higaki, Hiroshima Univ., Japan, External collaborator (Hata)&lt;br /&gt;
# Jacek Kukluk, BWH,&lt;br /&gt;
# Nobuhiko Hata, BWH&lt;br /&gt;
# Junichi Tokuda, BWH&lt;br /&gt;
# Haying Liu, BWH&lt;br /&gt;
# Ragini Verma, UPenn (June 24)&lt;br /&gt;
# Luke Bloy, UPenn (Ragini Verma's student) (June 24)&lt;br /&gt;
# Yang Li, UPenn (Ragini's postdoc) (June 24)&lt;br /&gt;
# Jack Blevins, Acoustic Med, Collaborator&lt;br /&gt;
# Nikos Chrisochoides, College of William and Mary, External collaborator (June 23)&lt;br /&gt;
# Andriy Fedorov, College of William and Mary, External collaborator&lt;br /&gt;
# Carlos Sánchez Mendoza, BWH &lt;br /&gt;
# Kilian Pohl, BWH&lt;br /&gt;
# Pratik Patel, Brainlab, Collaborator&lt;br /&gt;
# Marianna Jakab, BWH&lt;br /&gt;
# Nathan Hageman, UCLA&lt;br /&gt;
# Douglas Alan, Harvard IIC, External Collaborator&lt;br /&gt;
# Tammy Riklin Raviv, MIT&lt;br /&gt;
# Peter Kazanzides, JHU, Collaborator&lt;br /&gt;
# Scott Hoge, BWH, (Wed, Jun 25)&lt;br /&gt;
#*WE HAVE REACHED CAPACITY. REGISTRATION IS CLOSED. [[User:Tkapur|Tkapur]] 19:42, 6 June 2008 (UTC)&lt;br /&gt;
&lt;br /&gt;
==Pictures==&lt;/div&gt;</summary>
		<author><name>Ybkim</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=2008_Summer_Project_Week&amp;diff=26627</id>
		<title>2008 Summer Project Week</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=2008_Summer_Project_Week&amp;diff=26627"/>
		<updated>2008-06-10T19:15:32Z</updated>

		<summary type="html">&lt;p&gt;Ybkim: /* Other Projects */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Back to [[Engineering:Programming_Events|Programming/Project Events]]&lt;br /&gt;
&lt;br /&gt;
[[Image:ProjectWeek-2008.png|thumb|220px|right|Summer 2008]]&lt;br /&gt;
&lt;br /&gt;
== Logistics ==&lt;br /&gt;
&lt;br /&gt;
'''Dates:''' June 23-27, 2008&lt;br /&gt;
&lt;br /&gt;
'''Location:''' MIT. [[Meeting_Locations:MIT_Grier_A_%26B|Grier Rooms A &amp;amp; B: 34-401A &amp;amp; 34-401B]].&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
'''Registration Fee:''' $260 (this will cover the cost of breakfast, lunch and coffee breaks for the week). Due by Friday, June 13th, 2008. Please make checks out to &amp;quot;Massachusetts Institute of Technology&amp;quot; and mail to: Donna Kaufman, MIT, 77 Massachusetts Ave., 38-409a, Cambridge, MA 02139&lt;br /&gt;
&lt;br /&gt;
'''Registration Method''' Please add your name to the attendee list below (create namic wiki account if you don't have one, by clicking on the &amp;quot;login/create account&amp;quot; link on the top right corner of this page), and then mail a check to Donna Kaufman at the address above.&lt;br /&gt;
&lt;br /&gt;
If you are attending for one day only, the registration fee is not required.&lt;br /&gt;
&lt;br /&gt;
'''Hotel:''' We have a group rate of $239/night (plus tax) for a room with either 1 king or 2 queen beds at the [http://www.hotelatmit.com Hotel at MIT (now called Le Meridien)]. [http://www.starwoodmeeting.com/StarGroupsWeb/booking/reservation?id=0805167317&amp;amp;key=4FD1B  Please click here to reserve.]This rate is good only through June 1.&lt;br /&gt;
&lt;br /&gt;
Here is some information about several other Boston area hotels that are convenient to NA-MIC events: [[Boston_Hotels|Boston_Hotels]]. Summer is tourist season in Boston, so please book your rooms early.&lt;br /&gt;
&lt;br /&gt;
([[Project Week Logistics Checklist|This is a checklist for the onsite planning items]])&lt;br /&gt;
&lt;br /&gt;
==Introduction to NA-MIC Project Week==&lt;br /&gt;
&lt;br /&gt;
NA-MIC Project Week is a hands on activity -- programming using the [[NA-MIC-Kit|NA-MIC Kit]], algorithm design, and clinical application -- that has become one of the major events in the [[NA-MIC-Kit|NA-MIC Kit]] calendar. This event is the seventh of the [[Engineering:Programming_Events|'''series''']]. It is held in the summer at MIT (typically the last week of June), and a shorter version is held in Salt Lake City in the winter (typically the second week of January).  &lt;br /&gt;
The main goal of these events if to move forward the deliverables of NA-MIC. NA-MIC participants and their collaborators are welcome to attend.  &lt;br /&gt;
&lt;br /&gt;
* NA-MIC Members: Participation in this event is voluntary -- if you don't think this will help you move forward in your work, there is no obligation to attend.&lt;br /&gt;
* Ideal candidates are those who want to contribute to the [[NA-MIC-Kit|NA-MIC Kit]], and those who can help make it happen.&lt;br /&gt;
* This is not an introduction to the components of the [[NA-MIC-Kit|NA-MIC Kit]].&lt;br /&gt;
* NA-MIC Core 1 (Algorithms) - bring your algorithms and code to work on in the company of Core 2 engineers and Core 3 scientists.&lt;br /&gt;
* NA-MIC Core 2 (Engineering) - bring your code for infrastructure and applications to extend the [[NA-MIC-Kit|NA-MIC Kit]] capabilities, integrate Core 1 algorithms, and refine workflows for Core 3.&lt;br /&gt;
* NA-MIC Core 3 (DBP) - bring your data to work on with the [[NA-MIC-Kit|NA-MIC Kit]] and get assistance and provide feedback to Core 1 scientists and Core 2 engineers.&lt;br /&gt;
* External Collaborators - if you are working on a project that uses the [[NA-MIC-Kit|NA-MIC kit]], and want to participate to get help from NA-MIC Engineering, please send an email to Tina Kapur (tkapur at bwh.harvard.edu).  Please note that the event is open to people outside NA-MIC, subject to availability.&lt;br /&gt;
* Everyone should '''bring a laptop'''. We will have four projectors.&lt;br /&gt;
* About half the time will be spent working on projects and the other half in project related discussions.&lt;br /&gt;
* You '''do''' need to be actively working on a NA-MIC related project in order to make this investment worthwhile for everyone.&lt;br /&gt;
&lt;br /&gt;
== Agenda==&lt;br /&gt;
* Monday &lt;br /&gt;
** noon-1pm lunch &lt;br /&gt;
**1pm: Welcome (Ron Kikinis)&lt;br /&gt;
** 1:05-3:30pm Introduce [[#Projects|Projects]] using templated wiki pages (all Project Leads) ([[NA-MIC/Projects/Theme/Template|Wiki Template]]) &lt;br /&gt;
** 3:30-5:30pm Start project work&lt;br /&gt;
* Tuesday &lt;br /&gt;
** 8:30am breakfast&lt;br /&gt;
** 9:00-9:45am: NA-MIC Software Process &lt;br /&gt;
** 10-10:30am [[Project Week 2008 Slicer 3.0 Update|Slicer 3.0 Update]] (Jim Miller, Steve Pieper)&lt;br /&gt;
** noon lunch&lt;br /&gt;
** 2:30-3:30pm: [[Project Week 2008 Special topic breakout: Non-Linear Registration]] &lt;br /&gt;
** 5:30pm adjourn for day&lt;br /&gt;
* Wednesday &lt;br /&gt;
** 8:30am breakfast&lt;br /&gt;
** 9:00-12pm [[Project Week 2008 Special topic breakout: ITK]] (Luis Ibanez)&lt;br /&gt;
** noon lunch&lt;br /&gt;
** 2:30-3:30pm: [[Project Week 2008 Special topic breakout: XNAT Database]] (Daniel Marcus)&lt;br /&gt;
** 5:30pm adjourn for day&lt;br /&gt;
* Thursday&lt;br /&gt;
** 8:30am breakfast&lt;br /&gt;
** noon lunch&lt;br /&gt;
**2:30-3:30pm [[Project Week 2008 Special topic breakout: GWE]] (Marco Ruiz)&lt;br /&gt;
** 5:30pm adjourn for day&lt;br /&gt;
* Friday &lt;br /&gt;
** 8:30am breakfast&lt;br /&gt;
** 10am-noon: Project Progress using update [[#Projects|Project Wiki pages]]&lt;br /&gt;
** noon lunch boxes and adjourn.  (Next one [[AHM_2009| in Utah the week of Jan 5, 2009]])&lt;br /&gt;
&lt;br /&gt;
== Preparation ==&lt;br /&gt;
&lt;br /&gt;
# Please make sure that you are on the http://public.kitware.com/cgi-bin/mailman/listinfo/na-mic-project-week mailing list&lt;br /&gt;
&lt;br /&gt;
# [[Engineering:TCON_2008|May 08 and May 15 TCON DBPs ONLY]] at 3pm ET to discuss NA-MIC DBP Projects ONLY. &lt;br /&gt;
# [[Engineering:TCON_2008|May 22 TCON#1]] at 3pm ET to discuss NA-MIC Engr Core Projects and Assign/Verify Teams&lt;br /&gt;
# [[Engineering:TCON_2008|May 29 TCON#2]] at 3pm ET to discuss NA-MIC ALGORITHMS Core Lead Projects.  Project leads should sign up for a slot [[Engineering:TCON_2008|here]]. Projects will be discussed in order of the signups. &lt;br /&gt;
# [[Engineering:TCON_2008|June 5 TCON#3]] at 3pm ET to discuss NA-MIC EXTERNAL Collaborations.  All NIH funded &amp;quot;collaborations with NCBC&amp;quot; leads should call. Project leads should sign up for a slot [[Engineering:TCON_2008|here]].  Projects will be discussed in order of the signups. &lt;br /&gt;
# [[Engineering:TCON_2008|June 12 TCON#4]] at 3pm ET to discuss NA-MIC EXTERNAL Collaborations.  All other collaboration leads should call. Project leads should sign up for a slot [[Engineering:TCON_2008|here]].  Projects will be discussed in order of the signups. &lt;br /&gt;
# [[Engineering:TCON_2008|June 19 TCON#5]] at 3pm ET to tie loose ends.  Anyone with un-addressed questions should call.&lt;br /&gt;
# By 3pm ET on June 12, 2008: [[NA-MIC/Projects/Theme/Template|Complete a templated wiki page for your project]]. Please do not edit the template page itself, but create a new page for your project and cut-and-paste the text from this template page.  If you have questions, please send an email to tkapur at bwh.harvard.edu.&lt;br /&gt;
# By 3pm on June 19, 2008: Create a directory for each project on the [[Engineering:SandBox|NAMIC Sandbox]] (Zack)&lt;br /&gt;
## Commit on each sandbox directory the code examples/snippets that represent our first guesses of appropriate methods. (Luis and Steve will help with this, as needed)&lt;br /&gt;
## Gather test images in any of the Data sharing resources we have (e.g. the BIRN). These ones don't have to be many. At least three different cases, so we can get an idea of the modality-specific characteristics of these images. Put the IDs of these data sets on the wiki page. (the participants must do this.)&lt;br /&gt;
## Setup nightly tests on a separate Dashboard, where we will run the methods that we are experimenting with. The test should post result images and computation time. (Zack)&lt;br /&gt;
# Please note that by the time we get to the project event, we should be trying to close off a project milestone rather than starting to work on one...&lt;br /&gt;
&lt;br /&gt;
== A History in Wiki Links ==&lt;br /&gt;
&lt;br /&gt;
A history of all the programming/project events in NA-MIC is available by following [[Engineering:Programming_Events|this link]].&lt;br /&gt;
&lt;br /&gt;
== Projects ==&lt;br /&gt;
&lt;br /&gt;
===DBP II===&lt;br /&gt;
These are projects by the new set of DBPS:&lt;br /&gt;
#[[DBP2:Harvard|Velocardio Facial Syndrome (VCFS) as a Genetic Model for Schizophrenia]] (Harvard: Marek Kubicki, PI)&lt;br /&gt;
##EPI-DWI Distortion correction (Sylvain Bouix BWH, Tauseef Rehman GATech)&lt;br /&gt;
##[[2008_Summer_Project_Week:EddyCurrentCorrection|EPI-DWI Eddy Current distortion correction]] (Sylvain Bouix BWH, Ran Tao Utah)&lt;br /&gt;
##Lobe Parcellation of 3T MR data - need help parametrization (Sylvain Bouix BWH, Priya Srinivasan BWH, Brad Davis Kitware)&lt;br /&gt;
##Finsler method (John Melonakos GATech, Marek Kubicki BWH)&lt;br /&gt;
##Group Analysis on DTI (Casey Goodlett Utah, Marek Kubicki BWH)&lt;br /&gt;
#[[DBP2:UNC|Longitudinal MRI Study of Early Brain Development in Autism]] (UNC: Heather Hazlett, Joseph Piven, PI)&lt;br /&gt;
##Work Flow Tool for regional cortical thickness pipeline (Clement Vachet UNC)&lt;br /&gt;
##NITRC registration of cortical thickness modules (Clement Vachet UNC)&lt;br /&gt;
##DTI tools for a) DWI preparation and b) DTI atlas building (Zhexing Liu UNC) &lt;br /&gt;
#[[DBP2:MIND|Analysis of Brain Lesions in Lupus]] (MIND/UNM: Jeremy Bockholt, Charles Gasparovic PI)&lt;br /&gt;
##[[DBP2:MIND:RoadmapProject|Finish Roadmap Project]]&lt;br /&gt;
##[[DBP2:MIND:LongitudinalRegistrationProject|Longitudinal Registration]]&lt;br /&gt;
##[[DBP2:MIND:BeyondLesionsProject|Beyond Lesions]]&lt;br /&gt;
#[[DBP2:JHU|Segmentation and Registration Tools for Robotic Prostate Intervention]] (Queens/JHU: Gabor Fichtinger, PI)&lt;br /&gt;
##[[DBP2:JHU:Roadmap|Trans-Rectal Prostate Biopsy module (David Gobbi, Gabor Fichtinger, Queens/JHU)]]&lt;br /&gt;
##[[Projects:ProstateSegmentation|Prostate Segmentation and Registration (Yi Gao GATech, Gabor Fichtinger JHU)]]&lt;br /&gt;
##Hardware/software overlay for percutaneous intervention (Siddharth Vikal, Gabor Fichtinger, Queens/JHU)&lt;br /&gt;
&lt;br /&gt;
===Other Projects===&lt;br /&gt;
#[[2008_Summer_Project_Week:EddyCurrentCorrection|Eddy current and head motion correction of DWIs]] (Ran Tao, Utah, Sylvain Bouix, BWH, Xiaodong Tao, GE, Tom Fletcher, Utah)&lt;br /&gt;
#Integraton of groupwise b-spline registration into atlas building (Casey Goodlett, Serdar Balci)&lt;br /&gt;
# CVS / SVN auto synchronization&lt;br /&gt;
# 3D Widgets in Slicer&lt;br /&gt;
## Issues with existing widgets&lt;br /&gt;
## Design of new widgets&lt;br /&gt;
# Batch processing in the NAMIC Kit (Julien, Marco, Steve, Jim)&lt;br /&gt;
# Module Chaining (Marco, Jim, Steve, Dan B., Luca)&lt;br /&gt;
# Nonlinear transforms (Jim, Steve, Luis)&lt;br /&gt;
## TransformToWorld/TransformFromWorld, integration with slice viewing&lt;br /&gt;
# Slicer3, XNAT integration, and desigining XCEDE Web Services (Dan M., Steve, Julien, Dan B.)&lt;br /&gt;
## Review and enrich use cases&lt;br /&gt;
# Python in Slicer (Dan B., Michael Halle, Steve, Luca)&lt;br /&gt;
# Performance Tuning of Fiducials using the EventBroker and other tools (Nicole, Alex, Steve, Will)&lt;br /&gt;
# GUI Tweaking (Wendy, Sebastien) [http://www.na-mic.org/Bug/view.php?id=242]&lt;br /&gt;
# fMRI connectivity (Bryce Kim, MIT)&lt;br /&gt;
&lt;br /&gt;
===External Collaborations===&lt;br /&gt;
#[[NA-MIC/Projects/Collaboration/UWA-Perth]] (Adam Wittek)&lt;br /&gt;
#[[NA-MIC/Projects/Collaboration/MRSI Module for Slicer]] (Bjoern Menze)&lt;br /&gt;
#[[NA-MIC/Projects/Collaboration/NIREP: Non-rigid Image Registration Evaluation]] (Gary Christensen Group)&lt;br /&gt;
#[[NA-MIC/Projects/Collaboration/Lung Atlas]] (Gary Christensen Group)&lt;br /&gt;
#Non-rigid image registration (Gary Christensen Group)&lt;br /&gt;
#[[NA-MIC/Projects/Collaboration/SARP phantom]] (Keith Gunderson)&lt;br /&gt;
#FMA (Protege) links to Slicer (Vish, Mike, Florin, Jim, Steve, Wendy)&lt;br /&gt;
#[[NA-MIC/Projects/External Collaboration/Measuring Alcohol and Stress Interaction]]&lt;br /&gt;
#[[NA-MIC/Projects/External Collaboration/Slicer3-vmtk Integration]] (Luca Antiga)&lt;br /&gt;
#[[NA-MIC/Projects/External Collaboration/Mesh Generation Summer 2008]] (Iowa Group)&lt;br /&gt;
&lt;br /&gt;
===Non-Medical Collaborations===&lt;br /&gt;
#[[NA-MIC/Projects/Non-Medical Collaborations/Astronomical Medicine|Astronomical Medicine]] (Harvard IIC: Douglas Alan, Michael Halle)&lt;br /&gt;
&lt;br /&gt;
==Attendee List==&lt;br /&gt;
# Ron Kikinis, BWH&lt;br /&gt;
# Carl-Fredrik Westin, BWH&lt;br /&gt;
# Gary Christensen, The University of Iowa&lt;br /&gt;
# Jeffrey Hawley, Gary Christensen's student&lt;br /&gt;
# Kate Raising, Gary Christensen's student&lt;br /&gt;
# Nathan Fritze, Gary Christensen's student&lt;br /&gt;
# Paul Song, Gary Christensen's student&lt;br /&gt;
# Cheng Zhang, Gary Christensen's student&lt;br /&gt;
# Ying Wei, Gary Christensen's student&lt;br /&gt;
# Nathan Burnette, The University of Iowa&lt;br /&gt;
# Hans Johnson, The University of Iowa&lt;br /&gt;
# Vincent Magnotta, The University of Iowa&lt;br /&gt;
# Keith Gunderson, The University of Iowa&lt;br /&gt;
# Steve Pieper, Isomics, Core 2/6&lt;br /&gt;
# Dana C. Peters, BIDMC Harvard Medical&lt;br /&gt;
# Jason Taclas, BIDMC Harvard Medical&lt;br /&gt;
# Nicole Aucoin, BWH, Core 2&lt;br /&gt;
# Will Schroeder, Kitware, Cores 2/4&lt;br /&gt;
# Sebastien Barre, Kitware, Core 2&lt;br /&gt;
# Julien Jomier, Kitware, Core 2&lt;br /&gt;
# Luis Ibanez, Kitware, Core 2&lt;br /&gt;
# Curtis Lisle, KnowledgeVis, Core 2&lt;br /&gt;
# Katie Hayes, BWH, Core 2&lt;br /&gt;
# Randy Gollub, MGH, Core 5&lt;br /&gt;
# Clement Vachet, UNC, Core 3&lt;br /&gt;
# Zhexing Liu, UNC, Core 1/3&lt;br /&gt;
# Casey Goodlett, Utah, Core 1&lt;br /&gt;
# Marcel Prastawa, Utah, Core 1&lt;br /&gt;
# Jeffrey Grethe, UCSD, Core 2&lt;br /&gt;
# Marco Ruiz, UCSD, Core 2&lt;br /&gt;
# Zhen Qian, Rutgers University&lt;br /&gt;
# Jinghao Zhou, Rutgers University&lt;br /&gt;
# Luca Antiga, Mario Negri Institute&lt;br /&gt;
# Adam Wittek, The University of Western Australia&lt;br /&gt;
# Grand Joldes, The University of Western Australia&lt;br /&gt;
# Jamie Berger, The University of Western Australia&lt;br /&gt;
# Serdar Balci, MIT, Core 1&lt;br /&gt;
# Bryce Kim, MIT, Core1&lt;br /&gt;
# Tina Kapur, BWH, Core 6&lt;br /&gt;
# Carling Cheung, Robarts Research Institute / The University of Western Ontario&lt;br /&gt;
# Danielle Pace, Robarts Research Institute / The University of Western Ontario&lt;br /&gt;
# Sean Megason, Dept of Systems Biology, Harvard Medical School&lt;br /&gt;
# Alex Gouaillard, Dept of Systems Biology, Harvard Medical School&lt;br /&gt;
# Kishore Mosaliganti, Dept of Systems Biology, Harvard Medical School&lt;br /&gt;
# Arnaud Gelas, Dept of Systems Biology, Harvard Medical School&lt;br /&gt;
# Sonia Pujol, Surgical Planning Laboratory, BWH&lt;br /&gt;
# Bjoern Menze, (then) Surgical Planning Laboratory, BWH&lt;br /&gt;
# Alex Yarmarkovich, Isomics, Core 2&lt;br /&gt;
# Sylvain Bouix, BWH, Core 3&lt;br /&gt;
# Priya Srinivasan, BWH, Core 3&lt;br /&gt;
# Chris Churas, UCSD, Core 2&lt;br /&gt;
# John Melonakos, Georgia Tech, Core 1&lt;br /&gt;
# Yi Gao, Georgia Tech, Core 1&lt;br /&gt;
# Tauseef Rehman, Georgia Tech, Core 1&lt;br /&gt;
# Clare Poynton, MIT, Core 1&lt;br /&gt;
# H. Jeremy Bockholt, MRN Lupus DBP Core 3&lt;br /&gt;
# Mark Scully, MRN Lupus DBP Core 3&lt;br /&gt;
# Gabor Fichtinger, Queen's, Core 3&lt;br /&gt;
# David Gobbi, Queen's, Core 3&lt;br /&gt;
# Purang Abolmaesumi, Queen's, Core 3&lt;br /&gt;
# Siddharth Vikal, Queen's, Core 3&lt;br /&gt;
# Daniel Blezek, Mayo&lt;br /&gt;
# Csaba Csoma, JHU, Core 3&lt;br /&gt;
# Ran Tao, University of Utah, Core 1&lt;br /&gt;
# Jim Miller, GE Research, Core 2&lt;br /&gt;
# Xiaodong Tao, GE Research, Core 2&lt;br /&gt;
# Dirk Padfield, GE Research, Core 2&lt;br /&gt;
# Viswanath Avasarala, GE Research, NAC&lt;br /&gt;
# Dan Marcus, Washington University   &lt;br /&gt;
# Tim Olsen, Washington University   &lt;br /&gt;
# Kevin Archie, Washington University   &lt;br /&gt;
# Misha Milchenko, Washington University&lt;br /&gt;
# Wendy Plesniak, BWH, Core 2&lt;br /&gt;
# Demian Wasserman, INRIA, LMI-collaborator&lt;br /&gt;
# Xenophon Papademetris, Yale, Collaborator&lt;br /&gt;
# Xenophon P's postdoc, Yale, Collaborator&lt;br /&gt;
# Xenophon P's student, Yale, Collaborator&lt;br /&gt;
# Vidya Rajagopalan, Virginia Tech, Student of Chris Wyatt, External Collaborator&lt;br /&gt;
# Greg Sharp, MGH, External Collaborator&lt;br /&gt;
# Marta Peroni, MGH, External Collaborator&lt;br /&gt;
# Toru Higaki, Hiroshima Univ., Japan, External collaborator (Hata)&lt;br /&gt;
# Jacek Kukluk, BWH,&lt;br /&gt;
# Nobuhiko Hata, BWH&lt;br /&gt;
# Junichi Tokuda, BWH&lt;br /&gt;
# Haying Liu, BWH&lt;br /&gt;
# Ragini Verma, UPenn (June 24)&lt;br /&gt;
# Luke Bloy, UPenn (Ragini Verma's student) (June 24)&lt;br /&gt;
# Yang Li, UPenn (Ragini's postdoc) (June 24)&lt;br /&gt;
# Jack Blevins, Acoustic Med, Collaborator&lt;br /&gt;
# Nikos Chrisochoides, College of William and Mary, External collaborator (June 23)&lt;br /&gt;
# Andriy Fedorov, College of William and Mary, External collaborator&lt;br /&gt;
# Carlos Sánchez Mendoza, BWH &lt;br /&gt;
# Kilian Pohl, BWH&lt;br /&gt;
# Pratik Patel, Brainlab, Collaborator&lt;br /&gt;
# Marianna Jakab, BWH&lt;br /&gt;
# Nathan Hageman, UCLA&lt;br /&gt;
# Douglas Alan, Harvard IIC, External Collaborator&lt;br /&gt;
# Tammy Riklin Raviv, MIT&lt;br /&gt;
# Peter Kazanzides, JHU, Collaborator&lt;br /&gt;
# Scott Hoge, BWH, (Wed, Jun 25)&lt;br /&gt;
#*WE HAVE REACHED CAPACITY. REGISTRATION IS CLOSED. [[User:Tkapur|Tkapur]] 19:42, 6 June 2008 (UTC)&lt;br /&gt;
&lt;br /&gt;
==Pictures==&lt;/div&gt;</summary>
		<author><name>Ybkim</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:fMRIClustering&amp;diff=24721</id>
		<title>Projects:fMRIClustering</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:fMRIClustering&amp;diff=24721"/>
		<updated>2008-05-16T20:49:35Z</updated>

		<summary type="html">&lt;p&gt;Ybkim: /* Key Investigators */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Back to [[NA-MIC_Internal_Collaborations:fMRIAnalysis|NA-MIC Collaborations]], [[Algorithm:MIT|MIT Algorithms]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
&lt;br /&gt;
= fMRI Clustering =&lt;br /&gt;
&lt;br /&gt;
One of the major goals in analysis of fMRI data is the detection of networks in the brain with similar functional behavior. A wide variety of methods  including hypothesis-driven statistical tests, unsupervised learning methods such as PCA and ICA, and different clustering algorithms have been employed to find these networks. This project aims to particularly study application of model-based clustering algorithms in identification of functional connectivity in the brain. &lt;br /&gt;
&lt;br /&gt;
= Description =&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
'''''Generative Model for Functional Connectivity'''''&lt;br /&gt;
&lt;br /&gt;
In the classical functional connectivity analysis, networks of interest are&lt;br /&gt;
defined based on correlation with the mean time course of a user-selected&lt;br /&gt;
`seed' region. Further, the user has to also specify a subject-specific threshold at which correlation&lt;br /&gt;
values are deemed significant. In this project, we simultaneously estimate the optimal&lt;br /&gt;
representative time courses that summarize the fMRI data well and&lt;br /&gt;
the partition of the volume into a set of disjoint regions that are best&lt;br /&gt;
explained by these representative time courses. This approach to functional connectivity analysis offers two&lt;br /&gt;
advantages. First, is removes the sensitivity of the analysis to the details&lt;br /&gt;
of the seed selection. Second, it substantially simplifies group analysis&lt;br /&gt;
by eliminating the need for the subject-specific threshold. Our experimental results indicate that&lt;br /&gt;
the functional segmentation provides a robust, anatomically meaningful&lt;br /&gt;
and consistent model for functional connectivity in fMRI.&lt;br /&gt;
&lt;br /&gt;
We formulate the problem of characterizing connectivity as a partition of voxels into subsets that are well characterized by a certain number of representative hypotheses, or time courses, based on the similarity of their time courses to each hypothesis. We model the fMRI signal at each voxel as generated by a mixture of Gaussian distributions whose centers are the desired representative time courses. Using the EM algorithm to solve the corresponding model-fitting problem, we alternatively estimate the representative time courses and cluster assignments to improve our random initialization. &lt;br /&gt;
&lt;br /&gt;
''' ''Experimental Results'' '''&lt;br /&gt;
&lt;br /&gt;
We used data from 7 subjects with a diverse set of visual experiments including localizer, morphing, rest, internal tasks, and movie. The functional scans were pre-processed for motion artifacts, manually aligned into the Talairach coordinate system, detrended (removing linear trends in the&lt;br /&gt;
baseline activation) and smoothed (8mm kernel).&lt;br /&gt;
&lt;br /&gt;
Fig. 1 shows the 2-system partition extracted in each subject independently&lt;br /&gt;
of all others. It also displays the boundaries of the intrinsic system determined&lt;br /&gt;
through the traditional seed selection, showing good agreement between the two&lt;br /&gt;
partitions. Fig. 2 presents the results of further clustering the stimulus-driven cluster into two clusters independently for each subject. &lt;br /&gt;
&lt;br /&gt;
&amp;lt;table&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt; &amp;lt;th&amp;gt; '''Fig 1. 2-System Parcelation. Results for all 7 subjects.''' &amp;lt;th&amp;gt; '''Fig 2. 3-System Parcelation. Results for all 7 subjects.''' &lt;br /&gt;
&amp;lt;tr&amp;gt; &amp;lt;td align=&amp;quot;center&amp;quot;&amp;gt; &lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation2_shb1_4.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation2_shb5_6.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation2_shb7.png |400px]]&lt;br /&gt;
&amp;lt;td align=&amp;quot;center&amp;quot;&amp;gt;&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb1_3.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb4_5.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb6.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb7.png |400px]]&lt;br /&gt;
&amp;lt;/table&amp;gt;&lt;br /&gt;
&lt;br /&gt;
Fig.3 presents the group average of the subject-specific 2-system maps. Color shading shows the proportion of subjects whose clustering agreed with the majority label. Fig. 4 shows the group average of a further parcelation of the intrinsic system, i.e., one of two clusters associated with the non-stimulus-driven regions. In order to present a validation of the method, we compare these results with the conventional scheme for detection of visually responsive areas. In Fig. 5, color shows the statistical parametric map while solid lines indicate the boundaries of the visual system obtained through clustering. The result illustrate the agreement between the two methods.&lt;br /&gt;
&lt;br /&gt;
&amp;lt;table&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&amp;lt;th&amp;gt; '''Fig 3. 2-System Parcellation. Group-wise result.'''&lt;br /&gt;
&amp;lt;tr&amp;gt; &amp;lt;td align=&amp;quot;center&amp;quot;&amp;gt;&lt;br /&gt;
{|&lt;br /&gt;
|+ &lt;br /&gt;
|valign=&amp;quot;top&amp;quot;|[[Image:mit_fmri_clustering_parcellation2_xsub.png |thumb|700px]]&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/table&amp;gt;&lt;br /&gt;
&lt;br /&gt;
{|&lt;br /&gt;
|+ '''Fig 4. Validation: Parcelation of the intrinsic system.'''&lt;br /&gt;
|valign=&amp;quot;top&amp;quot;|[[Image:mit_fmri_clustering_intrinsicsystem.png |thumb|650px]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
{|&lt;br /&gt;
|+ '''Fig 5. Validation: Visual system.'''&lt;br /&gt;
|valign=&amp;quot;top&amp;quot;|[[Image:mit_fmri_clustering_validation.png |thumb|1150px]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''' ''Clustering Study of Domain Specificity in High Level Visual Cortex'' '''&lt;br /&gt;
&lt;br /&gt;
As a more specific application of clustering model-based algorithms, we are currently investigating devising clustering algorithms for detection of functional connectivity in high-level visual cortex. It is suggested that there are regions in the visual cortex with high selectivity to certain categories of visual stimuli. Currently, the conventional method for detection of these methods is based on statistical tests comparing response of each voxel in the brain to different visual categories to see if it shows considerably higher activation to one category. For example, the well-known FFA (Fusiform Face Area) is the set of voxels which show high activation to faces when compared to objects. We are working on using the clustering the visual cortex as a means to make this analysis automatic and further discover new structures in the high-level visual cortex.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''' ''Comparison of Data-Driven Analysis Methods for Identiﬁcation of Functional Connectivity in fMRI'' '''&lt;br /&gt;
&lt;br /&gt;
Although ICA and clustering rely on very diﬀerent assumptions on the underlying distributions, they produce surprisingly similar results for signals with large variation. Our main goal is to evaluate and compare the performance of ICA and clustering based on Gaussian mixture model (GMM) for identiﬁcation of functional connectivity. Using the synthetic data with artiﬁcial activations and artifacts under various levels of length of the time course and signal-to-noise ratio of the data, we compare both spatial maps and their associated time courses estimated by ICA and GMM to each other and to the ground truth. We choose the number of sources via the model selection scheme, and compare all of the resulting components of GMM and ICA, not just the task-related components, after we match them component-wise using the Hungarian algorithm. This comparison scheme is veriﬁed in a high level visual cortex fMRI study. We ﬁnd that ICA requires a smaller number of total components to extract the task-related components, but also needs a large number of total components to describe the entire data. We are currently applying ICA and clustering methods to connectivity analysis of schizophrenia patients.&lt;br /&gt;
&lt;br /&gt;
= Key Investigators =&lt;br /&gt;
&lt;br /&gt;
* MIT Algorithms: Danial Lashkari, Y. Bryce Kim, Polina Golland, Nancy Kanwisher.&lt;br /&gt;
* Harvard DBP 2: J. Oh, Marek Kubicki.&lt;br /&gt;
&lt;br /&gt;
= Publications =&lt;br /&gt;
&lt;br /&gt;
''In print''&lt;br /&gt;
&lt;br /&gt;
* [http://www.na-mic.org/pages/Special:Publications?text=fMRI+Clustering&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;
''In press''&lt;br /&gt;
&lt;br /&gt;
* D. Lashkari, P. Golland. Convex Clustering with Exemplar-Based Models. In NIPS: Advances in Neural Information Processing Systems, 2007.&lt;br /&gt;
&lt;br /&gt;
[[Category:fMRI]]&lt;/div&gt;</summary>
		<author><name>Ybkim</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:fMRIClustering&amp;diff=24717</id>
		<title>Projects:fMRIClustering</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:fMRIClustering&amp;diff=24717"/>
		<updated>2008-05-16T20:45:14Z</updated>

		<summary type="html">&lt;p&gt;Ybkim: /* Description */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Back to [[NA-MIC_Internal_Collaborations:fMRIAnalysis|NA-MIC Collaborations]], [[Algorithm:MIT|MIT Algorithms]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
&lt;br /&gt;
= fMRI Clustering =&lt;br /&gt;
&lt;br /&gt;
One of the major goals in analysis of fMRI data is the detection of networks in the brain with similar functional behavior. A wide variety of methods  including hypothesis-driven statistical tests, unsupervised learning methods such as PCA and ICA, and different clustering algorithms have been employed to find these networks. This project aims to particularly study application of model-based clustering algorithms in identification of functional connectivity in the brain. &lt;br /&gt;
&lt;br /&gt;
= Description =&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
'''''Generative Model for Functional Connectivity'''''&lt;br /&gt;
&lt;br /&gt;
In the classical functional connectivity analysis, networks of interest are&lt;br /&gt;
defined based on correlation with the mean time course of a user-selected&lt;br /&gt;
`seed' region. Further, the user has to also specify a subject-specific threshold at which correlation&lt;br /&gt;
values are deemed significant. In this project, we simultaneously estimate the optimal&lt;br /&gt;
representative time courses that summarize the fMRI data well and&lt;br /&gt;
the partition of the volume into a set of disjoint regions that are best&lt;br /&gt;
explained by these representative time courses. This approach to functional connectivity analysis offers two&lt;br /&gt;
advantages. First, is removes the sensitivity of the analysis to the details&lt;br /&gt;
of the seed selection. Second, it substantially simplifies group analysis&lt;br /&gt;
by eliminating the need for the subject-specific threshold. Our experimental results indicate that&lt;br /&gt;
the functional segmentation provides a robust, anatomically meaningful&lt;br /&gt;
and consistent model for functional connectivity in fMRI.&lt;br /&gt;
&lt;br /&gt;
We formulate the problem of characterizing connectivity as a partition of voxels into subsets that are well characterized by a certain number of representative hypotheses, or time courses, based on the similarity of their time courses to each hypothesis. We model the fMRI signal at each voxel as generated by a mixture of Gaussian distributions whose centers are the desired representative time courses. Using the EM algorithm to solve the corresponding model-fitting problem, we alternatively estimate the representative time courses and cluster assignments to improve our random initialization. &lt;br /&gt;
&lt;br /&gt;
''' ''Experimental Results'' '''&lt;br /&gt;
&lt;br /&gt;
We used data from 7 subjects with a diverse set of visual experiments including localizer, morphing, rest, internal tasks, and movie. The functional scans were pre-processed for motion artifacts, manually aligned into the Talairach coordinate system, detrended (removing linear trends in the&lt;br /&gt;
baseline activation) and smoothed (8mm kernel).&lt;br /&gt;
&lt;br /&gt;
Fig. 1 shows the 2-system partition extracted in each subject independently&lt;br /&gt;
of all others. It also displays the boundaries of the intrinsic system determined&lt;br /&gt;
through the traditional seed selection, showing good agreement between the two&lt;br /&gt;
partitions. Fig. 2 presents the results of further clustering the stimulus-driven cluster into two clusters independently for each subject. &lt;br /&gt;
&lt;br /&gt;
&amp;lt;table&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt; &amp;lt;th&amp;gt; '''Fig 1. 2-System Parcelation. Results for all 7 subjects.''' &amp;lt;th&amp;gt; '''Fig 2. 3-System Parcelation. Results for all 7 subjects.''' &lt;br /&gt;
&amp;lt;tr&amp;gt; &amp;lt;td align=&amp;quot;center&amp;quot;&amp;gt; &lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation2_shb1_4.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation2_shb5_6.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation2_shb7.png |400px]]&lt;br /&gt;
&amp;lt;td align=&amp;quot;center&amp;quot;&amp;gt;&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb1_3.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb4_5.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb6.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb7.png |400px]]&lt;br /&gt;
&amp;lt;/table&amp;gt;&lt;br /&gt;
&lt;br /&gt;
Fig.3 presents the group average of the subject-specific 2-system maps. Color shading shows the proportion of subjects whose clustering agreed with the majority label. Fig. 4 shows the group average of a further parcelation of the intrinsic system, i.e., one of two clusters associated with the non-stimulus-driven regions. In order to present a validation of the method, we compare these results with the conventional scheme for detection of visually responsive areas. In Fig. 5, color shows the statistical parametric map while solid lines indicate the boundaries of the visual system obtained through clustering. The result illustrate the agreement between the two methods.&lt;br /&gt;
&lt;br /&gt;
&amp;lt;table&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&amp;lt;th&amp;gt; '''Fig 3. 2-System Parcellation. Group-wise result.'''&lt;br /&gt;
&amp;lt;tr&amp;gt; &amp;lt;td align=&amp;quot;center&amp;quot;&amp;gt;&lt;br /&gt;
{|&lt;br /&gt;
|+ &lt;br /&gt;
|valign=&amp;quot;top&amp;quot;|[[Image:mit_fmri_clustering_parcellation2_xsub.png |thumb|700px]]&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/table&amp;gt;&lt;br /&gt;
&lt;br /&gt;
{|&lt;br /&gt;
|+ '''Fig 4. Validation: Parcelation of the intrinsic system.'''&lt;br /&gt;
|valign=&amp;quot;top&amp;quot;|[[Image:mit_fmri_clustering_intrinsicsystem.png |thumb|650px]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
{|&lt;br /&gt;
|+ '''Fig 5. Validation: Visual system.'''&lt;br /&gt;
|valign=&amp;quot;top&amp;quot;|[[Image:mit_fmri_clustering_validation.png |thumb|1150px]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''' ''Clustering Study of Domain Specificity in High Level Visual Cortex'' '''&lt;br /&gt;
&lt;br /&gt;
As a more specific application of clustering model-based algorithms, we are currently investigating devising clustering algorithms for detection of functional connectivity in high-level visual cortex. It is suggested that there are regions in the visual cortex with high selectivity to certain categories of visual stimuli. Currently, the conventional method for detection of these methods is based on statistical tests comparing response of each voxel in the brain to different visual categories to see if it shows considerably higher activation to one category. For example, the well-known FFA (Fusiform Face Area) is the set of voxels which show high activation to faces when compared to objects. We are working on using the clustering the visual cortex as a means to make this analysis automatic and further discover new structures in the high-level visual cortex.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''' ''Comparison of Data-Driven Analysis Methods for Identiﬁcation of Functional Connectivity in fMRI'' '''&lt;br /&gt;
&lt;br /&gt;
Although ICA and clustering rely on very diﬀerent assumptions on the underlying distributions, they produce surprisingly similar results for signals with large variation. Our main goal is to evaluate and compare the performance of ICA and clustering based on Gaussian mixture model (GMM) for identiﬁcation of functional connectivity. Using the synthetic data with artiﬁcial activations and artifacts under various levels of length of the time course and signal-to-noise ratio of the data, we compare both spatial maps and their associated time courses estimated by ICA and GMM to each other and to the ground truth. We choose the number of sources via the model selection scheme, and compare all of the resulting components of GMM and ICA, not just the task-related components, after we match them component-wise using the Hungarian algorithm. This comparison scheme is veriﬁed in a high level visual cortex fMRI study. We ﬁnd that ICA requires a smaller number of total components to extract the task-related components, but also needs a large number of total components to describe the entire data. We are currently applying ICA and clustering methods to connectivity analysis of schizophrenia patients.&lt;br /&gt;
&lt;br /&gt;
= Key Investigators =&lt;br /&gt;
&lt;br /&gt;
* MIT Algorithms: Danial Lashkari, Y. Bryce Kim, Polina Golland, Nancy Kanwisher&lt;br /&gt;
&lt;br /&gt;
= Publications =&lt;br /&gt;
&lt;br /&gt;
''In print''&lt;br /&gt;
&lt;br /&gt;
* [http://www.na-mic.org/pages/Special:Publications?text=fMRI+Clustering&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;
''In press''&lt;br /&gt;
&lt;br /&gt;
* D. Lashkari, P. Golland. Convex Clustering with Exemplar-Based Models. In NIPS: Advances in Neural Information Processing Systems, 2007.&lt;br /&gt;
&lt;br /&gt;
[[Category:fMRI]]&lt;/div&gt;</summary>
		<author><name>Ybkim</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:fMRIClustering&amp;diff=24713</id>
		<title>Projects:fMRIClustering</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:fMRIClustering&amp;diff=24713"/>
		<updated>2008-05-16T20:43:09Z</updated>

		<summary type="html">&lt;p&gt;Ybkim: /* Description */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Back to [[NA-MIC_Internal_Collaborations:fMRIAnalysis|NA-MIC Collaborations]], [[Algorithm:MIT|MIT Algorithms]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
&lt;br /&gt;
= fMRI Clustering =&lt;br /&gt;
&lt;br /&gt;
One of the major goals in analysis of fMRI data is the detection of networks in the brain with similar functional behavior. A wide variety of methods  including hypothesis-driven statistical tests, unsupervised learning methods such as PCA and ICA, and different clustering algorithms have been employed to find these networks. This project aims to particularly study application of model-based clustering algorithms in identification of functional connectivity in the brain. &lt;br /&gt;
&lt;br /&gt;
= Description =&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
'''''Generative Model for Functional Connectivity'''''&lt;br /&gt;
&lt;br /&gt;
In the classical functional connectivity analysis, networks of interest are&lt;br /&gt;
defined based on correlation with the mean time course of a user-selected&lt;br /&gt;
`seed' region. Further, the user has to also specify a subject-specific threshold at which correlation&lt;br /&gt;
values are deemed significant. In this project, we simultaneously estimate the optimal&lt;br /&gt;
representative time courses that summarize the fMRI data well and&lt;br /&gt;
the partition of the volume into a set of disjoint regions that are best&lt;br /&gt;
explained by these representative time courses. This approach to functional connectivity analysis offers two&lt;br /&gt;
advantages. First, is removes the sensitivity of the analysis to the details&lt;br /&gt;
of the seed selection. Second, it substantially simplifies group analysis&lt;br /&gt;
by eliminating the need for the subject-specific threshold. Our experimental results indicate that&lt;br /&gt;
the functional segmentation provides a robust, anatomically meaningful&lt;br /&gt;
and consistent model for functional connectivity in fMRI.&lt;br /&gt;
&lt;br /&gt;
We formulate the problem of characterizing connectivity as a partition of voxels into subsets that are well characterized by a certain number of representative hypotheses, or time courses, based on the similarity of their time courses to each hypothesis. We model the fMRI signal at each voxel as generated by a mixture of Gaussian distributions whose centers are the desired representative time courses. Using the EM algorithm to solve the corresponding model-fitting problem, we alternatively estimate the representative time courses and cluster assignments to improve our random initialization. &lt;br /&gt;
&lt;br /&gt;
''' ''Experimental Results'' '''&lt;br /&gt;
&lt;br /&gt;
We used data from 7 subjects with a diverse set of visual experiments including localizer, morphing, rest, internal tasks, and movie. The functional scans were pre-processed for motion artifacts, manually aligned into the Talairach coordinate system, detrended (removing linear trends in the&lt;br /&gt;
baseline activation) and smoothed (8mm kernel).&lt;br /&gt;
&lt;br /&gt;
Fig. 1 shows the 2-system partition extracted in each subject independently&lt;br /&gt;
of all others. It also displays the boundaries of the intrinsic system determined&lt;br /&gt;
through the traditional seed selection, showing good agreement between the two&lt;br /&gt;
partitions. Fig. 2 presents the results of further clustering the stimulus-driven cluster into two clusters independently for each subject. &lt;br /&gt;
&lt;br /&gt;
&amp;lt;table&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt; &amp;lt;th&amp;gt; '''Fig 1. 2-System Parcelation. Results for all 7 subjects.''' &amp;lt;th&amp;gt; '''Fig 2. 3-System Parcelation. Results for all 7 subjects.''' &lt;br /&gt;
&amp;lt;tr&amp;gt; &amp;lt;td align=&amp;quot;center&amp;quot;&amp;gt; &lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation2_shb1_4.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation2_shb5_6.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation2_shb7.png |400px]]&lt;br /&gt;
&amp;lt;td align=&amp;quot;center&amp;quot;&amp;gt;&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb1_3.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb4_5.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb6.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb7.png |400px]]&lt;br /&gt;
&amp;lt;/table&amp;gt;&lt;br /&gt;
&lt;br /&gt;
Fig.3 presents the group average of the subject-specific 2-system maps. Color shading shows the proportion of subjects whose clustering agreed with the majority label. Fig. 4 shows the group average of a further parcelation of the intrinsic system, i.e., one of two clusters associated with the non-stimulus-driven regions. In order to present a validation of the method, we compare these results with the conventional scheme for detection of visually responsive areas. In Fig. 5, color shows the statistical parametric map while solid lines indicate the boundaries of the visual system obtained through clustering. The result illustrate the agreement between the two methods.&lt;br /&gt;
&lt;br /&gt;
&amp;lt;table&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&amp;lt;th&amp;gt; '''Fig 3. 2-System Parcellation. Group-wise result.'''&lt;br /&gt;
&amp;lt;tr&amp;gt; &amp;lt;td align=&amp;quot;center&amp;quot;&amp;gt;&lt;br /&gt;
{|&lt;br /&gt;
|+ &lt;br /&gt;
|valign=&amp;quot;top&amp;quot;|[[Image:mit_fmri_clustering_parcellation2_xsub.png |thumb|700px]]&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/table&amp;gt;&lt;br /&gt;
&lt;br /&gt;
{|&lt;br /&gt;
|+ '''Fig 4. Validation: Parcelation of the intrinsic system.'''&lt;br /&gt;
|valign=&amp;quot;top&amp;quot;|[[Image:mit_fmri_clustering_intrinsicsystem.png |thumb|650px]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
{|&lt;br /&gt;
|+ '''Fig 5. Validation: Visual system.'''&lt;br /&gt;
|valign=&amp;quot;top&amp;quot;|[[Image:mit_fmri_clustering_validation.png |thumb|1150px]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''' ''Clustering Study of Domain Specificity in High Level Visual Cortex'' '''&lt;br /&gt;
&lt;br /&gt;
As a more specific application of clustering model-based algorithms, we are currently investigating devising clustering algorithms for detection of functional connectivity in high-level visual cortex. It is suggested that there are regions in the visual cortex with high selectivity to certain categories of visual stimuli. Currently, the conventional method for detection of these methods is based on statistical tests comparing response of each voxel in the brain to different visual categories to see if it shows considerably higher activation to one category. For example, the well-known FFA (Fusiform Face Area) is the set of voxels which show high activation to faces when compared to objects. We are working on using the clustering the visual cortex as a means to make this analysis automatic and further discover new structures in the high-level visual cortex.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''' ''Comparison of Data-Driven Analysis Methods for Identiﬁcation of Functional Connectivity in fMRI'' '''&lt;br /&gt;
&lt;br /&gt;
Although ICA and clustering rely on very diﬀerent assumptions on the underlying distributions, they produce surprisingly similar results for signals with large variation. Our main goal is to evaluate and compare the performance of ICA and clustering based on Gaussian mixture model (GMM) for identiﬁcation of functional connectivity. Using the synthetic data with artiﬁcial activations and artifacts under various levels of length of the time course and signal-to-noise ratio of the data, we compare both spatial maps and their associated time courses estimated by ICA and GMM to each other and to the ground truth. We choose the number of sources via the model selection scheme. We compare all of the resulting components of GMM and ICA, not just the task-related components, after we match them component-wise using the Hungarian algorithm. This comparison scheme is veriﬁed in a high level visual cortex fMRI study. Figure 6 showsWe ﬁnd that ICA requires a smaller number of total components to extract the task-related components, but also needs a large number of total components to describe the entire data. We are currently applying ICA and clustering methods to connectivity analysis of schizophrenia patients.&lt;br /&gt;
&lt;br /&gt;
= Key Investigators =&lt;br /&gt;
&lt;br /&gt;
* MIT Algorithms: Danial Lashkari, Y. Bryce Kim, Polina Golland, Nancy Kanwisher&lt;br /&gt;
&lt;br /&gt;
= Publications =&lt;br /&gt;
&lt;br /&gt;
''In print''&lt;br /&gt;
&lt;br /&gt;
* [http://www.na-mic.org/pages/Special:Publications?text=fMRI+Clustering&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;
''In press''&lt;br /&gt;
&lt;br /&gt;
* D. Lashkari, P. Golland. Convex Clustering with Exemplar-Based Models. In NIPS: Advances in Neural Information Processing Systems, 2007.&lt;br /&gt;
&lt;br /&gt;
[[Category:fMRI]]&lt;/div&gt;</summary>
		<author><name>Ybkim</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:fMRIClustering&amp;diff=24708</id>
		<title>Projects:fMRIClustering</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:fMRIClustering&amp;diff=24708"/>
		<updated>2008-05-16T20:36:13Z</updated>

		<summary type="html">&lt;p&gt;Ybkim: /* Description */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Back to [[NA-MIC_Internal_Collaborations:fMRIAnalysis|NA-MIC Collaborations]], [[Algorithm:MIT|MIT Algorithms]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
&lt;br /&gt;
= fMRI Clustering =&lt;br /&gt;
&lt;br /&gt;
One of the major goals in analysis of fMRI data is the detection of networks in the brain with similar functional behavior. A wide variety of methods  including hypothesis-driven statistical tests, unsupervised learning methods such as PCA and ICA, and different clustering algorithms have been employed to find these networks. This project aims to particularly study application of model-based clustering algorithms in identification of functional connectivity in the brain. &lt;br /&gt;
&lt;br /&gt;
= Description =&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
'''''Generative Model for Functional Connectivity'''''&lt;br /&gt;
&lt;br /&gt;
In the classical functional connectivity analysis, networks of interest are&lt;br /&gt;
defined based on correlation with the mean time course of a user-selected&lt;br /&gt;
`seed' region. Further, the user has to also specify a subject-specific threshold at which correlation&lt;br /&gt;
values are deemed significant. In this project, we simultaneously estimate the optimal&lt;br /&gt;
representative time courses that summarize the fMRI data well and&lt;br /&gt;
the partition of the volume into a set of disjoint regions that are best&lt;br /&gt;
explained by these representative time courses. This approach to functional connectivity analysis offers two&lt;br /&gt;
advantages. First, is removes the sensitivity of the analysis to the details&lt;br /&gt;
of the seed selection. Second, it substantially simplifies group analysis&lt;br /&gt;
by eliminating the need for the subject-specific threshold. Our experimental results indicate that&lt;br /&gt;
the functional segmentation provides a robust, anatomically meaningful&lt;br /&gt;
and consistent model for functional connectivity in fMRI.&lt;br /&gt;
&lt;br /&gt;
We formulate the problem of characterizing connectivity as a partition of voxels into subsets that are well characterized by a certain number of representative hypotheses, or time courses, based on the similarity of their time courses to each hypothesis. We model the fMRI signal at each voxel as generated by a mixture of Gaussian distributions whose centers are the desired representative time courses. Using the EM algorithm to solve the corresponding model-fitting problem, we alternatively estimate the representative time courses and cluster assignments to improve our random initialization. &lt;br /&gt;
&lt;br /&gt;
''' ''Experimental Results'' '''&lt;br /&gt;
&lt;br /&gt;
We used data from 7 subjects with a diverse set of visual experiments including localizer, morphing, rest, internal tasks, and movie. The functional scans were pre-processed for motion artifacts, manually aligned into the Talairach coordinate system, detrended (removing linear trends in the&lt;br /&gt;
baseline activation) and smoothed (8mm kernel).&lt;br /&gt;
&lt;br /&gt;
Fig. 1 shows the 2-system partition extracted in each subject independently&lt;br /&gt;
of all others. It also displays the boundaries of the intrinsic system determined&lt;br /&gt;
through the traditional seed selection, showing good agreement between the two&lt;br /&gt;
partitions. Fig. 2 presents the results of further clustering the stimulus-driven cluster into two clusters independently for each subject. &lt;br /&gt;
&lt;br /&gt;
&amp;lt;table&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt; &amp;lt;th&amp;gt; '''Fig 1. 2-System Parcelation. Results for all 7 subjects.''' &amp;lt;th&amp;gt; '''Fig 2. 3-System Parcelation. Results for all 7 subjects.''' &lt;br /&gt;
&amp;lt;tr&amp;gt; &amp;lt;td align=&amp;quot;center&amp;quot;&amp;gt; &lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation2_shb1_4.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation2_shb5_6.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation2_shb7.png |400px]]&lt;br /&gt;
&amp;lt;td align=&amp;quot;center&amp;quot;&amp;gt;&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb1_3.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb4_5.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb6.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb7.png |400px]]&lt;br /&gt;
&amp;lt;/table&amp;gt;&lt;br /&gt;
&lt;br /&gt;
Fig.3 presents the group average of the subject-specific 2-system maps. Color shading shows the proportion of subjects whose clustering agreed with the majority label. Fig. 4 shows the group average of a further parcelation of the intrinsic system, i.e., one of two clusters associated with the non-stimulus-driven regions. In order to present a validation of the method, we compare these results with the conventional scheme for detection of visually responsive areas. In Fig. 5, color shows the statistical parametric map while solid lines indicate the boundaries of the visual system obtained through clustering. The result illustrate the agreement between the two methods.&lt;br /&gt;
&lt;br /&gt;
&amp;lt;table&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&amp;lt;th&amp;gt; '''Fig 3. 2-System Parcellation. Group-wise result.'''&lt;br /&gt;
&amp;lt;tr&amp;gt; &amp;lt;td align=&amp;quot;center&amp;quot;&amp;gt;&lt;br /&gt;
{|&lt;br /&gt;
|+ &lt;br /&gt;
|valign=&amp;quot;top&amp;quot;|[[Image:mit_fmri_clustering_parcellation2_xsub.png |thumb|700px]]&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/table&amp;gt;&lt;br /&gt;
&lt;br /&gt;
{|&lt;br /&gt;
|+ '''Fig 4. Validation: Parcelation of the intrinsic system.'''&lt;br /&gt;
|valign=&amp;quot;top&amp;quot;|[[Image:mit_fmri_clustering_intrinsicsystem.png |thumb|650px]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
{|&lt;br /&gt;
|+ '''Fig 5. Validation: Visual system.'''&lt;br /&gt;
|valign=&amp;quot;top&amp;quot;|[[Image:mit_fmri_clustering_validation.png |thumb|1150px]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''' ''Clustering Study of Domain Specificity in High Level Visual Cortex'' '''&lt;br /&gt;
&lt;br /&gt;
As a more specific application of clustering model-based algorithms, we are currently investigating devising clustering algorithms for detection of functional connectivity in high-level visual cortex. It is suggested that there are regions in the visual cortex with high selectivity to certain categories of visual stimuli. Currently, the conventional method for detection of these methods is based on statistical tests comparing response of each voxel in the brain to different visual categories to see if it shows considerably higher activation to one category. For example, the well-known FFA (Fusiform Face Area) is the set of voxels which show high activation to faces when compared to objects. We are working on using the clustering the visual cortex as a means to make this analysis automatic and further discover new structures in the high-level visual cortex.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''' ''Comparison of Data-Driven Analysis Methods for Identiﬁcation of Functional Connectivity in fMRI'' '''&lt;br /&gt;
&lt;br /&gt;
Although ICA and clustering rely on very diﬀerent assumptions on the underlying distributions, they produce surprisingly similar results for signals with large variation. Our main goal is to evaluate and compare the performance of ICA and clustering based on Gaussian mixture model (GMM) for identiﬁcation of functional connectivity. Using the synthetic data with artiﬁcial activations and artifacts under various levels of length of the time course and signal-to-noise ratio of the data, we compare both spatial maps and their associated time courses estimated by ICA and GMM to each other and to the ground truth. We choose the number of sources via the model selection scheme. We compare all of the resulting components of GMM and ICA, not just the task-related components, after we match them component-wise using the Hungarian algorithm. This comparison scheme is veriﬁed in a high level visual cortex fMRI study. We ﬁnd that ICA requires a smaller number of total components to extract the task-related components, but also needs a large number of total components to describe the entire data.&lt;br /&gt;
&lt;br /&gt;
= Key Investigators =&lt;br /&gt;
&lt;br /&gt;
* MIT Algorithms: Danial Lashkari, Y. Bryce Kim, Polina Golland, Nancy Kanwisher&lt;br /&gt;
&lt;br /&gt;
= Publications =&lt;br /&gt;
&lt;br /&gt;
''In print''&lt;br /&gt;
&lt;br /&gt;
* [http://www.na-mic.org/pages/Special:Publications?text=fMRI+Clustering&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;
''In press''&lt;br /&gt;
&lt;br /&gt;
* D. Lashkari, P. Golland. Convex Clustering with Exemplar-Based Models. In NIPS: Advances in Neural Information Processing Systems, 2007.&lt;br /&gt;
&lt;br /&gt;
[[Category:fMRI]]&lt;/div&gt;</summary>
		<author><name>Ybkim</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:fMRIClustering&amp;diff=24707</id>
		<title>Projects:fMRIClustering</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:fMRIClustering&amp;diff=24707"/>
		<updated>2008-05-16T20:35:15Z</updated>

		<summary type="html">&lt;p&gt;Ybkim: /* Description */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Back to [[NA-MIC_Internal_Collaborations:fMRIAnalysis|NA-MIC Collaborations]], [[Algorithm:MIT|MIT Algorithms]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
&lt;br /&gt;
= fMRI Clustering =&lt;br /&gt;
&lt;br /&gt;
One of the major goals in analysis of fMRI data is the detection of networks in the brain with similar functional behavior. A wide variety of methods  including hypothesis-driven statistical tests, unsupervised learning methods such as PCA and ICA, and different clustering algorithms have been employed to find these networks. This project aims to particularly study application of model-based clustering algorithms in identification of functional connectivity in the brain. &lt;br /&gt;
&lt;br /&gt;
= Description =&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
'''''Generative Model for Functional Connectivity'''''&lt;br /&gt;
&lt;br /&gt;
In the classical functional connectivity analysis, networks of interest are&lt;br /&gt;
defined based on correlation with the mean time course of a user-selected&lt;br /&gt;
`seed' region. Further, the user has to also specify a subject-specific threshold at which correlation&lt;br /&gt;
values are deemed significant. In this project, we simultaneously estimate the optimal&lt;br /&gt;
representative time courses that summarize the fMRI data well and&lt;br /&gt;
the partition of the volume into a set of disjoint regions that are best&lt;br /&gt;
explained by these representative time courses. This approach to functional connectivity analysis offers two&lt;br /&gt;
advantages. First, is removes the sensitivity of the analysis to the details&lt;br /&gt;
of the seed selection. Second, it substantially simplifies group analysis&lt;br /&gt;
by eliminating the need for the subject-specific threshold. Our experimental results indicate that&lt;br /&gt;
the functional segmentation provides a robust, anatomically meaningful&lt;br /&gt;
and consistent model for functional connectivity in fMRI.&lt;br /&gt;
&lt;br /&gt;
We formulate the problem of characterizing connectivity as a partition of voxels into subsets that are well characterized by a certain number of representative hypotheses, or time courses, based on the similarity of their time courses to each hypothesis. We model the fMRI signal at each voxel as generated by a mixture of Gaussian distributions whose centers are the desired representative time courses. Using the EM algorithm to solve the corresponding model-fitting problem, we alternatively estimate the representative time courses and cluster assignments to improve our random initialization. &lt;br /&gt;
&lt;br /&gt;
''' ''Experimental Results'' '''&lt;br /&gt;
&lt;br /&gt;
We used data from 7 subjects with a diverse set of visual experiments including localizer, morphing, rest, internal tasks, and movie. The functional scans were pre-processed for motion artifacts, manually aligned into the Talairach coordinate system, detrended (removing linear trends in the&lt;br /&gt;
baseline activation) and smoothed (8mm kernel).&lt;br /&gt;
&lt;br /&gt;
Fig. 1 shows the 2-system partition extracted in each subject independently&lt;br /&gt;
of all others. It also displays the boundaries of the intrinsic system determined&lt;br /&gt;
through the traditional seed selection, showing good agreement between the two&lt;br /&gt;
partitions. Fig. 2 presents the results of further clustering the stimulus-driven cluster into two clusters independently for each subject. &lt;br /&gt;
&lt;br /&gt;
&amp;lt;table&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt; &amp;lt;th&amp;gt; '''Fig 1. 2-System Parcelation. Results for all 7 subjects.''' &amp;lt;th&amp;gt; '''Fig 2. 3-System Parcelation. Results for all 7 subjects.''' &lt;br /&gt;
&amp;lt;tr&amp;gt; &amp;lt;td align=&amp;quot;center&amp;quot;&amp;gt; &lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation2_shb1_4.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation2_shb5_6.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation2_shb7.png |400px]]&lt;br /&gt;
&amp;lt;td align=&amp;quot;center&amp;quot;&amp;gt;&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb1_3.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb4_5.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb6.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb7.png |400px]]&lt;br /&gt;
&amp;lt;/table&amp;gt;&lt;br /&gt;
&lt;br /&gt;
Fig.3 presents the group average of the subject-specific 2-system maps. Color shading shows the proportion of subjects whose clustering agreed with the majority label. Fig. 4 shows the group average of a further parcelation of the intrinsic system, i.e., one of two clusters associated with the non-stimulus-driven regions. In order to present a validation of the method, we compare these results with the conventional scheme for detection of visually responsive areas. In Fig. 5, color shows the statistical parametric map while solid lines indicate the boundaries of the visual system obtained through clustering. The result illustrate the agreement between the two methods.&lt;br /&gt;
&lt;br /&gt;
&amp;lt;table&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&amp;lt;th&amp;gt; '''Fig 3. 2-System Parcellation. Group-wise result.'''&lt;br /&gt;
&amp;lt;tr&amp;gt; &amp;lt;td align=&amp;quot;center&amp;quot;&amp;gt;&lt;br /&gt;
{|&lt;br /&gt;
|+ &lt;br /&gt;
|valign=&amp;quot;top&amp;quot;|[[Image:mit_fmri_clustering_parcellation2_xsub.png |thumb|700px]]&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/table&amp;gt;&lt;br /&gt;
&lt;br /&gt;
{|&lt;br /&gt;
|+ '''Fig 4. Validation: Parcelation of the intrinsic system.'''&lt;br /&gt;
|valign=&amp;quot;top&amp;quot;|[[Image:mit_fmri_clustering_intrinsicsystem.png |thumb|650px]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
{|&lt;br /&gt;
|+ '''Fig 5. Validation: Visual system.'''&lt;br /&gt;
|valign=&amp;quot;top&amp;quot;|[[Image:mit_fmri_clustering_validation.png |thumb|1150px]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''' ''Clustering Study of Domain Specificity in High Level Visual Cortex'' '''&lt;br /&gt;
&lt;br /&gt;
As a more specific application of clustering model-based algorithms, we are currently investigating devising clustering algorithms for detection of functional connectivity in high-level visual cortex. It is suggested that there are regions in the visual cortex with high selectivity to certain categories of visual stimuli. Currently, the conventional method for detection of these methods is based on statistical tests comparing response of each voxel in the brain to different visual categories to see if it shows considerably higher activation to one category. For example, the well-known FFA (Fusiform Face Area) is the set of voxels which show high activation to faces when compared to objects. We are working on using the clustering the visual cortex as a means to make this analysis automatic and further discover new structures in the high-level visual cortex.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''' ''Comparison of Data-Driven Analysis Methods for Identiﬁcation of Functional Connectivity in fMRI'' '''&lt;br /&gt;
&lt;br /&gt;
Although ICA and clustering rely on very diﬀerent assumptions on the underlying distributions, they produce surprisingly similar results for signals with large variation. Our main goal is to evaluate and compare the performance of ICA and clustering based on Gaussian mixture model (GMM) for identiﬁcation of functional connectivity. Using the synthetic data with artiﬁcial activations and artifacts under various levels of length of the time course and signal-to-noise ratio (SNR) of the data, we compare both spatial maps and their associated time courses estimated by ICA and GMM to each other and to the ground truth. We choose the number of sources via the model selection scheme. We compare all of the resulting components of GMM and ICA, not just the task-related components, after we match them component-wise using the Hungarian algorithm. This comparison scheme is veriﬁed in a high level visual cortex fMRI study. We ﬁnd that ICA requires a smaller number of total components to extract the task-related components, but also needs a large number of total components to describe the entire data.&lt;br /&gt;
&lt;br /&gt;
= Key Investigators =&lt;br /&gt;
&lt;br /&gt;
* MIT Algorithms: Danial Lashkari, Y. Bryce Kim, Polina Golland, Nancy Kanwisher&lt;br /&gt;
&lt;br /&gt;
= Publications =&lt;br /&gt;
&lt;br /&gt;
''In print''&lt;br /&gt;
&lt;br /&gt;
* [http://www.na-mic.org/pages/Special:Publications?text=fMRI+Clustering&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;
''In press''&lt;br /&gt;
&lt;br /&gt;
* D. Lashkari, P. Golland. Convex Clustering with Exemplar-Based Models. In NIPS: Advances in Neural Information Processing Systems, 2007.&lt;br /&gt;
&lt;br /&gt;
[[Category:fMRI]]&lt;/div&gt;</summary>
		<author><name>Ybkim</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:fMRIClustering&amp;diff=24703</id>
		<title>Projects:fMRIClustering</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:fMRIClustering&amp;diff=24703"/>
		<updated>2008-05-16T20:29:36Z</updated>

		<summary type="html">&lt;p&gt;Ybkim: /* Description */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Back to [[NA-MIC_Internal_Collaborations:fMRIAnalysis|NA-MIC Collaborations]], [[Algorithm:MIT|MIT Algorithms]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
&lt;br /&gt;
= fMRI Clustering =&lt;br /&gt;
&lt;br /&gt;
One of the major goals in analysis of fMRI data is the detection of networks in the brain with similar functional behavior. A wide variety of methods  including hypothesis-driven statistical tests, unsupervised learning methods such as PCA and ICA, and different clustering algorithms have been employed to find these networks. This project aims to particularly study application of model-based clustering algorithms in identification of functional connectivity in the brain. &lt;br /&gt;
&lt;br /&gt;
= Description =&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
'''''Generative Model for Functional Connectivity'''''&lt;br /&gt;
&lt;br /&gt;
In the classical functional connectivity analysis, networks of interest are&lt;br /&gt;
defined based on correlation with the mean time course of a user-selected&lt;br /&gt;
`seed' region. Further, the user has to also specify a subject-specific threshold at which correlation&lt;br /&gt;
values are deemed significant. In this project, we simultaneously estimate the optimal&lt;br /&gt;
representative time courses that summarize the fMRI data well and&lt;br /&gt;
the partition of the volume into a set of disjoint regions that are best&lt;br /&gt;
explained by these representative time courses. This approach to functional connectivity analysis offers two&lt;br /&gt;
advantages. First, is removes the sensitivity of the analysis to the details&lt;br /&gt;
of the seed selection. Second, it substantially simplifies group analysis&lt;br /&gt;
by eliminating the need for the subject-specific threshold. Our experimental results indicate that&lt;br /&gt;
the functional segmentation provides a robust, anatomically meaningful&lt;br /&gt;
and consistent model for functional connectivity in fMRI.&lt;br /&gt;
&lt;br /&gt;
We formulate the problem of characterizing connectivity as a partition of voxels into subsets that are well characterized by a certain number of representative hypotheses, or time courses, based on the similarity of their time courses to each hypothesis. We model the fMRI signal at each voxel as generated by a mixture of Gaussian distributions whose centers are the desired representative time courses. Using the EM algorithm to solve the corresponding model-fitting problem, we alternatively estimate the representative time courses and cluster assignments to improve our random initialization. &lt;br /&gt;
&lt;br /&gt;
''' ''Experimental Results'' '''&lt;br /&gt;
&lt;br /&gt;
We used data from 7 subjects with a diverse set of visual experiments including localizer, morphing, rest, internal tasks, and movie. The functional scans were pre-processed for motion artifacts, manually aligned into the Talairach coordinate system, detrended (removing linear trends in the&lt;br /&gt;
baseline activation) and smoothed (8mm kernel).&lt;br /&gt;
&lt;br /&gt;
Fig. 1 shows the 2-system partition extracted in each subject independently&lt;br /&gt;
of all others. It also displays the boundaries of the intrinsic system determined&lt;br /&gt;
through the traditional seed selection, showing good agreement between the two&lt;br /&gt;
partitions. Fig. 2 presents the results of further clustering the stimulus-driven cluster into two clusters independently for each subject. &lt;br /&gt;
&lt;br /&gt;
&amp;lt;table&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt; &amp;lt;th&amp;gt; '''Fig 1. 2-System Parcelation. Results for all 7 subjects.''' &amp;lt;th&amp;gt; '''Fig 2. 3-System Parcelation. Results for all 7 subjects.''' &lt;br /&gt;
&amp;lt;tr&amp;gt; &amp;lt;td align=&amp;quot;center&amp;quot;&amp;gt; &lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation2_shb1_4.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation2_shb5_6.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation2_shb7.png |400px]]&lt;br /&gt;
&amp;lt;td align=&amp;quot;center&amp;quot;&amp;gt;&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb1_3.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb4_5.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb6.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb7.png |400px]]&lt;br /&gt;
&amp;lt;/table&amp;gt;&lt;br /&gt;
&lt;br /&gt;
Fig.3 presents the group average of the subject-specific 2-system maps. Color shading shows the proportion of subjects whose clustering agreed with the majority label. Fig. 4 shows the group average of a further parcelation of the intrinsic system, i.e., one of two clusters associated with the non-stimulus-driven regions. In order to present a validation of the method, we compare these results with the conventional scheme for detection of visually responsive areas. In Fig. 5, color shows the statistical parametric map while solid lines indicate the boundaries of the visual system obtained through clustering. The result illustrate the agreement between the two methods.&lt;br /&gt;
&lt;br /&gt;
&amp;lt;table&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&amp;lt;th&amp;gt; '''Fig 3. 2-System Parcellation. Group-wise result.'''&lt;br /&gt;
&amp;lt;tr&amp;gt; &amp;lt;td align=&amp;quot;center&amp;quot;&amp;gt;&lt;br /&gt;
{|&lt;br /&gt;
|+ &lt;br /&gt;
|valign=&amp;quot;top&amp;quot;|[[Image:mit_fmri_clustering_parcellation2_xsub.png |thumb|700px]]&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/table&amp;gt;&lt;br /&gt;
&lt;br /&gt;
{|&lt;br /&gt;
|+ '''Fig 4. Validation: Parcelation of the intrinsic system.'''&lt;br /&gt;
|valign=&amp;quot;top&amp;quot;|[[Image:mit_fmri_clustering_intrinsicsystem.png |thumb|650px]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
{|&lt;br /&gt;
|+ '''Fig 5. Validation: Visual system.'''&lt;br /&gt;
|valign=&amp;quot;top&amp;quot;|[[Image:mit_fmri_clustering_validation.png |thumb|1150px]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''' ''Clustering Study of Domain Specificity in High Level Visual Cortex'' '''&lt;br /&gt;
&lt;br /&gt;
As a more specific application of clustering model-based algorithms, we are currently investigating devising clustering algorithms for detection of functional connectivity in high-level visual cortex. It is suggested that there are regions in the visual cortex with high selectivity to certain categories of visual stimuli. Currently, the conventional method for detection of these methods is based on statistical tests comparing response of each voxel in the brain to different visual categories to see if it shows considerably higher activation to one category. For example, the well-known FFA (Fusiform Face Area) is the set of voxels which show high activation to faces when compared to objects. We are working on using the clustering the visual cortex as a means to make this analysis automatic and further discover new structures in the high-level visual cortex.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''' ''Comparison of Data-Driven Analysis Methods for Identiﬁcation of Functional Connectivity in fMRI'' '''&lt;br /&gt;
&lt;br /&gt;
Although ICA and clustering rely on very diﬀerent assumptions on the underlying distributions, they produce surprisingly similar results for signals with large variation. Our main goal is to evaluate and compare the performance of ICA and clustering based on Gaussian mixture model (GMM) for identiﬁcation of functional connectivity. Using the synthetic data with artiﬁcial activations and artifacts under various levels of length of the time course and signal-to-noise ratio (SNR) of the data, both spatial maps and their associated time courses estimated by ICA and GMM are compared to each other and to the ground truth. The number of sources is chosen via the model selection scheme and all selected components are compared, not just the task-related components. This comparison scheme is veriﬁed in a high level visual cortex fMRI study. We ﬁnd that ICA requires a smaller number of total components to extract the task-related components, but also needs a large number of total components to describe the entire data.&lt;br /&gt;
&lt;br /&gt;
= Key Investigators =&lt;br /&gt;
&lt;br /&gt;
* MIT Algorithms: Danial Lashkari, Y. Bryce Kim, Polina Golland, Nancy Kanwisher&lt;br /&gt;
&lt;br /&gt;
= Publications =&lt;br /&gt;
&lt;br /&gt;
''In print''&lt;br /&gt;
&lt;br /&gt;
* [http://www.na-mic.org/pages/Special:Publications?text=fMRI+Clustering&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;
''In press''&lt;br /&gt;
&lt;br /&gt;
* D. Lashkari, P. Golland. Convex Clustering with Exemplar-Based Models. In NIPS: Advances in Neural Information Processing Systems, 2007.&lt;br /&gt;
&lt;br /&gt;
[[Category:fMRI]]&lt;/div&gt;</summary>
		<author><name>Ybkim</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:fMRIClustering&amp;diff=24699</id>
		<title>Projects:fMRIClustering</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:fMRIClustering&amp;diff=24699"/>
		<updated>2008-05-16T20:25:16Z</updated>

		<summary type="html">&lt;p&gt;Ybkim: /* Description */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Back to [[NA-MIC_Internal_Collaborations:fMRIAnalysis|NA-MIC Collaborations]], [[Algorithm:MIT|MIT Algorithms]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
&lt;br /&gt;
= fMRI Clustering =&lt;br /&gt;
&lt;br /&gt;
One of the major goals in analysis of fMRI data is the detection of networks in the brain with similar functional behavior. A wide variety of methods  including hypothesis-driven statistical tests, unsupervised learning methods such as PCA and ICA, and different clustering algorithms have been employed to find these networks. This project aims to particularly study application of model-based clustering algorithms in identification of functional connectivity in the brain. &lt;br /&gt;
&lt;br /&gt;
= Description =&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
'''''Generative Model for Functional Connectivity'''''&lt;br /&gt;
&lt;br /&gt;
In the classical functional connectivity analysis, networks of interest are&lt;br /&gt;
defined based on correlation with the mean time course of a user-selected&lt;br /&gt;
`seed' region. Further, the user has to also specify a subject-specific threshold at which correlation&lt;br /&gt;
values are deemed significant. In this project, we simultaneously estimate the optimal&lt;br /&gt;
representative time courses that summarize the fMRI data well and&lt;br /&gt;
the partition of the volume into a set of disjoint regions that are best&lt;br /&gt;
explained by these representative time courses. This approach to functional connectivity analysis offers two&lt;br /&gt;
advantages. First, is removes the sensitivity of the analysis to the details&lt;br /&gt;
of the seed selection. Second, it substantially simplifies group analysis&lt;br /&gt;
by eliminating the need for the subject-specific threshold. Our experimental results indicate that&lt;br /&gt;
the functional segmentation provides a robust, anatomically meaningful&lt;br /&gt;
and consistent model for functional connectivity in fMRI.&lt;br /&gt;
&lt;br /&gt;
We formulate the problem of characterizing connectivity as a partition of voxels into subsets that are well characterized by a certain number of representative hypotheses, or time courses, based on the similarity of their time courses to each hypothesis. We model the fMRI signal at each voxel as generated by a mixture of Gaussian distributions whose centers are the desired representative time courses. Using the EM algorithm to solve the corresponding model-fitting problem, we alternatively estimate the representative time courses and cluster assignments to improve our random initialization. &lt;br /&gt;
&lt;br /&gt;
''' ''Experimental Results'' '''&lt;br /&gt;
&lt;br /&gt;
We used data from 7 subjects with a diverse set of visual experiments including localizer, morphing, rest, internal tasks, and movie. The functional scans were pre-processed for motion artifacts, manually aligned into the Talairach coordinate system, detrended (removing linear trends in the&lt;br /&gt;
baseline activation) and smoothed (8mm kernel).&lt;br /&gt;
&lt;br /&gt;
Fig. 1 shows the 2-system partition extracted in each subject independently&lt;br /&gt;
of all others. It also displays the boundaries of the intrinsic system determined&lt;br /&gt;
through the traditional seed selection, showing good agreement between the two&lt;br /&gt;
partitions. Fig. 2 presents the results of further clustering the stimulus-driven cluster into two clusters independently for each subject. &lt;br /&gt;
&lt;br /&gt;
&amp;lt;table&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt; &amp;lt;th&amp;gt; '''Fig 1. 2-System Parcelation. Results for all 7 subjects.''' &amp;lt;th&amp;gt; '''Fig 2. 3-System Parcelation. Results for all 7 subjects.''' &lt;br /&gt;
&amp;lt;tr&amp;gt; &amp;lt;td align=&amp;quot;center&amp;quot;&amp;gt; &lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation2_shb1_4.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation2_shb5_6.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation2_shb7.png |400px]]&lt;br /&gt;
&amp;lt;td align=&amp;quot;center&amp;quot;&amp;gt;&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb1_3.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb4_5.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb6.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb7.png |400px]]&lt;br /&gt;
&amp;lt;/table&amp;gt;&lt;br /&gt;
&lt;br /&gt;
Fig.3 presents the group average of the subject-specific 2-system maps. Color shading shows the proportion of subjects whose clustering agreed with the majority label. Fig. 4 shows the group average of a further parcelation of the intrinsic system, i.e., one of two clusters associated with the non-stimulus-driven regions. In order to present a validation of the method, we compare these results with the conventional scheme for detection of visually responsive areas. In Fig. 5, color shows the statistical parametric map while solid lines indicate the boundaries of the visual system obtained through clustering. The result illustrate the agreement between the two methods.&lt;br /&gt;
&lt;br /&gt;
&amp;lt;table&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&amp;lt;th&amp;gt; '''Fig 3. 2-System Parcellation. Group-wise result.'''&lt;br /&gt;
&amp;lt;tr&amp;gt; &amp;lt;td align=&amp;quot;center&amp;quot;&amp;gt;&lt;br /&gt;
{|&lt;br /&gt;
|+ &lt;br /&gt;
|valign=&amp;quot;top&amp;quot;|[[Image:mit_fmri_clustering_parcellation2_xsub.png |thumb|700px]]&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/table&amp;gt;&lt;br /&gt;
&lt;br /&gt;
{|&lt;br /&gt;
|+ '''Fig 4. Validation: Parcelation of the intrinsic system.'''&lt;br /&gt;
|valign=&amp;quot;top&amp;quot;|[[Image:mit_fmri_clustering_intrinsicsystem.png |thumb|650px]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
{|&lt;br /&gt;
|+ '''Fig 5. Validation: Visual system.'''&lt;br /&gt;
|valign=&amp;quot;top&amp;quot;|[[Image:mit_fmri_clustering_validation.png |thumb|1150px]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''' ''Clustering Study of Domain Specificity in High Level Visual Cortex'' '''&lt;br /&gt;
&lt;br /&gt;
As a more specific application of clustering model-based algorithms, we are currently investigating devising clustering algorithms for detection of functional connectivity in high-level visual cortex. It is suggested that there are regions in the visual cortex with high selectivity to certain categories of visual stimuli. Currently, the conventional method for detection of these methods is based on statistical tests comparing response of each voxel in the brain to different visual categories to see if it shows considerably higher activation to one category. For example, the well-known FFA (Fusiform Face Area) is the set of voxels which show high activation to faces when compared to objects. We are working on using the clustering the visual cortex as a means to make this analysis automatic and further discover new structures in the high-level visual cortex.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''' ''Comparison of Data-Driven Analysis Methods for Identiﬁcation of Functional Connectivity in fMRI'' '''&lt;br /&gt;
&lt;br /&gt;
Although ICA and clustering rely on very diﬀerent assumptions on the underlying distributions, they produce surprisingly similar results for signals with large variation. Our main goal is to evaluate and compare the performance of ICA and clustering based on Gaussian mixture model (GMM) for identiﬁcation of functional connectivity. Using the synthetic data with artiﬁcial activations and artifacts under two experimental conditions (length of the time course and signal-to-noise ratio (SNR) of the data), both spatial maps and their associated time courses estimated by ICA and GMM are compared to each other and to the ground truth. The number of sources is chosen via the model selection scheme and all selected components are compared, not just the task-related components. This comparison scheme is veriﬁed in a real visual recognition fMRI study. We ﬁnd that ICA requires a smaller number of total components to extract the task-related components, but also needs a large number of total components to describe the entire data, whereas the diﬀerence between those values is small for GMM.&lt;br /&gt;
&lt;br /&gt;
= Key Investigators =&lt;br /&gt;
&lt;br /&gt;
* MIT Algorithms: Danial Lashkari, Y. Bryce Kim, Polina Golland, Nancy Kanwisher&lt;br /&gt;
&lt;br /&gt;
= Publications =&lt;br /&gt;
&lt;br /&gt;
''In print''&lt;br /&gt;
&lt;br /&gt;
* [http://www.na-mic.org/pages/Special:Publications?text=fMRI+Clustering&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;
''In press''&lt;br /&gt;
&lt;br /&gt;
* D. Lashkari, P. Golland. Convex Clustering with Exemplar-Based Models. In NIPS: Advances in Neural Information Processing Systems, 2007.&lt;br /&gt;
&lt;br /&gt;
[[Category:fMRI]]&lt;/div&gt;</summary>
		<author><name>Ybkim</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:fMRIClustering&amp;diff=24693</id>
		<title>Projects:fMRIClustering</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:fMRIClustering&amp;diff=24693"/>
		<updated>2008-05-16T20:22:53Z</updated>

		<summary type="html">&lt;p&gt;Ybkim: /* Description */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Back to [[NA-MIC_Internal_Collaborations:fMRIAnalysis|NA-MIC Collaborations]], [[Algorithm:MIT|MIT Algorithms]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
&lt;br /&gt;
= fMRI Clustering =&lt;br /&gt;
&lt;br /&gt;
One of the major goals in analysis of fMRI data is the detection of networks in the brain with similar functional behavior. A wide variety of methods  including hypothesis-driven statistical tests, unsupervised learning methods such as PCA and ICA, and different clustering algorithms have been employed to find these networks. This project aims to particularly study application of model-based clustering algorithms in identification of functional connectivity in the brain. &lt;br /&gt;
&lt;br /&gt;
= Description =&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
'''''Generative Model for Functional Connectivity'''''&lt;br /&gt;
&lt;br /&gt;
In the classical functional connectivity analysis, networks of interest are&lt;br /&gt;
defined based on correlation with the mean time course of a user-selected&lt;br /&gt;
`seed' region. Further, the user has to also specify a subject-specific threshold at which correlation&lt;br /&gt;
values are deemed significant. In this project, we simultaneously estimate the optimal&lt;br /&gt;
representative time courses that summarize the fMRI data well and&lt;br /&gt;
the partition of the volume into a set of disjoint regions that are best&lt;br /&gt;
explained by these representative time courses. This approach to functional connectivity analysis offers two&lt;br /&gt;
advantages. First, is removes the sensitivity of the analysis to the details&lt;br /&gt;
of the seed selection. Second, it substantially simplifies group analysis&lt;br /&gt;
by eliminating the need for the subject-specific threshold. Our experimental results indicate that&lt;br /&gt;
the functional segmentation provides a robust, anatomically meaningful&lt;br /&gt;
and consistent model for functional connectivity in fMRI.&lt;br /&gt;
&lt;br /&gt;
We formulate the problem of characterizing connectivity as a partition of voxels into subsets that are well characterized by a certain number of representative hypotheses, or time courses, based on the similarity of their time courses to each hypothesis. We model the fMRI signal at each voxel as generated by a mixture of Gaussian distributions whose centers are the desired representative time courses. Using the EM algorithm to solve the corresponding model-fitting problem, we alternatively estimate the representative time courses and cluster assignments to improve our random initialization. &lt;br /&gt;
&lt;br /&gt;
''' ''Experimental Results'' '''&lt;br /&gt;
&lt;br /&gt;
We used data from 7 subjects with a diverse set of visual experiments including localizer, morphing, rest, internal tasks, and movie. The functional scans were pre-processed for motion artifacts, manually aligned into the Talairach coordinate system, detrended (removing linear trends in the&lt;br /&gt;
baseline activation) and smoothed (8mm kernel).&lt;br /&gt;
&lt;br /&gt;
Fig. 1 shows the 2-system partition extracted in each subject independently&lt;br /&gt;
of all others. It also displays the boundaries of the intrinsic system determined&lt;br /&gt;
through the traditional seed selection, showing good agreement between the two&lt;br /&gt;
partitions. Fig. 2 presents the results of further clustering the stimulus-driven cluster into two clusters independently for each subject. &lt;br /&gt;
&lt;br /&gt;
&amp;lt;table&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt; &amp;lt;th&amp;gt; '''Fig 1. 2-System Parcelation. Results for all 7 subjects.''' &amp;lt;th&amp;gt; '''Fig 2. 3-System Parcelation. Results for all 7 subjects.''' &lt;br /&gt;
&amp;lt;tr&amp;gt; &amp;lt;td align=&amp;quot;center&amp;quot;&amp;gt; &lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation2_shb1_4.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation2_shb5_6.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation2_shb7.png |400px]]&lt;br /&gt;
&amp;lt;td align=&amp;quot;center&amp;quot;&amp;gt;&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb1_3.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb4_5.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb6.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb7.png |400px]]&lt;br /&gt;
&amp;lt;/table&amp;gt;&lt;br /&gt;
&lt;br /&gt;
Fig.3 presents the group average of the subject-specific 2-system maps. Color shading shows the proportion of subjects whose clustering agreed with the majority label. Fig. 4 shows the group average of a further parcelation of the intrinsic system, i.e., one of two clusters associated with the non-stimulus-driven regions. In order to present a validation of the method, we compare these results with the conventional scheme for detection of visually responsive areas. In Fig. 5, color shows the statistical parametric map while solid lines indicate the boundaries of the visual system obtained through clustering. The result illustrate the agreement between the two methods.&lt;br /&gt;
&lt;br /&gt;
&amp;lt;table&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&amp;lt;th&amp;gt; '''Fig 3. 2-System Parcellation. Group-wise result.'''&lt;br /&gt;
&amp;lt;tr&amp;gt; &amp;lt;td align=&amp;quot;center&amp;quot;&amp;gt;&lt;br /&gt;
{|&lt;br /&gt;
|+ &lt;br /&gt;
|valign=&amp;quot;top&amp;quot;|[[Image:mit_fmri_clustering_parcellation2_xsub.png |thumb|700px]]&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/table&amp;gt;&lt;br /&gt;
&lt;br /&gt;
{|&lt;br /&gt;
|+ '''Fig 4. Validation: Parcelation of the intrinsic system.'''&lt;br /&gt;
|valign=&amp;quot;top&amp;quot;|[[Image:mit_fmri_clustering_intrinsicsystem.png |thumb|650px]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
{|&lt;br /&gt;
|+ '''Fig 5. Validation: Visual system.'''&lt;br /&gt;
|valign=&amp;quot;top&amp;quot;|[[Image:mit_fmri_clustering_validation.png |thumb|1150px]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''' ''Clustering Study of Domain Specificity in High Level Visual Cortex'' '''&lt;br /&gt;
&lt;br /&gt;
As a more specific application of clustering model-based algorithms, we are currently investigating devising clustering algorithms for detection of functional connectivity in high-level visual cortex. It is suggested that there are regions in the visual cortex with high selectivity to certain categories of visual stimuli. Currently, the conventional method for detection of these methods is based on statistical tests comparing response of each voxel in the brain to different visual categories to see if it shows considerably higher activation to one category. For example, the well-known FFA (Fusiform Face Area) is the set of voxels which show high activation to faces when compared to objects. We are working on using the clustering the visual cortex as a means to make this analysis automatic and further discover new structures in the high-level visual cortex.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''' ''Comparison of Data-Driven Analysis Methods for Identiﬁcation of Functional Connectivity in fMRI'' '''&lt;br /&gt;
&lt;br /&gt;
Although ICA and clustering rely on very diﬀerent assumptions on the underlying distributions, they produce surprisingly similar results for signals with large variation. Our main goal is to evaluate and compare the performance of ICA and a more general version of clustering, Gaussian mixture model (GMM) for identiﬁcation of functional connectivity. Using the synthetic data with artiﬁcial activations and artifacts under two experimental conditions (length of the time course and signal-to-noise ratio (SNR) of the data), both spatial maps and their associated time courses estimated by ICA and GMM are compared to each other and to the ground truth. The number of sources is chosen via the model selection scheme and all selected components are compared, not just the task-related components. This comparison scheme is veriﬁed in a real visual recognition fMRI study. We ﬁnd that ICA requires a smaller number of total components to extract the task-related components, but also needs a large number of total components to describe the entire data, whereas the diﬀerence between those values is small for GMM.&lt;br /&gt;
&lt;br /&gt;
= Key Investigators =&lt;br /&gt;
&lt;br /&gt;
* MIT Algorithms: Danial Lashkari, Y. Bryce Kim, Polina Golland, Nancy Kanwisher&lt;br /&gt;
&lt;br /&gt;
= Publications =&lt;br /&gt;
&lt;br /&gt;
''In print''&lt;br /&gt;
&lt;br /&gt;
* [http://www.na-mic.org/pages/Special:Publications?text=fMRI+Clustering&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;
''In press''&lt;br /&gt;
&lt;br /&gt;
* D. Lashkari, P. Golland. Convex Clustering with Exemplar-Based Models. In NIPS: Advances in Neural Information Processing Systems, 2007.&lt;br /&gt;
&lt;br /&gt;
[[Category:fMRI]]&lt;/div&gt;</summary>
		<author><name>Ybkim</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:fMRIClustering&amp;diff=24691</id>
		<title>Projects:fMRIClustering</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:fMRIClustering&amp;diff=24691"/>
		<updated>2008-05-16T20:18:13Z</updated>

		<summary type="html">&lt;p&gt;Ybkim: /* Description */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Back to [[NA-MIC_Internal_Collaborations:fMRIAnalysis|NA-MIC Collaborations]], [[Algorithm:MIT|MIT Algorithms]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
&lt;br /&gt;
= fMRI Clustering =&lt;br /&gt;
&lt;br /&gt;
One of the major goals in analysis of fMRI data is the detection of networks in the brain with similar functional behavior. A wide variety of methods  including hypothesis-driven statistical tests, unsupervised learning methods such as PCA and ICA, and different clustering algorithms have been employed to find these networks. This project aims to particularly study application of model-based clustering algorithms in identification of functional connectivity in the brain. &lt;br /&gt;
&lt;br /&gt;
= Description =&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
'''''Generative Model for Functional Connectivity'''''&lt;br /&gt;
&lt;br /&gt;
In the classical functional connectivity analysis, networks of interest are&lt;br /&gt;
defined based on correlation with the mean time course of a user-selected&lt;br /&gt;
`seed' region. Further, the user has to also specify a subject-specific threshold at which correlation&lt;br /&gt;
values are deemed significant. In this project, we simultaneously estimate the optimal&lt;br /&gt;
representative time courses that summarize the fMRI data well and&lt;br /&gt;
the partition of the volume into a set of disjoint regions that are best&lt;br /&gt;
explained by these representative time courses. This approach to functional connectivity analysis offers two&lt;br /&gt;
advantages. First, is removes the sensitivity of the analysis to the details&lt;br /&gt;
of the seed selection. Second, it substantially simplifies group analysis&lt;br /&gt;
by eliminating the need for the subject-specific threshold. Our experimental results indicate that&lt;br /&gt;
the functional segmentation provides a robust, anatomically meaningful&lt;br /&gt;
and consistent model for functional connectivity in fMRI.&lt;br /&gt;
&lt;br /&gt;
We formulate the problem of characterizing connectivity as a partition of voxels into subsets that are well characterized by a certain number of representative hypotheses, or time courses, based on the similarity of their time courses to each hypothesis. We model the fMRI signal at each voxel as generated by a mixture of Gaussian distributions whose centers are the desired representative time courses. Using the EM algorithm to solve the corresponding model-fitting problem, we alternatively estimate the representative time courses and cluster assignments to improve our random initialization. &lt;br /&gt;
&lt;br /&gt;
''' ''Experimental Results'' '''&lt;br /&gt;
&lt;br /&gt;
We used data from 7 subjects with a diverse set of visual experiments including localizer, morphing, rest, internal tasks, and movie. The functional scans were pre-processed for motion artifacts, manually aligned into the Talairach coordinate system, detrended (removing linear trends in the&lt;br /&gt;
baseline activation) and smoothed (8mm kernel).&lt;br /&gt;
&lt;br /&gt;
Fig. 1 shows the 2-system partition extracted in each subject independently&lt;br /&gt;
of all others. It also displays the boundaries of the intrinsic system determined&lt;br /&gt;
through the traditional seed selection, showing good agreement between the two&lt;br /&gt;
partitions. Fig. 2 presents the results of further clustering the stimulus-driven cluster into two clusters independently for each subject. &lt;br /&gt;
&lt;br /&gt;
&amp;lt;table&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt; &amp;lt;th&amp;gt; '''Fig 1. 2-System Parcelation. Results for all 7 subjects.''' &amp;lt;th&amp;gt; '''Fig 2. 3-System Parcelation. Results for all 7 subjects.''' &lt;br /&gt;
&amp;lt;tr&amp;gt; &amp;lt;td align=&amp;quot;center&amp;quot;&amp;gt; &lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation2_shb1_4.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation2_shb5_6.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation2_shb7.png |400px]]&lt;br /&gt;
&amp;lt;td align=&amp;quot;center&amp;quot;&amp;gt;&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb1_3.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb4_5.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb6.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb7.png |400px]]&lt;br /&gt;
&amp;lt;/table&amp;gt;&lt;br /&gt;
&lt;br /&gt;
Fig.3 presents the group average of the subject-specific 2-system maps. Color shading shows the proportion of subjects whose clustering agreed with the majority label. Fig. 4 shows the group average of a further parcelation of the intrinsic system, i.e., one of two clusters associated with the non-stimulus-driven regions. In order to present a validation of the method, we compare these results with the conventional scheme for detection of visually responsive areas. In Fig. 5, color shows the statistical parametric map while solid lines indicate the boundaries of the visual system obtained through clustering. The result illustrate the agreement between the two methods.&lt;br /&gt;
&lt;br /&gt;
&amp;lt;table&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&amp;lt;th&amp;gt; '''Fig 3. 2-System Parcellation. Group-wise result.'''&lt;br /&gt;
&amp;lt;tr&amp;gt; &amp;lt;td align=&amp;quot;center&amp;quot;&amp;gt;&lt;br /&gt;
{|&lt;br /&gt;
|+ &lt;br /&gt;
|valign=&amp;quot;top&amp;quot;|[[Image:mit_fmri_clustering_parcellation2_xsub.png |thumb|700px]]&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/table&amp;gt;&lt;br /&gt;
&lt;br /&gt;
{|&lt;br /&gt;
|+ '''Fig 4. Validation: Parcelation of the intrinsic system.'''&lt;br /&gt;
|valign=&amp;quot;top&amp;quot;|[[Image:mit_fmri_clustering_intrinsicsystem.png |thumb|650px]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
{|&lt;br /&gt;
|+ '''Fig 5. Validation: Visual system.'''&lt;br /&gt;
|valign=&amp;quot;top&amp;quot;|[[Image:mit_fmri_clustering_validation.png |thumb|1150px]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''' ''Clustering Study of Domain Specificity in High Level Visual Cortex'' '''&lt;br /&gt;
&lt;br /&gt;
As a more specific application of clustering model-based algorithms, we are currently investigating devising clustering algorithms for detection of functional connectivity in high-level visual cortex. It is suggested that there are regions in the visual cortex with high selectivity to certain categories of visual stimuli. Currently, the conventional method for detection of these methods is based on statistical tests comparing response of each voxel in the brain to different visual categories to see if it shows considerably higher activation to one category. For example, the well-known FFA (Fusiform Face Area) is the set of voxels which show high activation to faces when compared to objects. We are working on using the clustering the visual cortex as a means to make this analysis automatic and further discover new structures in the high-level visual cortex.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''' ''Comparison of Data-Driven Analysis Methods for Identiﬁcation of Functional Connectivity in fMRI'' '''&lt;br /&gt;
&lt;br /&gt;
= Key Investigators =&lt;br /&gt;
&lt;br /&gt;
* MIT Algorithms: Danial Lashkari, Y. Bryce Kim, Polina Golland, Nancy Kanwisher&lt;br /&gt;
&lt;br /&gt;
= Publications =&lt;br /&gt;
&lt;br /&gt;
''In print''&lt;br /&gt;
&lt;br /&gt;
* [http://www.na-mic.org/pages/Special:Publications?text=fMRI+Clustering&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;
''In press''&lt;br /&gt;
&lt;br /&gt;
* D. Lashkari, P. Golland. Convex Clustering with Exemplar-Based Models. In NIPS: Advances in Neural Information Processing Systems, 2007.&lt;br /&gt;
&lt;br /&gt;
[[Category:fMRI]]&lt;/div&gt;</summary>
		<author><name>Ybkim</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:fMRIClustering&amp;diff=24689</id>
		<title>Projects:fMRIClustering</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:fMRIClustering&amp;diff=24689"/>
		<updated>2008-05-16T20:16:43Z</updated>

		<summary type="html">&lt;p&gt;Ybkim: /* Description */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Back to [[NA-MIC_Internal_Collaborations:fMRIAnalysis|NA-MIC Collaborations]], [[Algorithm:MIT|MIT Algorithms]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
&lt;br /&gt;
= fMRI Clustering =&lt;br /&gt;
&lt;br /&gt;
One of the major goals in analysis of fMRI data is the detection of networks in the brain with similar functional behavior. A wide variety of methods  including hypothesis-driven statistical tests, unsupervised learning methods such as PCA and ICA, and different clustering algorithms have been employed to find these networks. This project aims to particularly study application of model-based clustering algorithms in identification of functional connectivity in the brain. &lt;br /&gt;
&lt;br /&gt;
= Description =&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
'''''Generative Model for Functional Connectivity'''''&lt;br /&gt;
&lt;br /&gt;
In the classical functional connectivity analysis, networks of interest are&lt;br /&gt;
defined based on correlation with the mean time course of a user-selected&lt;br /&gt;
`seed' region. Further, the user has to also specify a subject-specific threshold at which correlation&lt;br /&gt;
values are deemed significant. In this project, we simultaneously estimate the optimal&lt;br /&gt;
representative time courses that summarize the fMRI data well and&lt;br /&gt;
the partition of the volume into a set of disjoint regions that are best&lt;br /&gt;
explained by these representative time courses. This approach to functional connectivity analysis offers two&lt;br /&gt;
advantages. First, is removes the sensitivity of the analysis to the details&lt;br /&gt;
of the seed selection. Second, it substantially simplifies group analysis&lt;br /&gt;
by eliminating the need for the subject-specific threshold. Our experimental results indicate that&lt;br /&gt;
the functional segmentation provides a robust, anatomically meaningful&lt;br /&gt;
and consistent model for functional connectivity in fMRI.&lt;br /&gt;
&lt;br /&gt;
We formulate the problem of characterizing connectivity as a partition of voxels into subsets that are well characterized by a certain number of representative hypotheses, or time courses, based on the similarity of their time courses to each hypothesis. We model the fMRI signal at each voxel as generated by a mixture of Gaussian distributions whose centers are the desired representative time courses. Using the EM algorithm to solve the corresponding model-fitting problem, we alternatively estimate the representative time courses and cluster assignments to improve our random initialization. &lt;br /&gt;
&lt;br /&gt;
''' ''Experimental Results'' '''&lt;br /&gt;
&lt;br /&gt;
We used data from 7 subjects with a diverse set of visual experiments including localizer, morphing, rest, internal tasks, and movie. The functional scans were pre-processed for motion artifacts, manually aligned into the Talairach coordinate system, detrended (removing linear trends in the&lt;br /&gt;
baseline activation) and smoothed (8mm kernel).&lt;br /&gt;
&lt;br /&gt;
Fig. 1 shows the 2-system partition extracted in each subject independently&lt;br /&gt;
of all others. It also displays the boundaries of the intrinsic system determined&lt;br /&gt;
through the traditional seed selection, showing good agreement between the two&lt;br /&gt;
partitions. Fig. 2 presents the results of further clustering the stimulus-driven cluster into two clusters independently for each subject. &lt;br /&gt;
&lt;br /&gt;
&amp;lt;table&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt; &amp;lt;th&amp;gt; '''Fig 1. 2-System Parcelation. Results for all 7 subjects.''' &amp;lt;th&amp;gt; '''Fig 2. 3-System Parcelation. Results for all 7 subjects.''' &lt;br /&gt;
&amp;lt;tr&amp;gt; &amp;lt;td align=&amp;quot;center&amp;quot;&amp;gt; &lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation2_shb1_4.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation2_shb5_6.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation2_shb7.png |400px]]&lt;br /&gt;
&amp;lt;td align=&amp;quot;center&amp;quot;&amp;gt;&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb1_3.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb4_5.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb6.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb7.png |400px]]&lt;br /&gt;
&amp;lt;/table&amp;gt;&lt;br /&gt;
&lt;br /&gt;
Fig.3 presents the group average of the subject-specific 2-system maps. Color shading shows the proportion of subjects whose clustering agreed with the majority label. Fig. 4 shows the group average of a further parcelation of the intrinsic system, i.e., one of two clusters associated with the non-stimulus-driven regions. In order to present a validation of the method, we compare these results with the conventional scheme for detection of visually responsive areas. In Fig. 5, color shows the statistical parametric map while solid lines indicate the boundaries of the visual system obtained through clustering. The result illustrate the agreement between the two methods.&lt;br /&gt;
&lt;br /&gt;
&amp;lt;table&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&amp;lt;th&amp;gt; '''Fig 3. 2-System Parcellation. Group-wise result.'''&lt;br /&gt;
&amp;lt;tr&amp;gt; &amp;lt;td align=&amp;quot;center&amp;quot;&amp;gt;&lt;br /&gt;
{|&lt;br /&gt;
|+ &lt;br /&gt;
|valign=&amp;quot;top&amp;quot;|[[Image:mit_fmri_clustering_parcellation2_xsub.png |thumb|700px]]&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/table&amp;gt;&lt;br /&gt;
&lt;br /&gt;
{|&lt;br /&gt;
|+ '''Fig 4. Validation: Parcelation of the intrinsic system.'''&lt;br /&gt;
|valign=&amp;quot;top&amp;quot;|[[Image:mit_fmri_clustering_intrinsicsystem.png |thumb|650px]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
{|&lt;br /&gt;
|+ '''Fig 5. Validation: Visual system.'''&lt;br /&gt;
|valign=&amp;quot;top&amp;quot;|[[Image:mit_fmri_clustering_validation.png |thumb|1150px]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''' ''Clustering Study of Domain Specificity in High Level Visual Cortex'' '''&lt;br /&gt;
&lt;br /&gt;
As a more specific application of clustering model-based algorithms, we are currently investigating devising clustering algorithms for detection of functional connectivity in high-level visual cortex. It is suggested that there are regions in the visual cortex with high selectivity to certain categories of visual stimuli. Currently, the conventional method for detection of these methods is based on statistical tests comparing response of each voxel in the brain to different visual categories to see if it shows considerably higher activation to one category. For example, the well-known FFA (Fusiform Face Area) is the set of voxels which show high activation to faces when compared to objects. We are working on using the clustering the visual cortex as a means to make this analysis automatic and further discover new structures in the high-level visual cortex.&lt;br /&gt;
&lt;br /&gt;
''' ''Clustering Study of Domain Specificity in High Level Visual Cortex'' '''&lt;br /&gt;
&lt;br /&gt;
= Key Investigators =&lt;br /&gt;
&lt;br /&gt;
* MIT Algorithms: Danial Lashkari, Y. Bryce Kim, Polina Golland, Nancy Kanwisher&lt;br /&gt;
&lt;br /&gt;
= Publications =&lt;br /&gt;
&lt;br /&gt;
''In print''&lt;br /&gt;
&lt;br /&gt;
* [http://www.na-mic.org/pages/Special:Publications?text=fMRI+Clustering&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;
''In press''&lt;br /&gt;
&lt;br /&gt;
* D. Lashkari, P. Golland. Convex Clustering with Exemplar-Based Models. In NIPS: Advances in Neural Information Processing Systems, 2007.&lt;br /&gt;
&lt;br /&gt;
[[Category:fMRI]]&lt;/div&gt;</summary>
		<author><name>Ybkim</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:fMRIClustering&amp;diff=24687</id>
		<title>Projects:fMRIClustering</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:fMRIClustering&amp;diff=24687"/>
		<updated>2008-05-16T20:15:30Z</updated>

		<summary type="html">&lt;p&gt;Ybkim: /* Key Investigators */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Back to [[NA-MIC_Internal_Collaborations:fMRIAnalysis|NA-MIC Collaborations]], [[Algorithm:MIT|MIT Algorithms]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
&lt;br /&gt;
= fMRI Clustering =&lt;br /&gt;
&lt;br /&gt;
One of the major goals in analysis of fMRI data is the detection of networks in the brain with similar functional behavior. A wide variety of methods  including hypothesis-driven statistical tests, unsupervised learning methods such as PCA and ICA, and different clustering algorithms have been employed to find these networks. This project aims to particularly study application of model-based clustering algorithms in identification of functional connectivity in the brain. &lt;br /&gt;
&lt;br /&gt;
= Description =&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
'''''Generative Model for Functional Connectivity'''''&lt;br /&gt;
&lt;br /&gt;
In the classical functional connectivity analysis, networks of interest are&lt;br /&gt;
defined based on correlation with the mean time course of a user-selected&lt;br /&gt;
`seed' region. Further, the user has to also specify a subject-specific threshold at which correlation&lt;br /&gt;
values are deemed significant. In this project, we simultaneously estimate the optimal&lt;br /&gt;
representative time courses that summarize the fMRI data well and&lt;br /&gt;
the partition of the volume into a set of disjoint regions that are best&lt;br /&gt;
explained by these representative time courses. This approach to functional connectivity analysis offers two&lt;br /&gt;
advantages. First, is removes the sensitivity of the analysis to the details&lt;br /&gt;
of the seed selection. Second, it substantially simplifies group analysis&lt;br /&gt;
by eliminating the need for the subject-specific threshold. Our experimental results indicate that&lt;br /&gt;
the functional segmentation provides a robust, anatomically meaningful&lt;br /&gt;
and consistent model for functional connectivity in fMRI.&lt;br /&gt;
&lt;br /&gt;
We formulate the problem of characterizing connectivity as a partition of voxels into subsets that are well characterized by a certain number of representative hypotheses, or time courses, based on the similarity of their time courses to each hypothesis. We model the fMRI signal at each voxel as generated by a mixture of Gaussian distributions whose centers are the desired representative time courses. Using the EM algorithm to solve the corresponding model-fitting problem, we alternatively estimate the representative time courses and cluster assignments to improve our random initialization. &lt;br /&gt;
&lt;br /&gt;
''' ''Experimental Results'' '''&lt;br /&gt;
&lt;br /&gt;
We used data from 7 subjects with a diverse set of visual experiments including localizer, morphing, rest, internal tasks, and movie. The functional scans were pre-processed for motion artifacts, manually aligned into the Talairach coordinate system, detrended (removing linear trends in the&lt;br /&gt;
baseline activation) and smoothed (8mm kernel).&lt;br /&gt;
&lt;br /&gt;
Fig. 1 shows the 2-system partition extracted in each subject independently&lt;br /&gt;
of all others. It also displays the boundaries of the intrinsic system determined&lt;br /&gt;
through the traditional seed selection, showing good agreement between the two&lt;br /&gt;
partitions. Fig. 2 presents the results of further clustering the stimulus-driven cluster into two clusters independently for each subject. &lt;br /&gt;
&lt;br /&gt;
&amp;lt;table&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt; &amp;lt;th&amp;gt; '''Fig 1. 2-System Parcelation. Results for all 7 subjects.''' &amp;lt;th&amp;gt; '''Fig 2. 3-System Parcelation. Results for all 7 subjects.''' &lt;br /&gt;
&amp;lt;tr&amp;gt; &amp;lt;td align=&amp;quot;center&amp;quot;&amp;gt; &lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation2_shb1_4.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation2_shb5_6.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation2_shb7.png |400px]]&lt;br /&gt;
&amp;lt;td align=&amp;quot;center&amp;quot;&amp;gt;&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb1_3.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb4_5.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb6.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb7.png |400px]]&lt;br /&gt;
&amp;lt;/table&amp;gt;&lt;br /&gt;
&lt;br /&gt;
Fig.3 presents the group average of the subject-specific 2-system maps. Color shading shows the proportion of subjects whose clustering agreed with the majority label. Fig. 4 shows the group average of a further parcelation of the intrinsic system, i.e., one of two clusters associated with the non-stimulus-driven regions. In order to present a validation of the method, we compare these results with the conventional scheme for detection of visually responsive areas. In Fig. 5, color shows the statistical parametric map while solid lines indicate the boundaries of the visual system obtained through clustering. The result illustrate the agreement between the two methods.&lt;br /&gt;
&lt;br /&gt;
&amp;lt;table&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&amp;lt;th&amp;gt; '''Fig 3. 2-System Parcellation. Group-wise result.'''&lt;br /&gt;
&amp;lt;tr&amp;gt; &amp;lt;td align=&amp;quot;center&amp;quot;&amp;gt;&lt;br /&gt;
{|&lt;br /&gt;
|+ &lt;br /&gt;
|valign=&amp;quot;top&amp;quot;|[[Image:mit_fmri_clustering_parcellation2_xsub.png |thumb|700px]]&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/table&amp;gt;&lt;br /&gt;
&lt;br /&gt;
{|&lt;br /&gt;
|+ '''Fig 4. Validation: Parcelation of the intrinsic system.'''&lt;br /&gt;
|valign=&amp;quot;top&amp;quot;|[[Image:mit_fmri_clustering_intrinsicsystem.png |thumb|650px]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
{|&lt;br /&gt;
|+ '''Fig 5. Validation: Visual system.'''&lt;br /&gt;
|valign=&amp;quot;top&amp;quot;|[[Image:mit_fmri_clustering_validation.png |thumb|1150px]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''' ''Clustering Study of Domain Specificity in High Level Visual Cortex'' '''&lt;br /&gt;
&lt;br /&gt;
As a more specific application of clustering model-based algorithms, we are currently investigating devising clustering algorithms for detection of functional connectivity in high-level visual cortex. It is suggested that there are regions in the visual cortex with high selectivity to certain categories of visual stimuli. Currently, the conventional method for detection of these methods is based on statistical tests comparing response of each voxel in the brain to different visual categories to see if it shows considerably higher activation to one category. For example, the well-known FFA (Fusiform Face Area) is the set of voxels which show high activation to faces when compared to objects. We are working on using the clustering the visual cortex as a means to make this analysis automatic and further discover new structures in the high-level visual cortex.&lt;br /&gt;
&lt;br /&gt;
&amp;quot;Bryce&amp;quot;&lt;br /&gt;
&lt;br /&gt;
= Key Investigators =&lt;br /&gt;
&lt;br /&gt;
* MIT Algorithms: Danial Lashkari, Y. Bryce Kim, Polina Golland, Nancy Kanwisher&lt;br /&gt;
&lt;br /&gt;
= Publications =&lt;br /&gt;
&lt;br /&gt;
''In print''&lt;br /&gt;
&lt;br /&gt;
* [http://www.na-mic.org/pages/Special:Publications?text=fMRI+Clustering&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;
''In press''&lt;br /&gt;
&lt;br /&gt;
* D. Lashkari, P. Golland. Convex Clustering with Exemplar-Based Models. In NIPS: Advances in Neural Information Processing Systems, 2007.&lt;br /&gt;
&lt;br /&gt;
[[Category:fMRI]]&lt;/div&gt;</summary>
		<author><name>Ybkim</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:fMRIClustering&amp;diff=24686</id>
		<title>Projects:fMRIClustering</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:fMRIClustering&amp;diff=24686"/>
		<updated>2008-05-16T20:15:17Z</updated>

		<summary type="html">&lt;p&gt;Ybkim: /* Key Investigators */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Back to [[NA-MIC_Internal_Collaborations:fMRIAnalysis|NA-MIC Collaborations]], [[Algorithm:MIT|MIT Algorithms]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
&lt;br /&gt;
= fMRI Clustering =&lt;br /&gt;
&lt;br /&gt;
One of the major goals in analysis of fMRI data is the detection of networks in the brain with similar functional behavior. A wide variety of methods  including hypothesis-driven statistical tests, unsupervised learning methods such as PCA and ICA, and different clustering algorithms have been employed to find these networks. This project aims to particularly study application of model-based clustering algorithms in identification of functional connectivity in the brain. &lt;br /&gt;
&lt;br /&gt;
= Description =&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
'''''Generative Model for Functional Connectivity'''''&lt;br /&gt;
&lt;br /&gt;
In the classical functional connectivity analysis, networks of interest are&lt;br /&gt;
defined based on correlation with the mean time course of a user-selected&lt;br /&gt;
`seed' region. Further, the user has to also specify a subject-specific threshold at which correlation&lt;br /&gt;
values are deemed significant. In this project, we simultaneously estimate the optimal&lt;br /&gt;
representative time courses that summarize the fMRI data well and&lt;br /&gt;
the partition of the volume into a set of disjoint regions that are best&lt;br /&gt;
explained by these representative time courses. This approach to functional connectivity analysis offers two&lt;br /&gt;
advantages. First, is removes the sensitivity of the analysis to the details&lt;br /&gt;
of the seed selection. Second, it substantially simplifies group analysis&lt;br /&gt;
by eliminating the need for the subject-specific threshold. Our experimental results indicate that&lt;br /&gt;
the functional segmentation provides a robust, anatomically meaningful&lt;br /&gt;
and consistent model for functional connectivity in fMRI.&lt;br /&gt;
&lt;br /&gt;
We formulate the problem of characterizing connectivity as a partition of voxels into subsets that are well characterized by a certain number of representative hypotheses, or time courses, based on the similarity of their time courses to each hypothesis. We model the fMRI signal at each voxel as generated by a mixture of Gaussian distributions whose centers are the desired representative time courses. Using the EM algorithm to solve the corresponding model-fitting problem, we alternatively estimate the representative time courses and cluster assignments to improve our random initialization. &lt;br /&gt;
&lt;br /&gt;
''' ''Experimental Results'' '''&lt;br /&gt;
&lt;br /&gt;
We used data from 7 subjects with a diverse set of visual experiments including localizer, morphing, rest, internal tasks, and movie. The functional scans were pre-processed for motion artifacts, manually aligned into the Talairach coordinate system, detrended (removing linear trends in the&lt;br /&gt;
baseline activation) and smoothed (8mm kernel).&lt;br /&gt;
&lt;br /&gt;
Fig. 1 shows the 2-system partition extracted in each subject independently&lt;br /&gt;
of all others. It also displays the boundaries of the intrinsic system determined&lt;br /&gt;
through the traditional seed selection, showing good agreement between the two&lt;br /&gt;
partitions. Fig. 2 presents the results of further clustering the stimulus-driven cluster into two clusters independently for each subject. &lt;br /&gt;
&lt;br /&gt;
&amp;lt;table&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt; &amp;lt;th&amp;gt; '''Fig 1. 2-System Parcelation. Results for all 7 subjects.''' &amp;lt;th&amp;gt; '''Fig 2. 3-System Parcelation. Results for all 7 subjects.''' &lt;br /&gt;
&amp;lt;tr&amp;gt; &amp;lt;td align=&amp;quot;center&amp;quot;&amp;gt; &lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation2_shb1_4.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation2_shb5_6.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation2_shb7.png |400px]]&lt;br /&gt;
&amp;lt;td align=&amp;quot;center&amp;quot;&amp;gt;&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb1_3.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb4_5.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb6.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb7.png |400px]]&lt;br /&gt;
&amp;lt;/table&amp;gt;&lt;br /&gt;
&lt;br /&gt;
Fig.3 presents the group average of the subject-specific 2-system maps. Color shading shows the proportion of subjects whose clustering agreed with the majority label. Fig. 4 shows the group average of a further parcelation of the intrinsic system, i.e., one of two clusters associated with the non-stimulus-driven regions. In order to present a validation of the method, we compare these results with the conventional scheme for detection of visually responsive areas. In Fig. 5, color shows the statistical parametric map while solid lines indicate the boundaries of the visual system obtained through clustering. The result illustrate the agreement between the two methods.&lt;br /&gt;
&lt;br /&gt;
&amp;lt;table&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&amp;lt;th&amp;gt; '''Fig 3. 2-System Parcellation. Group-wise result.'''&lt;br /&gt;
&amp;lt;tr&amp;gt; &amp;lt;td align=&amp;quot;center&amp;quot;&amp;gt;&lt;br /&gt;
{|&lt;br /&gt;
|+ &lt;br /&gt;
|valign=&amp;quot;top&amp;quot;|[[Image:mit_fmri_clustering_parcellation2_xsub.png |thumb|700px]]&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/table&amp;gt;&lt;br /&gt;
&lt;br /&gt;
{|&lt;br /&gt;
|+ '''Fig 4. Validation: Parcelation of the intrinsic system.'''&lt;br /&gt;
|valign=&amp;quot;top&amp;quot;|[[Image:mit_fmri_clustering_intrinsicsystem.png |thumb|650px]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
{|&lt;br /&gt;
|+ '''Fig 5. Validation: Visual system.'''&lt;br /&gt;
|valign=&amp;quot;top&amp;quot;|[[Image:mit_fmri_clustering_validation.png |thumb|1150px]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''' ''Clustering Study of Domain Specificity in High Level Visual Cortex'' '''&lt;br /&gt;
&lt;br /&gt;
As a more specific application of clustering model-based algorithms, we are currently investigating devising clustering algorithms for detection of functional connectivity in high-level visual cortex. It is suggested that there are regions in the visual cortex with high selectivity to certain categories of visual stimuli. Currently, the conventional method for detection of these methods is based on statistical tests comparing response of each voxel in the brain to different visual categories to see if it shows considerably higher activation to one category. For example, the well-known FFA (Fusiform Face Area) is the set of voxels which show high activation to faces when compared to objects. We are working on using the clustering the visual cortex as a means to make this analysis automatic and further discover new structures in the high-level visual cortex.&lt;br /&gt;
&lt;br /&gt;
&amp;quot;Bryce&amp;quot;&lt;br /&gt;
&lt;br /&gt;
= Key Investigators =&lt;br /&gt;
&lt;br /&gt;
* MIT Algorithms: Danial Lashkari, W. Bryce Kim, Polina Golland, Nancy Kanwisher&lt;br /&gt;
&lt;br /&gt;
= Publications =&lt;br /&gt;
&lt;br /&gt;
''In print''&lt;br /&gt;
&lt;br /&gt;
* [http://www.na-mic.org/pages/Special:Publications?text=fMRI+Clustering&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;
''In press''&lt;br /&gt;
&lt;br /&gt;
* D. Lashkari, P. Golland. Convex Clustering with Exemplar-Based Models. In NIPS: Advances in Neural Information Processing Systems, 2007.&lt;br /&gt;
&lt;br /&gt;
[[Category:fMRI]]&lt;/div&gt;</summary>
		<author><name>Ybkim</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=Projects:fMRIClustering&amp;diff=24677</id>
		<title>Projects:fMRIClustering</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=Projects:fMRIClustering&amp;diff=24677"/>
		<updated>2008-05-16T20:05:49Z</updated>

		<summary type="html">&lt;p&gt;Ybkim: /* Description */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Back to [[NA-MIC_Internal_Collaborations:fMRIAnalysis|NA-MIC Collaborations]], [[Algorithm:MIT|MIT Algorithms]]&lt;br /&gt;
__NOTOC__&lt;br /&gt;
&lt;br /&gt;
= fMRI Clustering =&lt;br /&gt;
&lt;br /&gt;
One of the major goals in analysis of fMRI data is the detection of networks in the brain with similar functional behavior. A wide variety of methods  including hypothesis-driven statistical tests, unsupervised learning methods such as PCA and ICA, and different clustering algorithms have been employed to find these networks. This project aims to particularly study application of model-based clustering algorithms in identification of functional connectivity in the brain. &lt;br /&gt;
&lt;br /&gt;
= Description =&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
'''''Generative Model for Functional Connectivity'''''&lt;br /&gt;
&lt;br /&gt;
In the classical functional connectivity analysis, networks of interest are&lt;br /&gt;
defined based on correlation with the mean time course of a user-selected&lt;br /&gt;
`seed' region. Further, the user has to also specify a subject-specific threshold at which correlation&lt;br /&gt;
values are deemed significant. In this project, we simultaneously estimate the optimal&lt;br /&gt;
representative time courses that summarize the fMRI data well and&lt;br /&gt;
the partition of the volume into a set of disjoint regions that are best&lt;br /&gt;
explained by these representative time courses. This approach to functional connectivity analysis offers two&lt;br /&gt;
advantages. First, is removes the sensitivity of the analysis to the details&lt;br /&gt;
of the seed selection. Second, it substantially simplifies group analysis&lt;br /&gt;
by eliminating the need for the subject-specific threshold. Our experimental results indicate that&lt;br /&gt;
the functional segmentation provides a robust, anatomically meaningful&lt;br /&gt;
and consistent model for functional connectivity in fMRI.&lt;br /&gt;
&lt;br /&gt;
We formulate the problem of characterizing connectivity as a partition of voxels into subsets that are well characterized by a certain number of representative hypotheses, or time courses, based on the similarity of their time courses to each hypothesis. We model the fMRI signal at each voxel as generated by a mixture of Gaussian distributions whose centers are the desired representative time courses. Using the EM algorithm to solve the corresponding model-fitting problem, we alternatively estimate the representative time courses and cluster assignments to improve our random initialization. &lt;br /&gt;
&lt;br /&gt;
''' ''Experimental Results'' '''&lt;br /&gt;
&lt;br /&gt;
We used data from 7 subjects with a diverse set of visual experiments including localizer, morphing, rest, internal tasks, and movie. The functional scans were pre-processed for motion artifacts, manually aligned into the Talairach coordinate system, detrended (removing linear trends in the&lt;br /&gt;
baseline activation) and smoothed (8mm kernel).&lt;br /&gt;
&lt;br /&gt;
Fig. 1 shows the 2-system partition extracted in each subject independently&lt;br /&gt;
of all others. It also displays the boundaries of the intrinsic system determined&lt;br /&gt;
through the traditional seed selection, showing good agreement between the two&lt;br /&gt;
partitions. Fig. 2 presents the results of further clustering the stimulus-driven cluster into two clusters independently for each subject. &lt;br /&gt;
&lt;br /&gt;
&amp;lt;table&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt; &amp;lt;th&amp;gt; '''Fig 1. 2-System Parcelation. Results for all 7 subjects.''' &amp;lt;th&amp;gt; '''Fig 2. 3-System Parcelation. Results for all 7 subjects.''' &lt;br /&gt;
&amp;lt;tr&amp;gt; &amp;lt;td align=&amp;quot;center&amp;quot;&amp;gt; &lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation2_shb1_4.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation2_shb5_6.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation2_shb7.png |400px]]&lt;br /&gt;
&amp;lt;td align=&amp;quot;center&amp;quot;&amp;gt;&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb1_3.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb4_5.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb6.png |400px]]&lt;br /&gt;
[[Image:mit_fmri_clustering_parcellation3_shb7.png |400px]]&lt;br /&gt;
&amp;lt;/table&amp;gt;&lt;br /&gt;
&lt;br /&gt;
Fig.3 presents the group average of the subject-specific 2-system maps. Color shading shows the proportion of subjects whose clustering agreed with the majority label. Fig. 4 shows the group average of a further parcelation of the intrinsic system, i.e., one of two clusters associated with the non-stimulus-driven regions. In order to present a validation of the method, we compare these results with the conventional scheme for detection of visually responsive areas. In Fig. 5, color shows the statistical parametric map while solid lines indicate the boundaries of the visual system obtained through clustering. The result illustrate the agreement between the two methods.&lt;br /&gt;
&lt;br /&gt;
&amp;lt;table&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&amp;lt;th&amp;gt; '''Fig 3. 2-System Parcellation. Group-wise result.'''&lt;br /&gt;
&amp;lt;tr&amp;gt; &amp;lt;td align=&amp;quot;center&amp;quot;&amp;gt;&lt;br /&gt;
{|&lt;br /&gt;
|+ &lt;br /&gt;
|valign=&amp;quot;top&amp;quot;|[[Image:mit_fmri_clustering_parcellation2_xsub.png |thumb|700px]]&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/table&amp;gt;&lt;br /&gt;
&lt;br /&gt;
{|&lt;br /&gt;
|+ '''Fig 4. Validation: Parcelation of the intrinsic system.'''&lt;br /&gt;
|valign=&amp;quot;top&amp;quot;|[[Image:mit_fmri_clustering_intrinsicsystem.png |thumb|650px]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
{|&lt;br /&gt;
|+ '''Fig 5. Validation: Visual system.'''&lt;br /&gt;
|valign=&amp;quot;top&amp;quot;|[[Image:mit_fmri_clustering_validation.png |thumb|1150px]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
''' ''Clustering Study of Domain Specificity in High Level Visual Cortex'' '''&lt;br /&gt;
&lt;br /&gt;
As a more specific application of clustering model-based algorithms, we are currently investigating devising clustering algorithms for detection of functional connectivity in high-level visual cortex. It is suggested that there are regions in the visual cortex with high selectivity to certain categories of visual stimuli. Currently, the conventional method for detection of these methods is based on statistical tests comparing response of each voxel in the brain to different visual categories to see if it shows considerably higher activation to one category. For example, the well-known FFA (Fusiform Face Area) is the set of voxels which show high activation to faces when compared to objects. We are working on using the clustering the visual cortex as a means to make this analysis automatic and further discover new structures in the high-level visual cortex.&lt;br /&gt;
&lt;br /&gt;
&amp;quot;Bryce&amp;quot;&lt;br /&gt;
&lt;br /&gt;
= Key Investigators =&lt;br /&gt;
&lt;br /&gt;
* MIT Algorithms: Danial Lashkari, Polina Golland, Nancy Kanwisher &lt;br /&gt;
&lt;br /&gt;
= Publications =&lt;br /&gt;
&lt;br /&gt;
''In print''&lt;br /&gt;
&lt;br /&gt;
* [http://www.na-mic.org/pages/Special:Publications?text=fMRI+Clustering&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;
''In press''&lt;br /&gt;
&lt;br /&gt;
* D. Lashkari, P. Golland. Convex Clustering with Exemplar-Based Models. In NIPS: Advances in Neural Information Processing Systems, 2007.&lt;br /&gt;
&lt;br /&gt;
[[Category:fMRI]]&lt;/div&gt;</summary>
		<author><name>Ybkim</name></author>
		
	</entry>
	<entry>
		<id>https://www.na-mic.org/w/index.php?title=2008_Summer_Project_Week&amp;diff=24643</id>
		<title>2008 Summer Project Week</title>
		<link rel="alternate" type="text/html" href="https://www.na-mic.org/w/index.php?title=2008_Summer_Project_Week&amp;diff=24643"/>
		<updated>2008-05-15T19:49:00Z</updated>

		<summary type="html">&lt;p&gt;Ybkim: /* Attendee List */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Back to [[Engineering:Programming_Events|Programming/Project Events]]&lt;br /&gt;
&lt;br /&gt;
[[Image:ProjectWeek-2008.png|thumb|220px|right|Summer 2008]]&lt;br /&gt;
&lt;br /&gt;
== Logistics ==&lt;br /&gt;
&lt;br /&gt;
'''Dates:''' June 23-27, 2008&lt;br /&gt;
&lt;br /&gt;
'''Location:''' MIT. [[Meeting_Locations:MIT_Grier_A_%26B|Grier Rooms A &amp;amp; B: 34-401A &amp;amp; 34-401B]].&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
'''Registration Fee:''' $260 (this will cover the cost of breakfast, lunch and coffee breaks for the week). Due by Friday, June 13th, 2008. Please make checks out to &amp;quot;Massachusetts Institute of Technology&amp;quot; and mail to: Donna Kaufman, MIT, 77 Massachusetts Ave., 38-409a, Cambridge, MA 02139&lt;br /&gt;
&lt;br /&gt;
If you are attending for one day only, the registration fee is not required.&lt;br /&gt;
&lt;br /&gt;
'''Hotel:''' We have a group rate of $239/night (plus tax) at the [http://www.hotelatmit.com Hotel at MIT (now called Le Meridien)]. (Use group code NAM.) Here is some information about several other Boston area hotels that are convenient to NA-MIC events: [[Boston_Hotels|Boston_Hotels]]. Summer is tourist season in Boston, so please book your rooms early.&lt;br /&gt;
&lt;br /&gt;
([[Project Week Logistics Checklist|This is a checklist for the onsite planning items]])&lt;br /&gt;
&lt;br /&gt;
==Introduction to NA-MIC Project Week==&lt;br /&gt;
&lt;br /&gt;
NA-MIC Project Week is a hands on activity -- programming using the [[NA-MIC-Kit|NA-MIC Kit]], algorithm design, and clinical application -- that has become one of the major events in the [[NA-MIC-Kit|NA-MIC Kit]] calendar. This event is the seventh of the [[Engineering:Programming_Events|'''series''']]. It is held in the summer at MIT (typically the last week of June), and a shorter version is held in Salt Lake City in the winter (typically the second week of January).  &lt;br /&gt;
The main goal of these events if to move forward the deliverables of NA-MIC. NA-MIC participants and their collaborators are welcome to attend.  &lt;br /&gt;
&lt;br /&gt;
* NA-MIC Members: Participation in this event is voluntary -- if you don't think this will help you move forward in your work, there is no obligation to attend.&lt;br /&gt;
* Ideal candidates are those who want to contribute to the [[NA-MIC-Kit|NA-MIC Kit]], and those who can help make it happen.&lt;br /&gt;
* This is not an introduction to the components of the [[NA-MIC-Kit|NA-MIC Kit]].&lt;br /&gt;
* NA-MIC Core 1 (Algorithms) - bring your algorithms and code to work on in the company of Core 2 engineers and Core 3 scientists.&lt;br /&gt;
* NA-MIC Core 2 (Engineering) - bring your code for infrastructure and applications to extend the [[NA-MIC-Kit|NA-MIC Kit]] capabilities, integrate Core 1 algorithms, and refine workflows for Core 3.&lt;br /&gt;
* NA-MIC Core 3 (DBP) - bring your data to work on with the [[NA-MIC-Kit|NA-MIC Kit]] and get assistance and provide feedback to Core 1 scientists and Core 2 engineers.&lt;br /&gt;
* External Collaborators - if you are working on a project that uses the [[NA-MIC-Kit|NA-MIC kit]], and want to participate to get help from NA-MIC Engineering, please send an email to Tina Kapur (tkapur at bwh.harvard.edu).  Please note that the event is open to people outside NA-MIC, subject to availability.&lt;br /&gt;
* Everyone should '''bring a laptop'''. We will have four projectors.&lt;br /&gt;
* About half the time will be spent working on projects and the other half in project related discussions.&lt;br /&gt;
* You '''do''' need to be actively working on a NA-MIC related project in order to make this investment worthwhile for everyone.&lt;br /&gt;
&lt;br /&gt;
== Agenda==&lt;br /&gt;
* Monday &lt;br /&gt;
** noon-1pm lunch &lt;br /&gt;
**1pm: Welcome (Ron Kikinis)&lt;br /&gt;
** 1:05-3:30pm Introduce [[#Projects|Projects]] using templated wiki pages (all Project Leads) ([[NA-MIC/Projects/Theme/Template|Wiki Template]]) &lt;br /&gt;
** 3:30-5:30pm Start project work&lt;br /&gt;
* Tuesday &lt;br /&gt;
** 8:30am breakfast&lt;br /&gt;
** 9:00-9:45am: NA-MIC Software Process &lt;br /&gt;
** 10-10:30am [[Project Week 2008 Slicer 3.0 Update|Slicer 3.0 Update]] (Jim Miller, Steve Pieper)&lt;br /&gt;
** noon lunch&lt;br /&gt;
** 2:30-3:30pm: [[Project Week 2008 Special topic breakout: Non-Linear Registration]] &lt;br /&gt;
** 5:30pm adjourn for day&lt;br /&gt;
* Wednesday &lt;br /&gt;
** 8:30am breakfast&lt;br /&gt;
** 9:00-12pm [[Project Week 2008 Special topic breakout: ITK]] (Luis Ibanez)&lt;br /&gt;
** noon lunch&lt;br /&gt;
** 2:30-3:30pm: [[Project Week 2008 Special topic breakout: XNAT Database]] (Daniel Marcus)&lt;br /&gt;
** 5:30pm adjourn for day&lt;br /&gt;
* Thursday&lt;br /&gt;
** 8:30am breakfast&lt;br /&gt;
** noon lunch&lt;br /&gt;
**2:30-3:30pm [[Project Week 2008 Special topic breakout: GWE]] (Marco Ruiz)&lt;br /&gt;
** 5:30pm adjourn for day&lt;br /&gt;
* Friday &lt;br /&gt;
** 8:30am breakfast&lt;br /&gt;
** 10am-noon: Project Progress using update [[#Projects|Project Wiki pages]]&lt;br /&gt;
** noon lunch boxes and adjourn.  (Next one [[AHM_2009| in Utah the week of Jan 5, 2009]])&lt;br /&gt;
&lt;br /&gt;
== Preparation ==&lt;br /&gt;
&lt;br /&gt;
# Please make sure that you are on the http://public.kitware.com/cgi-bin/mailman/listinfo/na-mic-project-week mailing list&lt;br /&gt;
&lt;br /&gt;
# [[Engineering:TCON_2008|May 08 and May 15 TCON DBPs ONLY]] at 3pm ET to discuss NA-MIC DBP Projects ONLY. &lt;br /&gt;
# [[Engineering:TCON_2008|May 22 TCON#1]] at 3pm ET to discuss NA-MIC Engr Core Projects and Assign/Verify Teams&lt;br /&gt;
# [[Engineering:TCON_2008|May 29 TCON#2]] at 3pm ET to discuss NA-MIC ALGORITHMS Core Lead Projects.  Project leads should sign up for a slot [[Engineering:TCON_2008|here]]. Projects will be discussed in order of the signups. &lt;br /&gt;
# [[Engineering:TCON_2008|June 5 TCON#3]] at 3pm ET to discuss NA-MIC EXTERNAL Collaborations.  All NIH funded &amp;quot;collaborations with NCBC&amp;quot; leads should call. Project leads should sign up for a slot [[Engineering:TCON_2008|here]].  Projects will be discussed in order of the signups. &lt;br /&gt;
# [[Engineering:TCON_2008|June 12 TCON#4]] at 3pm ET to discuss NA-MIC EXTERNAL Collaborations.  All other collaboration leads should call. Project leads should sign up for a slot [[Engineering:TCON_2008|here]].  Projects will be discussed in order of the signups. &lt;br /&gt;
# [[Engineering:TCON_2008|June 19 TCON#5]] at 3pm ET to tie loose ends.  Anyone with un-addressed questions should call.&lt;br /&gt;
# By 3pm ET on June 12, 2008: [[NA-MIC/Projects/Theme/Template|Complete a templated wiki page for your project]]. Please do not edit the template page itself, but create a new page for your project and cut-and-paste the text from this template page.  If you have questions, please send an email to tkapur at bwh.harvard.edu.&lt;br /&gt;
# By 3pm on June 19, 2008: Create a directory for each project on the [[Engineering:SandBox|NAMIC Sandbox]] (Zack)&lt;br /&gt;
## Commit on each sandbox directory the code examples/snippets that represent our first guesses of appropriate methods. (Luis and Steve will help with this, as needed)&lt;br /&gt;
## Gather test images in any of the Data sharing resources we have (e.g. the BIRN). These ones don't have to be many. At least three different cases, so we can get an idea of the modality-specific characteristics of these images. Put the IDs of these data sets on the wiki page. (the participants must do this.)&lt;br /&gt;
## Setup nightly tests on a separate Dashboard, where we will run the methods that we are experimenting with. The test should post result images and computation time. (Zack)&lt;br /&gt;
# Please note that by the time we get to the project event, we should be trying to close off a project milestone rather than starting to work on one...&lt;br /&gt;
&lt;br /&gt;
== A History in Wiki Links ==&lt;br /&gt;
&lt;br /&gt;
A history of all the programming/project events in NA-MIC is available by following [[Engineering:Programming_Events|this link]].&lt;br /&gt;
&lt;br /&gt;
== Projects ==&lt;br /&gt;
&lt;br /&gt;
===DBP II===&lt;br /&gt;
These are projects by the new set of DBPS:&lt;br /&gt;
#[[DBP2:Harvard|Velocardio Facial Syndrome (VCFS) as a Genetic Model for Schizophrenia]] (Harvard: Marek Kubicki, PI)&lt;br /&gt;
##Add Projects for this DBP here...&lt;br /&gt;
#[[DBP2:UNC|Longitudinal MRI Study of Early Brain Development in Autism]] (UNC: Heather Hazlett, Joseph Piven, PI)&lt;br /&gt;
##Add Projects for this DBP here...&lt;br /&gt;
#[[DBP2:MIND|Analysis of Brain Lesions in Lupus]] (MIND/UNM: Jeremy Bockholt, Charles Gasparovic PI)&lt;br /&gt;
##Add Projects for this DBP here...&lt;br /&gt;
#[[DBP2:JHU|Segmentation and Registration Tools for Robotic Prostate Intervention]] (Queens/JHU: Gabor Fichtinger, PI)&lt;br /&gt;
##Add Projects for this DBP here...&lt;br /&gt;
&lt;br /&gt;
===Structural Analysis===&lt;br /&gt;
&lt;br /&gt;
===Diffusion Image Analysis===&lt;br /&gt;
&lt;br /&gt;
===Calibration/Validation===&lt;br /&gt;
&lt;br /&gt;
===NA-MIC Kit - Slicer 3===&lt;br /&gt;
&lt;br /&gt;
===External Collaborations===&lt;br /&gt;
#[[NA-MIC/Projects/Collaboration/UWA-Perth]] (Adam Wittek)&lt;br /&gt;
#[[NA-MIC/Projects/Collaboration/MRSI Module for Slicer]] (Bjoern Menze)&lt;br /&gt;
&lt;br /&gt;
===Non-Medical Collaborations===&lt;br /&gt;
&lt;br /&gt;
==Attendee List==&lt;br /&gt;
# Ron Kikinis, BWH&lt;br /&gt;
# Gary Christensen, The University of Iowa&lt;br /&gt;
# Jeffrey Hawley, Gary Christensen's student&lt;br /&gt;
# Kate Raising, Gary Christensen's student&lt;br /&gt;
# Nathan Fritze, Gary Christensen's student&lt;br /&gt;
# Paul Song, Gary Christensen's student&lt;br /&gt;
# Cheng Zhang, Gary Christensen's student&lt;br /&gt;
# Ying Wei, Gary Christensen's student&lt;br /&gt;
# Nathan Burnette, The University of Iowa&lt;br /&gt;
# Steve Pieper, Isomics, Core 2/6&lt;br /&gt;
# Dana C. Peters, BIDMC Harvard Medical&lt;br /&gt;
# Jason Taclas, BIDMC Harvard Medical&lt;br /&gt;
# Nicole Aucoin, BWH, Core 2&lt;br /&gt;
# Will Schroeder, Kitware, Cores 2/4&lt;br /&gt;
# Sebastien Barre, Kitware, Core 2&lt;br /&gt;
# Julien Jomier, Kitware, Core 2&lt;br /&gt;
# Curtis Lisle, KnowledgeVis, Core 2&lt;br /&gt;
# Katie Hayes, BWH, Core 2&lt;br /&gt;
# Randy Gollub, MGH, Core 5&lt;br /&gt;
# Clement Vachet, UNC, Core 3&lt;br /&gt;
# Casey Goodlett, Utah, Core 1&lt;br /&gt;
# Tauseef Rehman, GA Tech, Core 1&lt;br /&gt;
# Jeffrey Grethe, UCSD, Core 2&lt;br /&gt;
# Marco Ruiz, UCSD, Core 2&lt;br /&gt;
# Zhen Qian, Rutgers University&lt;br /&gt;
# Jinghao Zhou, Rutgers University&lt;br /&gt;
# Luca Antiga, Mario Negri Institute&lt;br /&gt;
# Adam Wittek, The University of Western Australia&lt;br /&gt;
# Grand Joldes, The University of Western Australia&lt;br /&gt;
# Jamie Berger, The University of Western Australia&lt;br /&gt;
# Serdar Balci, MIT, Core 1&lt;br /&gt;
# Bryce Kim, MIT, Core1&lt;br /&gt;
# Vincent Magnotta, The University of Iowa&lt;br /&gt;
# Tina Kapur, BWH, Core 6&lt;br /&gt;
# Carling Cheung, Robarts Research Institute / The University of Western Ontario&lt;br /&gt;
# Danielle Pace, Robarts Research Institute / The University of Western Ontario&lt;br /&gt;
# Sean Megason, Dept of Systems Biology, Harvard Medical School&lt;br /&gt;
# Alex Gouaillard, Dept of Systems Biology, Harvard Medical School&lt;br /&gt;
# Kishore Mosaliganti, Dept of Systems Biology, Harvard Medical School&lt;br /&gt;
# Arnaud Gelas, Dept of Systems Biology, Harvard Medical School&lt;br /&gt;
# Sonia Pujol, Surgical Planning Laboratory, BWH&lt;br /&gt;
# Bjoern Menze, (then) Surgical Planning Laboratory, BWH&lt;br /&gt;
# Alex Yarmarkovich, Isomics, Core 2&lt;br /&gt;
&lt;br /&gt;
==Pictures==&lt;/div&gt;</summary>
		<author><name>Ybkim</name></author>
		
	</entry>
</feed>