Difference between revisions of "DBP2:MIND:Roadmap"

From NAMIC Wiki
Jump to: navigation, search
Line 2: Line 2:
  
 
==Objective==
 
==Objective==
We would like to create an end-to-end application within NA-MIC Kit allowing individual analysis of white matter lesions. Such a workflow applied to lupus patients is one goals of the MIND DBP. This page describes the technology roadmap for lesion analysis in the NA-MIC Kit. The basic components necessary for this end-to-end application are:
+
We would like to create an end-to-end application within NA-MIC Kit allowing individual analysis of white matter lesions. Such a workflow applied to lupus patients is one of goals of the MIND DBP. This page describes the technology roadmap for lesion analysis in the NA-MIC Kit. The basic components necessary for this application are:
 
* '''Registration''': co-registration of T1-weighted, T2-weighted, and FLAIR images
 
* '''Registration''': co-registration of T1-weighted, T2-weighted, and FLAIR images
 
* '''Tissue segmentation''': Should be multi-modality, correcting for intensity inhomogeneity and work on non-skull-stripped data.
 
* '''Tissue segmentation''': Should be multi-modality, correcting for intensity inhomogeneity and work on non-skull-stripped data.
* '''Lesion Localization''':  Each unique lesion should be detacted and anatomical location summarized  
+
* '''Lesion Localization''':  Each unique lesion should be detected and anatomical location summarized  
 
* '''Lesion Load Measurement''': Measure volume of each lesion, summarize lesion load by regions
 
* '''Lesion Load Measurement''': Measure volume of each lesion, summarize lesion load by regions
 
* '''Tutorial''':  Documentation will be written for a tutorial and sample data sets will be provided
 
* '''Tutorial''':  Documentation will be written for a tutorial and sample data sets will be provided

Revision as of 14:40, 27 September 2007

Home < DBP2:MIND:Roadmap

Brain Lesion Analysis in Neuropsychiatric Systemic Lupus Erythematosus

Objective

We would like to create an end-to-end application within NA-MIC Kit allowing individual analysis of white matter lesions. Such a workflow applied to lupus patients is one of goals of the MIND DBP. This page describes the technology roadmap for lesion analysis in the NA-MIC Kit. The basic components necessary for this application are:

  • Registration: co-registration of T1-weighted, T2-weighted, and FLAIR images
  • Tissue segmentation: Should be multi-modality, correcting for intensity inhomogeneity and work on non-skull-stripped data.
  • Lesion Localization: Each unique lesion should be detected and anatomical location summarized
  • Lesion Load Measurement: Measure volume of each lesion, summarize lesion load by regions
  • Tutorial: Documentation will be written for a tutorial and sample data sets will be provided

Roadmap

Starting with several MRI images (weighted-T1, weighted-T2, FLAIR...) we want to obtain lesion maps for each subject. Ultimately, the NA-MIC Kit will provide a workflow for individual and group analysis of lesions. It will be implemented as a set of Slicer3 modules that can be used interactively within the Slicer3 application as well as in batch on a computing cluster using BatchMake.

Next we discuss the main modules and details of current status and development work:

Registration

  • ITK has mutual information registration
  • BRAINS2 has AIR package wrapped

Lesion segmentation

A number of algorithms for fully or semi-automated lesion analysis will be evaluated on brain images from subjects in a study on lupus erythematosis. These include:

  • UNC has a tool called itkEMS Compare Lesion Analysis Tools (marcel)
  • EM-segment (sandy wells)
  • MedX (commercial package)
  • BRAINS2 (magnotta)
  • manual tracing by clinically trained rater

Lesion Localization

  • Freesurfer has tools for labeling white matter lesions and summarizing their anatomical location
  • BRAINS2 has tools for creating masks for white matter lesions and summarizing their anatomical location

Lesion Load Measurement

  • Freesurfer has tools for measurement of labelled lesions
  • BRAINS2 has tools for measurement of lesions and regional summaries

Performance characterization and validation

  • Data will be collected at both 1.5 and 3T. Data at 1.5T will be obtained with the protocol utilized for current project on lupus at UNM.
  • Data at 3T will be obtained with sequences optimized for segmentation by the group at Utah.
  • Comparisons will be based on the approach developed by Martin-Fernandez et al.
  • The algorithm with the best performance will be incorporated into the NA-MIC kit.

Tutorial

  • 5 Publically sharable T1,T2,Flair,Lesion Map data-sets (NIFTI format) will be made available
  • A tutorial will be created that will guide end-users through each step needed to complete a lesion analysis in the NA-MIC kit

Schedule

  • Sequence Optimization and Data Collection
  • 10/15/2007 T1, T2, FLAIR optimized sequences for Siemens 3T Trio Tim scanner (Jeremy, Bruce, Chuck)
    • we will work with Bruce Fischl on using MEMPR, Mugler, and FLAIR sequences that have been optimized for maximum constrast and minimal geometric distortion across sequences
  • 11/15/2007 collection of 5 lupus subjects on clinical sequence and optimized 3T sequence (Chuck)
  • Registration
  • 10/30/2007 optimized mutual information registration for clinical sequences and optimized 3T sequences (Jeremy)
  • Lesion segmentation
  • 11/30/2007 complete lesion segmentation methods for EM-segment, BRAINS2, manual, MedX, UNC packages (Jeremy, Chuck, Vince Magnotta, Kilian/Brad, Marcel)
  • Lesion Localization
  • 11/30/2007 complete lesion localizations and maps for EM-segment, BRAINS2, manual, MedX, UNC packages (Jeremy, Chuck, Vince Magnotta, Bruce, Steve)
  • Lesion Measurement
  • 11/30/2007 complete lesion measurements and regional lesion load summaries for EM-segment, BRAINS2, manual, MedX, UNC packages (Jeremy, Chuck, Vince Magnotta, Bruce, Steve)
  • Performance characterization and validation
  • 1/6/2008 report to 2008 NA-MIC AHM on performance and validation of lesion segmentation methods for EM-segment, BRAINS2, manual, MedX, UNC packages (Jeremy)
  • 2/15/2008 submit manuscript on reliability and summary of novel NA-MIC kit lesion analysis method (Jeremy, Chuck, Mark Scully)
  • 3/15/2008 analyze NIH study clinical sample using NA-MIC kit lesion analysis method (Jeremy, Chuck, Mark Scully)
  • 4/15/2008 submit manuscript on clinical application of NA-MIC kit lesion analysis method (Jeremy, Chuck, Mark Scully, Carlos Roldan, Bill Sibbitt)
  • Incorporation of approach into NA-MIC kit
  • 11/1/2007 Slicer3 Lesion Analysis Module that handles co-registration of T1, T2, and Flair (Mark Scully, Steve)
  • 12/1/2008 extend Slicer3 Lesion Analysis Module to handle lesion localization and measurement (Mark Scully, Steve)
  • 1/6/2008 extend Slicer3 Lesion Analysis Module to implement the lesion analysis method (EM-segment, BRAINS2, MedX, UNC packages) with the best performance (Mark Scully, Steve)
    • a demonstration will be given at the 2008 NA-MIC AHM--we would consider this version a prototype and would be testing, refining the module through the clinical application phase (Jeremy, Mark Scully)
  • 4/1/2008 production version of lesion analysis Slicer3 Module complete (Mark Scully, Steve)
  • Tutorial and Data-sharing
  • 5/1/2008 make data sets and tutorial publically available (Jeremy, Sonja)

Team and Institute

  • Co-PI: H Jeremy Bockholt (jbockholt at mrn.org)
  • Co-PI: Charles Gasparovic (chuck at unm.edu)
  • Software Engineer: Mark Scully (mscully at mrn .org)
  • NA-MIC Engineering Contact: Steve Pieper, Isomics
  • NA-MIC Algorithms Contact: Bruce Fischl, MGH
  • Consultant: Vincent Magnotta, University of Iowa
  • Host Institues: The MIND Institute and The University of New Mexico