<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-09-19T16:35:39Z</responseDate><request verb="GetRecord" identifier="oai:dspace.mit.edu:1721.1/66810" metadataPrefix="dim">https://dspace.mit.edu/server/oai/request</request><GetRecord><record><header><identifier>oai:dspace.mit.edu:1721.1/66810</identifier><datestamp>2022-01-13T07:54:29Z</datestamp><setSpec>com_1721.1_7582</setSpec><setSpec>com_1721.1_7581</setSpec><setSpec>col_1721.1_131023</setSpec></header><metadata><dim:dim xmlns:dim="http://www.dspace.org/xmlns/dspace/dim" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.dspace.org/xmlns/dspace/dim http://www.dspace.org/schema/dim.xsd">
   <dim:field mdschema="dc" element="contributor" qualifier="advisor" lang="en_US">Polina Golland.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author" lang="en_US">Tobón, Gabriel Andres</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="other" lang="en_US">Massachusetts Institute of Technology. Dept. of Electrical Engineering and Computer Science.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="department">Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="accessioned">2011-11-01T19:47:37Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2011-11-01T19:47:37Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="copyright" lang="en_US">2011</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="issued" lang="en_US">2011</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">http://hdl.handle.net/1721.1/66810</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="oclc" lang="en_US">757169317</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Thesis (M. Eng.)--Massachusetts Institute of Technology, Dept. of Electrical Engineering and Computer Science, 2011.</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Cataloged from PDF version of thesis.</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Includes bibliographical references (p. 49-50).</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">An essential step for discovering a common structure in brain activation regions from multi-subject fMRI data is the ability to find spatial correspondences across subjects. This has proven to be a challenging problem due to the lack of a ground truth and variability in anatomical brain structure, functional activation, and spatial locations of functional regions. Standard methods rely on the correspondences given by anatomical registration to a common space, but fail to account for spatial variability of the functional regions relative to anatomy. We develop a clustering method that relies on the alignment of both the anatomical structure and the functional landmarks. The method is shown to improve over standard group analysis techniques that rely on anatomical alignment only. The validation of our method confirms that peaks of activation exhibit consistent spatial structure. Furthermore, our work creates a framework for future testing of different metrics for similarity of brain activation regions across subjects.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="statementofresponsibility" lang="en_US">by Gabriel Andres Tobón.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="degree" lang="en_US">M.Eng.</dim:field>
   <dim:field mdschema="dc" element="format" qualifier="extent" lang="en_US">50 p.</dim:field>
   <dim:field mdschema="dc" element="language" qualifier="iso" lang="en_US">eng</dim:field>
   <dim:field mdschema="dc" element="publisher" lang="en_US">Massachusetts Institute of Technology</dim:field>
   <dim:field mdschema="dc" element="rights" lang="en_US">M.I.T. theses are protected by 
copyright. They may be viewed from this source for any purpose, but 
reproduction or distribution in any format is prohibited without written 
permission. See provided URL for inquiries about permission.</dim:field>
   <dim:field mdschema="dc" element="rights" qualifier="uri" lang="en_US">http://dspace.mit.edu/handle/1721.1/7582</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">Electrical Engineering and Computer Science.</dim:field>
   <dim:field mdschema="dc" element="title" lang="en_US">Spatial alignment of functional regions in fMRI</dim:field>
   <dim:field mdschema="dc" element="title" qualifier="alternative" lang="en_US">Spatial modeling of functional regions of interest in fMRI group analysis</dim:field>
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	&lt;Language>eng&lt;/Language>
   	&lt;Title>Spatial alignment of functional regions in fMRI&lt;/Title>
   	&lt;Subtitle>Spatial modeling of functional regions of interest in fMRI group analysis&lt;/Subtitle>
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   	&lt;PublicationDate>2011&lt;/PublicationDate>
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        	&lt;DisplayName>Tobón, Gabriel Andres&lt;/DisplayName>
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            &lt;DisplayName>Massachusetts Institute of Technology&lt;/DisplayName>
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    &lt;License>http://dspace.mit.edu/handle/1721.1/7582&lt;/License>
    &lt;Keyword>Electrical Engineering and Computer Science.&lt;/Keyword>
   	&lt;Abstract>An essential step for discovering a common structure in brain activation regions from multi-subject fMRI data is the ability to find spatial correspondences across subjects. This has proven to be a challenging problem due to the lack of a ground truth and variability in anatomical brain structure, functional activation, and spatial locations of functional regions. Standard methods rely on the correspondences given by anatomical registration to a common space, but fail to account for spatial variability of the functional regions relative to anatomy. We develop a clustering method that relies on the alignment of both the anatomical structure and the functional landmarks. The method is shown to improve over standard group analysis techniques that rely on anatomical alignment only. The validation of our method confirms that peaks of activation exhibit consistent spatial structure. Furthermore, our work creates a framework for future testing of different metrics for similarity of brain activation regions across subjects.&lt;/Abstract>
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