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dc.contributor.authorCho, Michael
dc.contributor.authorJose, Raul San
dc.contributor.authorGolland, Polina
dc.contributor.authorBatmanghelich, Nematollah Kayhan
dc.date.accessioned2015-12-14T03:12:19Z
dc.date.available2015-12-14T03:12:19Z
dc.date.issued2014
dc.identifier.isbn978-3-319-12288-5
dc.identifier.isbn978-3-319-12289-2
dc.identifier.issn0302-9743
dc.identifier.issn1611-3349
dc.identifier.urihttp://hdl.handle.net/1721.1/100233
dc.description.abstractIn this paper, we use Spherical Topic Models to discover the latent structure of lung disease. This method can be widely employed when a measurement for each subject is provided as a normalized histogram of relevant features. In this paper, the resulting descriptors are used as phenotypes to identify genetic markers associated with the Chronic Obstructive Pulmonary Disease (COPD). Features extracted from images capture the heterogeneity of the disease and therefore promise to improve detection of relevant genetic variants in Genome Wide Association Studies (GWAS). Our generative model is based on normalized histograms of image intensity of each subject and it can be readily extended to other forms of features as long as they are provided as normalized histograms. The resulting algorithm represents the intensity distribution as a combination of meaningful latent factors and mixing coefficients that can be used for genetic association analysis. This approach is motivated by a clinical hypothesis that COPD symptoms are caused by multiple coexisting disease processes. Our experiments show that the new features enhance the previously detected signal on chromosome 15 with respect to standard respiratory and imaging measurements.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (National Institute for Biomedical Imaging and Bioengineering (U.S.)/National Alliance for Medical Image Computing (U.S.) U54-EB005149)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (National Center for Research Resources (U.S.)/Neuroimaging Analysis Center (U.S.) P41-RR13218)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (National Institute for Biomedical Imaging and Bioengineering (U.S.)/Neuroimaging Analysis Center (U.S.) P41-EB-015902)en_US
dc.description.sponsorshipNational Heart, Lung, and Blood Institute (R01HL089856)en_US
dc.description.sponsorshipNational Heart, Lung, and Blood Institute (R01HL089897)en_US
dc.description.sponsorshipNational Heart, Lung, and Blood Institute (K08HL097029)en_US
dc.description.sponsorshipNational Heart, Lung, and Blood Institute (R01HL113264)en_US
dc.language.isoen_US
dc.publisherSpringer-Verlagen_US
dc.relation.isversionofhttp://dx.doi.org/10.1007/978-3-319-12289-2_10en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourcePMCen_US
dc.titleSpherical Topic Models for Imaging Phenotype Discovery in Genetic Studiesen_US
dc.typeArticleen_US
dc.identifier.citationBatmanghelich, Kayhan N., Michael Cho, Raul San Jose, and Polina Golland. “Spherical Topic Models for Imaging Phenotype Discovery in Genetic Studies.” Lecture Notes in Computer Science (2014): 107–117.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Computer Science and Artificial Intelligence Laboratoryen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Electrical Engineering and Computer Scienceen_US
dc.contributor.mitauthorBatmanghelich, Nematollah Kayhanen_US
dc.contributor.mitauthorGolland, Polinaen_US
dc.relation.journalBayesian and grAphical Models for Biomedical Imagingen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsBatmanghelich, Kayhan N.; Cho, Michael; Jose, Raul San; Golland, Polinaen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-1164-0500
dc.identifier.orcidhttps://orcid.org/0000-0003-2516-731X
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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