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dc.contributor.authorChang, Hsun-Hsien
dc.contributor.authorMcGeachie, Michael John
dc.contributor.authorAlterovitz, Gil
dc.contributor.authorRamoni, Marco F.
dc.date.accessioned2012-03-09T18:26:40Z
dc.date.available2012-03-09T18:26:40Z
dc.date.issued2010-10
dc.identifier.issn1471-2105
dc.identifier.urihttp://hdl.handle.net/1721.1/69630
dc.description.abstractBackground Identification of expression quantitative trait loci (eQTLs) is an emerging area in genomic study. The task requires an integrated analysis of genome-wide single nucleotide polymorphism (SNP) data and gene expression data, raising a new computational challenge due to the tremendous size of data. Results We develop a method to identify eQTLs. The method represents eQTLs as information flux between genetic variants and transcripts. We use information theory to simultaneously interrogate SNP and gene expression data, resulting in a Transcriptional Information Map (TIM) which captures the network of transcriptional information that links genetic variations, gene expression and regulatory mechanisms. These maps are able to identify both cis- and trans- regulating eQTLs. The application on a dataset of leukemia patients identifies eQTLs in the regions of the GART, PCP4, DSCAM, and RIPK4 genes that regulate ADAMTS1, a known leukemia correlate. Conclusions The information theory approach presented in this paper is able to infer the dependence networks between SNPs and transcripts, which in turn can identify cis- and trans-eQTLs. The application of our method to the leukemia study explains how genetic variants and gene expression are linked to leukemia.en_US
dc.description.sponsorshipNational Human Genome Research Institute (U.S.) (R01HG003354)en_US
dc.description.sponsorshipNational Institute of Allergy and Infectious Diseases (U.S.) (U19 AI067854-05)en_US
dc.description.sponsorshipNational Heart, Lung, and Blood Institute (grant T32 HL007427-28)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (grant K99 LM009826)en_US
dc.language.isoen_US
dc.publisherSpringer (Biomed Central Ltd.)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1186/1471-2105-11-s9-s2en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by/2.0en_US
dc.sourceBioMed Centralen_US
dc.titleMapping transcription mechanisms from multimodal genomic dataen_US
dc.typeArticleen_US
dc.identifier.citationChang, Hsun-Hsien et al. “Mapping Transcription Mechanisms from Multimodal Genomic Data.” BMC Bioinformatics 11.Suppl 9 (2010): S2. Web. 9 Mar. 2012.en_US
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technologyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Computer Science and Artificial Intelligence Laboratoryen_US
dc.contributor.approverAlterovitz, Gil
dc.contributor.mitauthorChang, Hsun-Hsien
dc.contributor.mitauthorMcGeachie, Michael John
dc.contributor.mitauthorAlterovitz, Gil
dc.contributor.mitauthorRamoni, Marco F.
dc.relation.journalBMC Bioinformaticsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsChang, Hsun-Hsien; McGeachie, Michael; Alterovitz, Gil; Ramoni, Marco Fen
dc.identifier.orcidhttps://orcid.org/0000-0002-5952-9844
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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