| dc.contributor.author | Chang, Hsun-Hsien | |
| dc.contributor.author | McGeachie, Michael John | |
| dc.contributor.author | Alterovitz, Gil | |
| dc.contributor.author | Ramoni, Marco F. | |
| dc.date.accessioned | 2012-03-09T18:26:40Z | |
| dc.date.available | 2012-03-09T18:26:40Z | |
| dc.date.issued | 2010-10 | |
| dc.identifier.issn | 1471-2105 | |
| dc.identifier.uri | http://hdl.handle.net/1721.1/69630 | |
| dc.description.abstract | Background
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.sponsorship | National Human Genome Research Institute (U.S.) (R01HG003354) | en_US |
| dc.description.sponsorship | National Institute of Allergy and Infectious Diseases (U.S.) (U19 AI067854-05) | en_US |
| dc.description.sponsorship | National Heart, Lung, and Blood Institute (grant T32 HL007427-28) | en_US |
| dc.description.sponsorship | National Institutes of Health (U.S.) (grant K99 LM009826) | en_US |
| dc.language.iso | en_US | |
| dc.publisher | Springer (Biomed Central Ltd.) | en_US |
| dc.relation.isversionof | http://dx.doi.org/10.1186/1471-2105-11-s9-s2 | en_US |
| dc.rights | Creative Commons Attribution | en_US |
| dc.rights.uri | http://creativecommons.org/licenses/by/2.0 | en_US |
| dc.source | BioMed Central | en_US |
| dc.title | Mapping transcription mechanisms from multimodal genomic data | en_US |
| dc.type | Article | en_US |
| dc.identifier.citation | Chang, 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.department | Harvard University--MIT Division of Health Sciences and Technology | en_US |
| dc.contributor.department | Massachusetts Institute of Technology. Computer Science and Artificial Intelligence Laboratory | en_US |
| dc.contributor.approver | Alterovitz, Gil | |
| dc.contributor.mitauthor | Chang, Hsun-Hsien | |
| dc.contributor.mitauthor | McGeachie, Michael John | |
| dc.contributor.mitauthor | Alterovitz, Gil | |
| dc.contributor.mitauthor | Ramoni, Marco F. | |
| dc.relation.journal | BMC Bioinformatics | en_US |
| dc.eprint.version | Final published version | en_US |
| dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
| eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
| dspace.orderedauthors | Chang, Hsun-Hsien; McGeachie, Michael; Alterovitz, Gil; Ramoni, Marco F | en |
| dc.identifier.orcid | https://orcid.org/0000-0002-5952-9844 | |
| mit.license | PUBLISHER_CC | en_US |
| mit.metadata.status | Complete | |