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Mapping transcription mechanisms from multimodal genomic data
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...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2967743/ https://www.ncbi.nlm.nih.gov/pubmed/21044360 http://dx.doi.org/10.1186/1471-2105-11-S9-S2 |
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author | Chang, Hsun-Hsien McGeachie, Michael Alterovitz, Gil Ramoni, Marco F |
author_facet | Chang, Hsun-Hsien McGeachie, Michael Alterovitz, Gil Ramoni, Marco F |
author_sort | Chang, Hsun-Hsien |
collection | PubMed |
description | 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. |
format | Text |
id | pubmed-2967743 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29677432010-11-03 Mapping transcription mechanisms from multimodal genomic data Chang, Hsun-Hsien McGeachie, Michael Alterovitz, Gil Ramoni, Marco F BMC Bioinformatics Proceedings 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. BioMed Central 2010-10-28 /pmc/articles/PMC2967743/ /pubmed/21044360 http://dx.doi.org/10.1186/1471-2105-11-S9-S2 Text en Copyright ©2010 Chang et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Proceedings Chang, Hsun-Hsien McGeachie, Michael Alterovitz, Gil Ramoni, Marco F Mapping transcription mechanisms from multimodal genomic data |
title | Mapping transcription mechanisms from multimodal genomic data |
title_full | Mapping transcription mechanisms from multimodal genomic data |
title_fullStr | Mapping transcription mechanisms from multimodal genomic data |
title_full_unstemmed | Mapping transcription mechanisms from multimodal genomic data |
title_short | Mapping transcription mechanisms from multimodal genomic data |
title_sort | mapping transcription mechanisms from multimodal genomic data |
topic | Proceedings |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2967743/ https://www.ncbi.nlm.nih.gov/pubmed/21044360 http://dx.doi.org/10.1186/1471-2105-11-S9-S2 |
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