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A Statistical Framework for Joint eQTL Analysis in Multiple Tissues
Mapping expression Quantitative Trait Loci (eQTLs) represents a powerful and widely adopted approach to identifying putative regulatory variants and linking them to specific genes. Up to now eQTL studies have been conducted in a relatively narrow range of tissues or cell types. However, understandin...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3649995/ https://www.ncbi.nlm.nih.gov/pubmed/23671422 http://dx.doi.org/10.1371/journal.pgen.1003486 |
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author | Flutre, Timothée Wen, Xiaoquan Pritchard, Jonathan Stephens, Matthew |
author_facet | Flutre, Timothée Wen, Xiaoquan Pritchard, Jonathan Stephens, Matthew |
author_sort | Flutre, Timothée |
collection | PubMed |
description | Mapping expression Quantitative Trait Loci (eQTLs) represents a powerful and widely adopted approach to identifying putative regulatory variants and linking them to specific genes. Up to now eQTL studies have been conducted in a relatively narrow range of tissues or cell types. However, understanding the biology of organismal phenotypes will involve understanding regulation in multiple tissues, and ongoing studies are collecting eQTL data in dozens of cell types. Here we present a statistical framework for powerfully detecting eQTLs in multiple tissues or cell types (or, more generally, multiple subgroups). The framework explicitly models the potential for each eQTL to be active in some tissues and inactive in others. By modeling the sharing of active eQTLs among tissues, this framework increases power to detect eQTLs that are present in more than one tissue compared with “tissue-by-tissue” analyses that examine each tissue separately. Conversely, by modeling the inactivity of eQTLs in some tissues, the framework allows the proportion of eQTLs shared across different tissues to be formally estimated as parameters of a model, addressing the difficulties of accounting for incomplete power when comparing overlaps of eQTLs identified by tissue-by-tissue analyses. Applying our framework to re-analyze data from transformed B cells, T cells, and fibroblasts, we find that it substantially increases power compared with tissue-by-tissue analysis, identifying 63% more genes with eQTLs (at FDR = 0.05). Further, the results suggest that, in contrast to previous analyses of the same data, the majority of eQTLs detectable in these data are shared among all three tissues. |
format | Online Article Text |
id | pubmed-3649995 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-36499952013-05-13 A Statistical Framework for Joint eQTL Analysis in Multiple Tissues Flutre, Timothée Wen, Xiaoquan Pritchard, Jonathan Stephens, Matthew PLoS Genet Research Article Mapping expression Quantitative Trait Loci (eQTLs) represents a powerful and widely adopted approach to identifying putative regulatory variants and linking them to specific genes. Up to now eQTL studies have been conducted in a relatively narrow range of tissues or cell types. However, understanding the biology of organismal phenotypes will involve understanding regulation in multiple tissues, and ongoing studies are collecting eQTL data in dozens of cell types. Here we present a statistical framework for powerfully detecting eQTLs in multiple tissues or cell types (or, more generally, multiple subgroups). The framework explicitly models the potential for each eQTL to be active in some tissues and inactive in others. By modeling the sharing of active eQTLs among tissues, this framework increases power to detect eQTLs that are present in more than one tissue compared with “tissue-by-tissue” analyses that examine each tissue separately. Conversely, by modeling the inactivity of eQTLs in some tissues, the framework allows the proportion of eQTLs shared across different tissues to be formally estimated as parameters of a model, addressing the difficulties of accounting for incomplete power when comparing overlaps of eQTLs identified by tissue-by-tissue analyses. Applying our framework to re-analyze data from transformed B cells, T cells, and fibroblasts, we find that it substantially increases power compared with tissue-by-tissue analysis, identifying 63% more genes with eQTLs (at FDR = 0.05). Further, the results suggest that, in contrast to previous analyses of the same data, the majority of eQTLs detectable in these data are shared among all three tissues. Public Library of Science 2013-05-09 /pmc/articles/PMC3649995/ /pubmed/23671422 http://dx.doi.org/10.1371/journal.pgen.1003486 Text en © 2013 Flutre et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Flutre, Timothée Wen, Xiaoquan Pritchard, Jonathan Stephens, Matthew A Statistical Framework for Joint eQTL Analysis in Multiple Tissues |
title | A Statistical Framework for Joint eQTL Analysis in Multiple Tissues |
title_full | A Statistical Framework for Joint eQTL Analysis in Multiple Tissues |
title_fullStr | A Statistical Framework for Joint eQTL Analysis in Multiple Tissues |
title_full_unstemmed | A Statistical Framework for Joint eQTL Analysis in Multiple Tissues |
title_short | A Statistical Framework for Joint eQTL Analysis in Multiple Tissues |
title_sort | statistical framework for joint eqtl analysis in multiple tissues |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3649995/ https://www.ncbi.nlm.nih.gov/pubmed/23671422 http://dx.doi.org/10.1371/journal.pgen.1003486 |
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