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HT-eQTL: integrative expression quantitative trait loci analysis in a large number of human tissues
BACKGROUND: Expression quantitative trait loci (eQTL) analysis identifies genetic markers associated with the expression of a gene. Most existing eQTL analyses and methods investigate association in a single, readily available tissue, such as blood. Joint analysis of eQTL in multiple tissues has the...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5845327/ https://www.ncbi.nlm.nih.gov/pubmed/29523079 http://dx.doi.org/10.1186/s12859-018-2088-3 |
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author | Li, Gen Jima, Dereje Wright, Fred A. Nobel, Andrew B. |
author_facet | Li, Gen Jima, Dereje Wright, Fred A. Nobel, Andrew B. |
author_sort | Li, Gen |
collection | PubMed |
description | BACKGROUND: Expression quantitative trait loci (eQTL) analysis identifies genetic markers associated with the expression of a gene. Most existing eQTL analyses and methods investigate association in a single, readily available tissue, such as blood. Joint analysis of eQTL in multiple tissues has the potential to improve, and expand the scope of, single-tissue analyses. Large-scale collaborative efforts such as the Genotype-Tissue Expression (GTEx) program are currently generating high quality data in a large number of tissues. However, computational constraints limit genome-wide multi-tissue eQTL analysis. RESULTS: We develop an integrative method under a hierarchical Bayesian framework for eQTL analysis in a large number of tissues. The model fitting procedure is highly scalable, and the computing time is a polynomial function of the number of tissues. Multi-tissue eQTLs are identified through a local false discovery rate approach, which rigorously controls the false discovery rate. Using simulation and GTEx real data studies, we show that the proposed method has superior performance to existing methods in terms of computing time and the power of eQTL discovery. CONCLUSIONS: We provide a scalable method for eQTL analysis in a large number of tissues. The method enables the identification of eQTL with different configurations and facilitates the characterization of tissue specificity. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12859-018-2088-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5845327 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-58453272018-03-19 HT-eQTL: integrative expression quantitative trait loci analysis in a large number of human tissues Li, Gen Jima, Dereje Wright, Fred A. Nobel, Andrew B. BMC Bioinformatics Methodology Article BACKGROUND: Expression quantitative trait loci (eQTL) analysis identifies genetic markers associated with the expression of a gene. Most existing eQTL analyses and methods investigate association in a single, readily available tissue, such as blood. Joint analysis of eQTL in multiple tissues has the potential to improve, and expand the scope of, single-tissue analyses. Large-scale collaborative efforts such as the Genotype-Tissue Expression (GTEx) program are currently generating high quality data in a large number of tissues. However, computational constraints limit genome-wide multi-tissue eQTL analysis. RESULTS: We develop an integrative method under a hierarchical Bayesian framework for eQTL analysis in a large number of tissues. The model fitting procedure is highly scalable, and the computing time is a polynomial function of the number of tissues. Multi-tissue eQTLs are identified through a local false discovery rate approach, which rigorously controls the false discovery rate. Using simulation and GTEx real data studies, we show that the proposed method has superior performance to existing methods in terms of computing time and the power of eQTL discovery. CONCLUSIONS: We provide a scalable method for eQTL analysis in a large number of tissues. The method enables the identification of eQTL with different configurations and facilitates the characterization of tissue specificity. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12859-018-2088-3) contains supplementary material, which is available to authorized users. BioMed Central 2018-03-09 /pmc/articles/PMC5845327/ /pubmed/29523079 http://dx.doi.org/10.1186/s12859-018-2088-3 Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Methodology Article Li, Gen Jima, Dereje Wright, Fred A. Nobel, Andrew B. HT-eQTL: integrative expression quantitative trait loci analysis in a large number of human tissues |
title | HT-eQTL: integrative expression quantitative trait loci analysis in a large number of human tissues |
title_full | HT-eQTL: integrative expression quantitative trait loci analysis in a large number of human tissues |
title_fullStr | HT-eQTL: integrative expression quantitative trait loci analysis in a large number of human tissues |
title_full_unstemmed | HT-eQTL: integrative expression quantitative trait loci analysis in a large number of human tissues |
title_short | HT-eQTL: integrative expression quantitative trait loci analysis in a large number of human tissues |
title_sort | ht-eqtl: integrative expression quantitative trait loci analysis in a large number of human tissues |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5845327/ https://www.ncbi.nlm.nih.gov/pubmed/29523079 http://dx.doi.org/10.1186/s12859-018-2088-3 |
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