HT-eQTL: integrative expression quantitative trait loci analysis in a large number of human tissues

被引:10
|
作者
Li, Gen [1 ]
Jima, Dereje [2 ]
Wright, Fred A. [2 ,3 ,4 ]
Nobel, Andrew B. [5 ,6 ]
机构
[1] Columbia Univ, Mailman Sch Publ Hlth, Dept Biostat, 722 W 168 St, New York, NY 10027 USA
[2] North Carolina State Univ, Ctr Human Hlth & Environm, 850 Main Campus Dr, Raleigh, NC 27695 USA
[3] North Carolina State Univ, Bioinformat Res Ctr, 850 Main Campus Dr, Raleigh, NC 27695 USA
[4] North Carolina State Univ, Dept Stat & Biol Sci, 2311 Stinson Dr, Raleigh, NC 27695 USA
[5] Univ N Carolina, Dept Stat & Operat Res, 318 E Cameron Ave, Chapel Hill, NC 27599 USA
[6] Univ N Carolina, Dept Biostat, 318 E Cameron Ave, Chapel Hill, NC 27599 USA
来源
BMC BIOINFORMATICS | 2018年 / 19卷
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
Expression quantitative trait loci; Genotype-tissue expression project; Empirical Bayes; Tissue specific; Local false discovery rate; FALSE DISCOVERY RATE; GENE-EXPRESSION; EMPIRICAL BAYES;
D O I
10.1186/s12859-018-2088-3
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页数:11
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