全基因组关联研究
表达数量性状基因座
生物
遗传关联
数量性状位点
因果关系(物理学)
特质
一致性
遗传学
计算生物学
基因
基因型
单核苷酸多态性
计算机科学
物理
量子力学
程序设计语言
作者
Halit Ongen,Andrew Brown,Olivier Delaneau,Nikolaos Panousis,Alexandra C. Nica,Emmanouil T. Dermitzakis
出处
期刊:Nature Genetics
[Springer Nature]
日期:2017-10-23
卷期号:49 (12): 1676-1683
被引量:188
摘要
How to interpret the biological causes underlying the predisposing markers identified through genome-wide association studies (GWAS) remains an open question. One direct and powerful way to assess the genetic causality behind GWAS is through analysis of expression quantitative trait loci (eQTLs). Here we describe a new approach to estimate the tissues behind the genetic causality of a variety of GWAS traits, using the cis-eQTLs in 44 tissues from the Genotype-Tissue Expression (GTEx) Consortium. We have adapted the regulatory trait concordance (RTC) score to measure the probability of eQTLs being active in multiple tissues and to calculate the probability that a GWAS-associated variant and an eQTL tag the same functional effect. By normalizing the GWAS-eQTL probabilities by the tissue-sharing estimates for eQTLs, we generate relative tissue-causality profiles for GWAS traits. Our approach not only implicates the gene likely mediating individual GWAS signals, but also highlights tissues where the genetic causality for an individual trait is likely manifested.
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