REPLICABILITY ANALYSIS FOR GENOME-WIDE ASSOCIATION STUDIES

被引:34
|
作者
Heller, Ruth [1 ]
Yekutieli, Daniel [1 ]
机构
[1] Tel Aviv Univ, Dept Stat & Operat Res, IL-69978 Tel Aviv, Israel
来源
ANNALS OF APPLIED STATISTICS | 2014年 / 8卷 / 01期
基金
以色列科学基金会;
关键词
Combined analysis; empirical Bayes; false discovery rate; meta-analysis; replication; reproducibility; type; 2; diabetes; FALSE DISCOVERY RATE; EMPIRICAL BAYES; REPLICATION; LOCI;
D O I
10.1214/13-AOAS697
中图分类号
O21 [概率论与数理统计]; C8 [统计学];
学科分类号
020208 ; 070103 ; 0714 ;
摘要
The paramount importance of replicating associations is well recognized in the genome-wide associaton (GWA) research community, yet methods for assessing replicability of associations are scarce. Published GWA studies often combine separately the results of primary studies and of the follow-up studies. Informally, reporting the two separate meta-analyses, that of the primary studies and follow-up studies, gives a sense of the replicability of the results. We suggest a formal empirical Bayes approach for discovering whether results have been replicated across studies, in which we estimate the optimal rejection region for discovering replicated results. We demonstrate, using realistic simulations, that the average false discovery proportion of our method remains small. We apply our method to six type two diabetes (T2D) GWA studies. Out of 803 SNPs discovered to be associated with T2D using a typical meta-analysis, we discovered 219 SNPs with replicated associations with T2D. We recommend complementing a meta-analysis with a replicability analysis for GWA studies.
引用
收藏
页码:481 / 498
页数:18
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