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FLAGS: A Flexible and Adaptive Association Test for Gene Sets Using Summary Statistics
Author(s) -
Jianfei Huang,
Kai Wang,
Peng Wei,
Xiangtao Liu,
Xiaoming Liu,
Kai Tan,
Eric Boerwinkle,
James B. Potash,
Shizhong Han
Publication year - 2016
Publication title -
genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.792
H-Index - 246
eISSN - 1943-2631
pISSN - 0016-6731
DOI - 10.1534/genetics.115.185009
Subject(s) - genome wide association study , genetic association , biology , missing heritability problem , computational biology , heritability , set (abstract data type) , association (psychology) , type i and type ii errors , summary statistics , genetics , computer science , statistics , gene , single nucleotide polymorphism , genotype , mathematics , philosophy , epistemology , programming language
Genome-wide association studies (GWAS) have been widely used for identifying common variants associated with complex diseases. Despite remarkable success in uncovering many risk variants and providing novel insights into disease biology, genetic variants identified to date fail to explain the vast majority of the heritability for most complex diseases. One explanation is that there are still a large number of common variants that remain to be discovered, but their effect sizes are generally too small to be detected individually. Accordingly, gene set analysis of GWAS, which examines a group of functionally related genes, has been proposed as a complementary approach to single-marker analysis. Here, we propose a FL: exible and A: daptive test for G: ene S: ets (FLAGS), using summary statistics. Extensive simulations showed that this method has an appropriate type I error rate and outperforms existing methods with increased power. As a proof of principle, through real data analyses of Crohn's disease GWAS data and bipolar disorder GWAS meta-analysis results, we demonstrated the superior performance of FLAGS over several state-of-the-art association tests for gene sets. Our method allows for the more powerful application of gene set analysis to complex diseases, which will have broad use given that GWAS summary results are increasingly publicly available.

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