| Literature DB >> 26773050 |
Jianfei Huang1, Kai Wang2, Peng Wei3, Xiangtao Liu1, Xiaoming Liu4, Kai Tan5, Eric Boerwinkle6, James B Potash1, Shizhong Han7.
Abstract
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.Entities:
Keywords: GWAS; association; complex disease; gene set; summary statistics
Mesh:
Year: 2016 PMID: 26773050 PMCID: PMC4788129 DOI: 10.1534/genetics.115.185009
Source DB: PubMed Journal: Genetics ISSN: 0016-6731 Impact factor: 4.562