Semiparametric Bayesian variable selection for gene-environment interactions

被引:16
|
作者
Ren, Jie [1 ]
Zhou, Fei [1 ]
Li, Xiaoxi [1 ]
Chen, Qi [2 ]
Zhang, Hongmei [3 ]
Ma, Shuangge [4 ]
Jiang, Yu [3 ]
Wu, Cen [1 ]
机构
[1] Kansas State Univ, Dept Stat, Manhattan, KS 66506 USA
[2] Univ Kansas, Med Ctr, Dept Pharmacol Toxicol & Therapeut, Kansas City, KS 66103 USA
[3] Univ Memphis, Sch Publ Hlth, Div Epidemiol Biostat & Environm Hlth, Memphis, TN 38152 USA
[4] Yale Univ, Dept Biostat, New Haven, CT USA
基金
美国国家卫生研究院;
关键词
Bayesian variable selection; gene-environment interactions; high-dimensional genomic data; MCMC; semiparametric modeling; VARYING-COEFFICIENT MODELS; GENOME-WIDE ASSOCIATION; REGRESSION; LASSO;
D O I
10.1002/sim.8434
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Many complex diseases are known to be affected by the interactions between genetic variants and environmental exposures beyond the main genetic and environmental effects. Study of gene-environment (GxE) interactions is important for elucidating the disease etiology. Existing Bayesian methods for GxE interaction studies are challenged by the high-dimensional nature of the study and the complexity of environmental influences. Many studies have shown the advantages of penalization methods in detecting GxE interactions in "large p, small n" settings. However, Bayesian variable selection, which can provide fresh insight into GxE study, has not been widely examined. We propose a novel and powerful semiparametric Bayesian variable selection model that can investigate linear and nonlinear GxE interactions simultaneously. Furthermore, the proposed method can conduct structural identification by distinguishing nonlinear interactions from main-effects-only case within the Bayesian framework. Spike-and-slab priors are incorporated on both individual and group levels to identify the sparse main and interaction effects. The proposed method conducts Bayesian variable selection more efficiently than existing methods. Simulation shows that the proposed model outperforms competing alternatives in terms of both identification and prediction. The proposed Bayesian method leads to the identification of main and interaction effects with important implications in a high-throughput profiling study with high-dimensional SNP data.
引用
收藏
页码:617 / 638
页数:22
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