A penalized robust semiparametric approach for gene-environment interactions

被引:25
|
作者
Wu, Cen [1 ,2 ]
Shi, Xingjie [3 ]
Cui, Yuehua [4 ]
Ma, Shuangge [1 ,5 ]
机构
[1] Yale Univ, Dept Biostat, Sch Publ Hlth, New Haven, CT 06520 USA
[2] Kansas State Univ, Dept Stat, Manhattan, KS 66506 USA
[3] Nanjing Univ Finance & Econ, Dept Stat, Nanjing, Jiangsu, Peoples R China
[4] Michigan State Univ, Dept Stat & Probabil, E Lansing, MI 48824 USA
[5] VA Cooperat Studies Program Coordinating Ctr, West Haven, CT 06516 USA
基金
中国国家自然科学基金;
关键词
gene-environment interactions; robustness; partially linear varying coefficient model; penalized selection; CELL LUNG-CANCER; MODEL SELECTION; EXPRESSION; REGRESSION; CONVERGENCE; ASSOCIATION; PROSTATE; HLA-DQA1; SAMPLES; RISK;
D O I
10.1002/sim.6609
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
In genetic and genomic studies, gene-environment (G x E) interactions have important implications. Some of the existing G x E interaction methods are limited by analyzing a small number of G factors at a time, by assuming linear effects of E factors, by assuming no data contamination, and by adopting ineffective selection techniques. In this study, we propose a new approach for identifying important G x E interactions. It jointly models the effects of all E and G factors and their interactions. A partially linear varying coefficient model is adopted to accommodate possible nonlinear effects of E factors. A rank-based loss function is used to accommodate possible data contamination. Penalization, which has been extensively used with high-dimensional data, is adopted for selection. The proposed penalized estimation approach can automatically determine if a G factor has an interaction with an E factor, main effect but not interaction, or no effect at all. The proposed approach can be effectively realized using a coordinate descent algorithm. Simulation shows that it has satisfactory performance and outperforms several competing alternatives. The proposed approach is used to analyze a lung cancer study with gene expression measurements and clinical variables. Copyright (C) 2015 John Wiley & Sons, Ltd.
引用
收藏
页码:4016 / 4030
页数:15
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