A Simple and Computationally Efficient Sampling Approach to Covariate Adjustment for Multifactor Dimensionality Reduction Analysis of Epistasis

被引:20
作者
Gui, Jiang [3 ]
Andrew, Angeline S. [3 ]
Andrews, Peter [1 ,2 ]
Nelson, Heather M. [9 ]
Kelsey, Karl T. [7 ]
Karagas, Margaret R. [3 ]
Moore, Jason H. [1 ,2 ,3 ,4 ,5 ,6 ,8 ]
机构
[1] Dartmouth Med Sch, Computat Genet Lab, Norris Cotton Canc Ctr, Lebanon, NH 03756 USA
[2] Dartmouth Med Sch, Dept Genet, Norris Cotton Canc Ctr, Lebanon, NH 03756 USA
[3] Dartmouth Med Sch, Dept Community & Family Med, Norris Cotton Canc Ctr, Lebanon, NH 03756 USA
[4] Univ New Hampshire, Dept Comp Sci, Durham, NH 03824 USA
[5] Univ Vermont, Dept Comp Sci, Burlington, VT USA
[6] Brown Univ, Dept Psychiat & Human Behav, Providence, RI 02912 USA
[7] Brown Univ, Dept Community Hlth, Providence, RI 02912 USA
[8] Translat Genom Res Inst, Phoenix, AZ USA
[9] Univ Minnesota, Sch Publ Hlth, Div Epidemiol & Community Hlth, Minneapolis, MN USA
关键词
Covariate adjustment; Multifactor dimensionality reduction; Epistasis; GENE-GENE INTERACTIONS;
D O I
10.1159/000319175
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Epistasis or gene-gene interaction is a fundamental component of the genetic architecture of complex traits such as disease susceptibility. Multifactor dimensionality reduction (MDR) was developed as a nonparametric and model-free method to detect epistasis when there are no significant marginal genetic effects. However, in many studies of complex disease, other covariates like age of onset and smoking status could have a strong main effect and may potentially interfere with MDR's ability to achieve its goal. In this paper, we present a simple and computationally efficient sampling method to adjust for covariate effects in MDR. We use simulation to show that after adjustment, MDR has sufficient power to detect true gene-gene interactions. We also compare our method with the state-of-art technique in covariate adjustment. The results suggest that our proposed method performs similarly, but is more computationally efficient. We then apply this new method to an analysis of a population-based bladder cancer study in New Hampshire. Copyright (C) 2010 S. Karger AG, Basel
引用
收藏
页码:219 / 225
页数:7
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