Detection of gene x gene interactions in genome-wide association studies of human population data

被引:125
作者
Musani, Solomon K.
Shriner, Daniel
Liu, Nianjun
Feng, Rui
Coffey, Christopher S.
Yi, Nengjun
Tiwari, Hemant K.
Allison, David B.
机构
[1] Univ Alabama, Sect Stat Genet, Dept Biostat, Birmingham, AL 35294 USA
[2] Univ Alabama, Sect Res Methods & Clin Trials, Dept Biostat, Birmingham, AL 35294 USA
[3] Univ Alabama, Clin Nutr Res Ctr, Birmingham, AL 35294 USA
关键词
epistasis; genome-wide association; computational burden; overfitting; data sparsity; methodological issues;
D O I
10.1159/000099179
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Empirical evidence supporting the commonality of gene x gene interactions, coupled with frequent failure to replicate results from previous association studies, has prompted statisticians to develop methods to handle this important subject. Nonparametric methods have generated intense interest because of their capacity to handle high-dimensional data. Genome-wide association analysis of large-scale SNP data is challenging mathematically and computationally. In this paper, we describe major issues and questions arising from this challenge, along with methodological implications. Data reduction and pattern recognition methods seem to be the new frontiers in efforts to detect gene x gene interactions comprehensively. Currently, there is no single method that is recognized as the 'best' for detecting, characterizing, and interpreting gene x gene interactions. Instead, a combination of approaches with the aim of balancing their specific strengths may be the optimal approach to investigate gene x gene interactions in human data. Copyright (c) 2007 S. Karger AG, Basel.
引用
收藏
页码:67 / 84
页数:18
相关论文
共 135 条
[1]   A mixture model approach for the analysis of microarray gene expression data [J].
Allison, DB ;
Gadbury, GL ;
Heo, MS ;
Fernández, JR ;
Lee, CK ;
Prolla, TA ;
Weindruch, R .
COMPUTATIONAL STATISTICS & DATA ANALYSIS, 2002, 39 (01) :1-20
[2]  
Anderson U, 1998, AUDITING-J PRACT TH, V17, P1
[3]   Concordance of multiple analytical approaches demonstrates a complex relationship between DNA repair gene SNPs, smoking and bladder cancer susceptibility [J].
Andrew, AS ;
Nelson, HH ;
Kelsey, KT ;
Moore, JH ;
Meng, AC ;
Casella, DP ;
Tosteson, TD ;
Schned, AR ;
Karagas, MR .
CARCINOGENESIS, 2006, 27 (05) :1030-1037
[4]  
[Anonymous], 2011, Categorical data analysis
[5]  
[Anonymous], PRINCIPLES DATA MINI
[6]   Oligogenic combinations associated with breast cancer risk in women under 53 years of age [J].
Aston, CE ;
Ralph, DA ;
Lalo, DP ;
Manjeshwar, S ;
Gramling, BA ;
DeFreese, DC ;
West, AD ;
Branam, DE ;
Thompson, LF ;
Craft, MA ;
Mitchell, DS ;
Shimasaki, CD ;
Mulvihill, JJ ;
Jupe, ER .
HUMAN GENETICS, 2005, 116 (03) :208-221
[7]   Dissection of epistasis in oligogenic Bardet-Biedl syndrome [J].
Badano, JL ;
Leitch, CC ;
Ansley, SJ ;
May-Simera, H ;
Lawson, S ;
Lewis, RA ;
Beales, PL ;
Dietz, HC ;
Fisher, S ;
Katsanis, N .
NATURE, 2006, 439 (7074) :326-330
[8]   Testing for gene-gene interaction controlling total IgE in families from Barbados: Evidence of sensitivity regarding linkage heterogeneity among families [J].
Barnes, KC ;
Mathias, RA ;
Nickel, R ;
Freidhoff, LR ;
Stockton, ML ;
Xue, XL ;
Naidu, RP ;
Levett, PN ;
Casolaro, V ;
Beaty, TH .
GENOMICS, 2001, 71 (02) :246-251
[9]  
Bateson W., 1909, Mendel's Principles of Heredity
[10]   Haplotype interaction analysis of unlinked regions [J].
Becker, T ;
Schumacher, J ;
Cichon, S ;
Baur, MP ;
Knapp, M .
GENETIC EPIDEMIOLOGY, 2005, 29 (04) :313-322