You've Gotta Be Lucky: Coverage and the Elusive Gene–Gene Interaction

Genome‐wide association studies (GWAS) have led to a large number of single‐SNP association findings, but there has been, so far, no investigation resulting in the discovery of a replicable gene–gene interaction. In this paper, we examine some of the possible explanations for the lack of findings, and argue that coverage of causal variation not only has a large effect on the loss in power, but that the effect is larger than in the single‐SNP analyses. We show that the product of linkage disequilibrium measures, r2, between causal and tested SNPs offers a good approximation to the loss in efficiency as defined by the ratio of sample sizes that lead to similar power. We also demonstrate that, in addition to the huge search space, the loss in power due to coverage when using commercially available platforms makes the search for gene–gene interactions daunting.

[1]  Judy H. Cho,et al.  Finding the missing heritability of complex diseases , 2009, Nature.

[2]  Xiaoquan Wen,et al.  Coverage and Characteristics of the Affymetrix GeneChip Human Mapping 100K SNP Set , 2006, PLoS genetics.

[3]  Pauline C Ng,et al.  Power to Detect Risk Alleles Using Genome-Wide Tag SNP Panels , 2007, PLoS genetics.

[4]  M. Rieder,et al.  Estimating coverage and power for genetic association studies using near-complete variation data , 2008, Nature Genetics.

[5]  K. Mossman The Wellcome Trust Case Control Consortium, U.K. , 2008 .

[6]  M. Olivier A haplotype map of the human genome , 2003, Nature.

[7]  P. Donnelly,et al.  Genome-wide strategies for detecting multiple loci that influence complex diseases , 2005, Nature Genetics.

[8]  N. Cox,et al.  Trait-Associated SNPs Are More Likely to Be eQTLs: Annotation to Enhance Discovery from GWAS , 2010, PLoS genetics.

[9]  L. Kruglyak Prospects for whole-genome linkage disequilibrium mapping of common disease genes , 1999, Nature Genetics.

[10]  M. Olivier A haplotype map of the human genome. , 2003, Nature.

[11]  Lon R Cardon,et al.  Evaluating coverage of genome-wide association studies , 2006, Nature Genetics.

[12]  Simon C. Potter,et al.  Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls , 2007, Nature.

[13]  Wei Zhang,et al.  SCAN: SNP and copy number annotation , 2010, Bioinform..

[14]  H. Cordell Detecting gene–gene interactions that underlie human diseases , 2009, Nature Reviews Genetics.

[15]  Dan L Nicolae,et al.  Quantifying the amount of missing information in genetic association studies , 2006, Genetic epidemiology.

[16]  H. Cordell Epistasis: what it means, what it doesn't mean, and statistical methods to detect it in humans. , 2002, Human molecular genetics.

[17]  J. Pritchard,et al.  Linkage disequilibrium in humans: models and data. , 2001, American journal of human genetics.