Ferreira Teresa, Marchini Jonathan
Department of Statistics, University of Oxford, UK.
Ann Hum Genet. 2011 Jan;75(1):1-9. doi: 10.1111/j.1469-1809.2010.00618.x. Epub 2010 Nov 30.
Genome-wide association studies (GWAS) are now clearly established as a powerful method for detecting loci involved in the etiology of common complex diseases. Most diseases and traits studied using the GWAS approach now have several loci that have been shown to be convincingly replicated. It is generally the case that these loci have been identified using single locus association scans of genotyped or imputed SNPs and very few loci have been identified by taking interactions into account. We propose a method that assesses the evidence of association at each SNP by modeling the effect of the locus in combination with other known loci. We use a Bayesian model averaging approach that combines the evidence across several different plausible models for the way in which the loci interact. We show that the method has good power both when the association is the result of marginal effects only, and when interaction with a known locus occurs. The method is implemented as an option in the program SNPTEST.
全基因组关联研究(GWAS)现已明确成为检测与常见复杂疾病病因相关基因座的有力方法。目前,使用GWAS方法研究的大多数疾病和性状都有几个已被证实可重复的基因座。通常情况下,这些基因座是通过对基因分型或推算的单核苷酸多态性(SNP)进行单基因座关联扫描来确定的,很少有基因座是通过考虑相互作用来确定的。我们提出了一种方法,通过对该基因座与其他已知基因座的联合效应进行建模,来评估每个SNP的关联证据。我们使用贝叶斯模型平均方法,该方法结合了多个不同的合理模型中基因座相互作用方式的证据。我们表明,该方法在关联仅由边际效应导致时以及与已知基因座发生相互作用时都具有良好的功效。该方法作为程序SNPTEST中的一个选项来实现。