Abstract

The choice of a statistical method significantly affects the power profiles of Genome Wide Association (GWA) predictions. Previous simulation studies of a single synthetic phenotype marker determined that the gene model or mode of inheritance (MOI) was a major influence on power. In this paper, the authors compare the power profiles of GWA statistical methods that combine MOI specific methods into multiple test scenarios against individual methods that may or not assume a MOI gene model consistent with the marker that predicts the association. Combining recessive, additive and dominant individual tests, and using either the Bonferroni Correction method or the MAX test (Li et al., 2008) has power implications with respect to single test GWA-based methods. If the gene model behind the associated phenotype is not known, a multiple test procedure could have significant advantages with respect to single test procedures. Our findings do not provide a specific answer as to which statistical method is best. The best method depends on the MOI gene model associated with the phenotype (diagnosis) in question. However, our results do indicate that the common assumption that the MOI of the locus associated with the diagnosis is additive has consequences. Our results indicate that researchers should consider a multi-test procedure that combines the results of individual MOI-based core tests as a statistical method for conducting the initial screen in a GW study. The process for combining the core tests into a single operational test can occur in a number of ways. We identify two: the Bonferroni procedures and the MAX procedure, each of which produce very similar statistical power profiles.

Highlights

  • In this study, we examine statistical methods used to perform genome wide association studies (GWAS)

  • Our goal is to identify marker properties that can be linked to optimal methods for predicting associations in GWAS

  • The additive χ2 version of the CA (CA-A) test, which was the best method for both additive and multiplicative gene models but not effective when applied to recessive mode of inheritance (MOI) data

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Summary

Introduction

We examine statistical methods used to perform genome wide association studies (GWAS). GWAS usually apply univariate statistical tests to each gene marker or single nucleotide polymorphism (SNP) as an initial step. This SNP based test is statistically straightforward and the testing is done with standard methods (e.g. χ2 tests, regression) that have been studied outside of the GWAS context. The literature contains a number of papers that make statistical power comparisons among subsets of these methods, including Sasieni (1997) and Freidlin et al (2002), but the question of which method is best suited to univariate scanning in a GWAS remains an open issue. The choice of method depends on the match between the true genetic model underpinning the association and the type of model assumed by the method

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