Abstract

As a pivotal research tool, genome-wide association study has successfully identified numerous genetic variants underlying distinct diseases. However, these identified genetic variants only explain a small proportion of the phenotypic variation for certain diseases, suggesting that there are still more genetic signals to be detected. One of the reasons may be that one-phenotype one-variant association study is not so efficient in detecting variants of weak effects. Nowadays, it is increasingly worth noting that joint analysis of multiple phenotypes may boost the statistical power to detect pathogenic variants with weak genetic effects on complex diseases, providing more clues for their underlying biology mechanisms. So a Weighted Combination of multiple phenotypes following Hierarchical Clustering method (WCHC) is proposed for simultaneously analyzing multiple phenotypes in association studies. A series of simulations are conducted, and the results show that WCHC is either the most powerful method or comparable with the most powerful competitor in most of the simulation scenarios. Additionally, we evaluated the performance of WCHC in its application to the obesity-related phenotypes from Atherosclerosis Risk in Communities, and several associated variants are reported.

Highlights

  • Genome-Wide Association Studies studies (GWASs) aim to identify genetic variants associated with certain phenotypes for explaining complex diseases (O’Reilly et al, 2012; Yang and Wang, 2012)

  • The p-values of WCHC, Weighted Combination of multiple Phenotypes (WCmulP), and SHet are evaluated by 2,000 permutations; and the p-values of MANOVA, MultiPhen, TATES, and OB are evaluated by their asymptotic distributions

  • It is observed from these two tables that most of the type I error rates of WCHC are within 95% confidence intervals (CIs), which shows the validity of the developed WCHC

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Summary

Introduction

Genome-Wide Association Studies studies (GWASs) aim to identify genetic variants associated with certain phenotypes for explaining complex diseases (O’Reilly et al, 2012; Yang and Wang, 2012). Jointly analyzing multiple phenotypes can enhance the power of association tests to identify genetic markers associated with one or more phenotypes (Aschard et al, 2014). One of the common approaches for analyzing multiple related phenotypes is to conduct singlephenotype separately and report the results for each phenotype (O’Reilly et al, 2012). Joint analysis of multiple phenotypes has become catching on because of its enhanced statistical power in the detection of genetic variants compared to analysis for each phenotype separately (Yang Q. et al, 2010; Aschard et al, 2014)

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