Enhancing the Power to Detect Low-Frequency Variants in Genome-Wide Screens

Author:

Lin Chang-Yun12,Xing Guan3,Ku Hung-Chih1,Elston Robert C4,Xing Chao11

Affiliation:

1. McDermott Center of Human Growth and Development, University of Texas Southwestern Medical Center, Dallas, Texas 75390

2. Department of Applied Mathematics and Institute of Statistics, National Chung Hsing University, Taichung, Taiwan

3. Bristol-Myers Squibb Company, Pennington, New Jersey 08534

4. Department of Epidemiology and Biostatistics, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106

Abstract

Abstract In genetic association studies a conventional test statistic is proportional to the correlation coefficient between the trait and the variant, with the result that it lacks power to detect association for low-frequency variants. Considering the link between the conventional association test statistics and the linkage disequilibrium measure r2, we propose a test statistic analogous to the standardized linkage disequilibrium D′ to increase the power of detecting association for low-frequency variants. By both simulation and real data analysis we show that the proposed D′ test is more powerful than the conventional methods for detecting association for low-frequency variants in a genome-wide setting. The optimal coding strategy for the D′ test and its asymptotic properties are also investigated. In summary, we advocate using the D′ test in a dominant model as a complementary approach to enhancing the power of detecting association for low-frequency variants with moderate to large effect sizes in case-control genome-wide association studies.

Publisher

Oxford University Press (OUP)

Subject

Genetics

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