Literature DB >> 24496013

Enhancing the power to detect low-frequency variants in genome-wide screens.

Chang-Yun Lin1, Guan Xing, Hung-Chih Ku, Robert C Elston, Chao Xing.   

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 r(2), 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.

Keywords:  case-control study; genome-wide screen; linkage disequilibrium; low-frequency variants

Mesh:

Year:  2014        PMID: 24496013      PMCID: PMC3982702          DOI: 10.1534/genetics.113.160739

Source DB:  PubMed          Journal:  Genetics        ISSN: 0016-6731            Impact factor:   4.562


  41 in total

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10.  Designing genome-wide association studies: sample size, power, imputation, and the choice of genotyping chip.

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