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

Genetics. 2014 Apr;196(4):1293-302. doi: 10.1534/genetics.113.160739. Epub 2014 Feb 4.

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Algorithms
  • Computational Biology / methods*
  • Gene Frequency
  • Genetic Variation
  • Genome
  • Genome-Wide Association Study / methods*
  • Linkage Disequilibrium
  • Models, Genetic
  • Models, Statistical
  • Polymorphism, Single Nucleotide