Leveraging the HapMap correlation structure in association studies

被引:52
作者
Zaitlen, Noah
Kang, Hyun Min
Eskin, Eleazar
Halperin, Eran
机构
[1] Int Comp Sci Inst, Berkeley, CA 94704 USA
[2] Univ Calif San Diego, Bioinformat Program, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Dept Comp Sci & Engn, La Jolla, CA 92093 USA
[4] Univ Calif Los Angeles, Dept Comp Sci, Los Angeles, CA 90024 USA
[5] Univ Calif Los Angeles, Dept Human Genet, Los Angeles, CA 90024 USA
关键词
D O I
10.1086/513109
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Recent high-throughput genotyping technologies, such as the Affymetrix 500k array and the Illumina HumanHap 550 beadchip, have driven down the costs of association studies and have enabled the measurement of single-nucleotide polymorphism (SNP) allele frequency differences between case and control populations on a genomewide scale. A key aspect in the efficiency of association studies is the notion of "indirect association," where only a subset of SNPs are collected to serve as proxies for the uncollected SNPs, taking advantage of the correlation structure between SNPs. Recently, a new class of methods for indirect association, multimarker methods, has been proposed. Although the multimarker methods are a considerable advancement, current methods do not fully take advantage of the correlation structure between SNPs and their multimarker proxies. In this article, we propose a novel multimarker indirect-association method, WHAP, that is based on a weighted sum of the haplotype frequency differences. In contrast to traditional indirect-association methods, we show analytically that there is a considerable gain in power achieved by our method compared with both single-marker and multimarker tests, as well as traditional haplotype-based tests. Our results are supported by empirical evaluation across the HapMap reference panel data sets, and a software implementation for the Affymetrix 500k and Illumina HumanHap 550 chips is available for download.
引用
收藏
页码:683 / 691
页数:9
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