Optimal DNA Pooling-Based Two-Stage Designs in Case-Control Association Studies

被引:10
|
作者
Zhao, Yihong [1 ]
Wang, Shuang [1 ]
机构
[1] Columbia Univ, Mailman Sch Publ Hlth, Dept Biostat, New York, NY 10032 USA
关键词
Two-stage design; DNA-pooling; Genome-wide association study; Measurement errors; Optimal design; GENOME-WIDE ASSOCIATION; DISEASE; SNP; IDENTIFICATION; FUTURE;
D O I
10.1159/000164398
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Study cost remains the major limiting factor for genomewide association studies due to the necessity of genotyping a large number of SNPs for a large number of subjects. Both DNA pooling strategies and two-stage designs have been proposed to reduce genotyping costs. In this study, we propose a cost-effective, two-stage approach with a DNA pooling strategy. During stage I, all markers are evaluated on a subset of individuals using DNA pooling. The most promising set of markers is then evaluated with individual genotyping for all individuals during stage II. The goal is to determine the optimal parameters (pi(p)(sample), the proportion of samples used during stage I with DNA pooling; and pi(p)(marker), the proportion of markers evaluated during stage II with individual genotyping) that minimize the cost of a two-stage DNA pooling design while maintaining a desired overall significance level and achieving a level of power similar to that of a one-stage individual genotyping design. We considered the effects of three factors on optimal two-stage DNA pooling designs. Our results suggest that, under most scenarios considered, the optimal two-stage DNA pooling design may be much more cost-effective than the optimal two-stage individual genotyping design, which use individual genotyping during both stages. Copyright (C) 2008 S. Karger AG, Basel
引用
收藏
页码:46 / 56
页数:11
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