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
相关论文
共 50 条
  • [41] Optimal two-stage reliability studies
    Browne, Ryan
    Steiner, Stefan H.
    MacKay, R. Jock
    STATISTICS IN MEDICINE, 2010, 29 (02) : 229 - 235
  • [42] A Novel Two-Stage Approach for Epistasis Detection in Genome-Wide Case-Control Studies
    Liao, Zhongli
    Zeng, Qingguang
    Liao, Bo
    Li, Xiong
    BIOCHEMICAL GENETICS, 2014, 52 (9-10) : 403 - 414
  • [43] Two-stage case-control studies: Precision of parameter estimates and considerations in selecting sample size
    Hanley, JA
    Csizmadi, I
    Collet, JP
    AMERICAN JOURNAL OF EPIDEMIOLOGY, 2005, 162 (12) : 1225 - 1234
  • [44] Optimal designs of two-stage studies for estimation of sensitivity, specificity and positive predictive value
    McNamee, R
    STATISTICS IN MEDICINE, 2002, 21 (23) : 3609 - 3625
  • [45] Optimal two-stage testing for family-based genome-wide association studies
    Macgregor, Stuart
    AMERICAN JOURNAL OF HUMAN GENETICS, 2008, 82 (03) : 797 - 799
  • [46] Two-stage designs for gene-disease association studies with sample size constraints
    Satagopan, JM
    Venkatraman, ES
    Begg, CB
    BIOMETRICS, 2004, 60 (03) : 589 - 597
  • [47] Leukocyte Mitochondrial DNA Copy Number and Risk of Thyroid Cancer: A Two-Stage Case-Control Study
    Zheng, Jian
    Cui, Ning-hua
    Zhang, Shuai
    Wang, Xue-bin
    Ming, Liang
    FRONTIERS IN ENDOCRINOLOGY, 2019, 10
  • [48] Determinants of the Incidence of Childhood Asthma: A Two-Stage Case-Control Study
    Martel, Marie-Josee
    Rey, Evelyne
    Malo, Jean-Luc
    Perreault, Sylvie
    Beauchesne, Marie-France
    Forget, Amelie
    Blais, Lucie
    AMERICAN JOURNAL OF EPIDEMIOLOGY, 2009, 169 (02) : 195 - 205
  • [49] Practical considerations for optimal two-stage designs with binary outcomes
    Ho, SY
    Yao, RJ
    AMERICAN STATISTICAL ASSOCIATION - 1996 PROCEEDINGS OF THE BIOPHARMACEUTICAL SECTION, 1996, : 108 - 111
  • [50] Optimal sample size division in two-stage seamless designs
    Berry, Lindsay R.
    Marion, Joe
    Berry, Scott M.
    Viele, Kert
    PHARMACEUTICAL STATISTICS, 2024, 23 (06) : 854 - 863