Two-stage association tests for genome-wide association studies based on family data with arbitrary family structure

被引:0
|
作者
Tao Feng
Shuanglin Zhang
Qiuying Sha
机构
[1] Michigan Technological University,Department of Mathematical Sciences
[2] Heilongjiang University,Department of Mathematics
来源
关键词
two-stage design; genome-wide association study; family-based association test;
D O I
暂无
中图分类号
学科分类号
摘要
Recently, Steen et al proposed a two-stage approach for genome-wide family-based association studies. In the first stage, a screening test is used to select markers, and in the second stage, a family-based association test is performed on a much smaller set of the selected markers. The two-stage method can be much more powerful than the traditional family-based association tests. In this article, we extend the approach so that it can incorporate parental information and can be applied to an arbitrary pedigree structure. We use simulation studies to evaluate the type I error rates and the power of the proposed methods. Our results show that the two-stage approach that incorporates founders' phenotypes has the correct type I error rates, and is much more powerful than the two-stage approach that uses children's phenotypes only. Also, by carefully choosing the number of markers retained in the first stage, the power of a two-stage approach can be much more than that of the corresponding one-stage approach.
引用
收藏
页码:1169 / 1175
页数:6
相关论文
共 50 条
  • [31] Comparison of Methods to Account for Relatedness in Genome-Wide Association Studies with Family-Based Data
    Eu-ahsunthornwattana, Jakris
    Miller, E. Nancy
    Fakiola, Michaela
    Jeronimo, Selma M. B.
    Blackwell, Jenefer M.
    Cordell, Heather J.
    PLOS GENETICS, 2014, 10 (07):
  • [32] A data-driven weighting scheme for family-based genome-wide association studies
    Huaizhen Qin
    Tao Feng
    Shuanglin Zhang
    Qiuying Sha
    European Journal of Human Genetics, 2010, 18 : 596 - 603
  • [33] Robust Joint Analysis with Data Fusion in Two-Stage Quantitative Trait Genome-Wide Association Studies
    Pan, Dong-Dong
    Xiong, Wen-Jun
    Zhou, Ji-Yuan
    Pan, Ying
    Zhou, Guo-Li
    Fung, Wing-Kam
    COMPUTATIONAL AND MATHEMATICAL METHODS IN MEDICINE, 2013, 2013
  • [34] Genome-Wide Association Studies: Implications for Family Disease Risks
    Schaid, Daniel J.
    GENETIC EPIDEMIOLOGY, 2008, 32 (07) : 713 - 713
  • [35] Are linkage analysis and the collection of family data dead? Prospects for family studies in the age of genome-wide association
    Clerget-Darpoux, Francoise
    Elston, Robert C.
    HUMAN HEREDITY, 2007, 64 (02) : 91 - 96
  • [36] Joint Analysis for Genome-Wide Association Studies in Family-Based Designs
    Sha, Qiuying
    Zhang, Zhaogong
    Zhang, Shuanglin
    PLOS ONE, 2011, 6 (07):
  • [37] TWO-STAGE GENOME-WIDE ASSOCIATION STUDIES WITH DNA POOLING AND GENETIC MODEL SELECTION
    Yuan, Min
    Yang, Yaning
    Zheng, Gang
    STATISTICA SINICA, 2009, 19 (04) : 1769 - 1786
  • [38] Family-based studies to the rescue of genome-wide association studies in renal function
    Pattaro, Cristian
    Saint-Pierre, Aude
    KIDNEY INTERNATIONAL, 2013, 83 (02) : 196 - 198
  • [39] Genome-wide association tests by two-stage approaches with unified analysis of families and unrelated individuals
    Xuexia Wang
    Zhaogong Zhang
    Shuanglin Zhang
    Qiuying Sha
    BMC Proceedings, 1 (Suppl 1)
  • [40] On the Analysis of Genome-Wide Association Studies in Family-Based Designs: A Universal, Robust Analysis Approach and an Application to Four Genome-Wide Association Studies
    Won, Sungho
    Wilk, Jemma B.
    Mathias, Rasika A.
    O'Donnell, Christopher J.
    Silverman, Edwin K.
    Barnes, Kathleen
    O'Connor, George T.
    Weiss, Scott T.
    Lange, Christoph
    PLOS GENETICS, 2009, 5 (11)