Adaptive SNP-Set Association Testing in Generalized Linear Mixed Models with Application to Family Studies

被引:8
作者
Park, Jun Young [1 ]
Wu, Chong [1 ]
Basu, Saonli [1 ]
McGue, Matt [2 ]
Pan, Wei [1 ]
机构
[1] Univ Minnesota, Div Biostat, A460 Mayo Bldg,MMC 303,420 Delaware St SE, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Dept Psychol, A460 Mayo Bldg,MMC 303,420 Delaware St SE, Minneapolis, MN 55455 USA
基金
美国国家卫生研究院;
关键词
Alcohol dependence; aSPU; GEE; GLMM; GWAS; Score test; MELANIN-CONCENTRATING HORMONE; GENOME-WIDE ASSOCIATION; GENETIC ASSOCIATION; BIAS CORRECTION; RARE VARIANTS; POWERFUL; TRAITS; COMPONENTS; DISPERSION; TWIN;
D O I
10.1007/s10519-017-9883-x
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
In genome-wide association studies (GWAS), it has been increasingly recognized that, as a complementary approach to standard single SNP analyses, it may be beneficial to analyze a group of functionally related SNPs together. Among the existent population-based SNP-set association tests, two adaptive tests, the aSPU test and the aSPUpath test, offer a powerful and general approach at the gene- and pathway-levels by data-adaptively combining the results across multiple SNPs (and genes) such that high statistical power can be maintained across a wide range of scenarios. We extend the aSPU and the aSPUpath test to familial data under the framework of the generalized linear mixed models (GLMMs), which can take account of both subject relatedness and possible population structure. As in population-based GWAS, the proposed aSPU and aSPUpath tests require only fitting a single and common GLMM (under the null hypothesis) for all the SNPs, thus are computationally efficient and feasible for large GWAS data. We illustrate our approaches in identifying genes and pathways associated with alcohol dependence in the Minnesota Twin Family Study. The aSPU test detected a gene associated with the trait, in contrast to none by the standard single SNP analysis. Our aSPU test also controlled Type I errors satisfactorily in a small simulation study. We provide R code to conduct the aSPU and aSPUpath tests for familial and other correlated data.
引用
收藏
页码:55 / 66
页数:12
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    Koh, Hyunwook
    Li, Yutong
    Zhan, Xiang
    Chen, Jun
    Zhao, Ni
    [J]. FRONTIERS IN GENETICS, 2019, 10
  • [32] Permutation-based variance component test in generalized linear mixed model with application to multilocus genetic association study
    Zeng, Ping
    Zhao, Yang
    Li, Hongliang
    Wang, Ting
    Chen, Feng
    [J]. BMC MEDICAL RESEARCH METHODOLOGY, 2015, 15 : 1 - 9
  • [33] BGWAS: Bayesian variable selection in linear mixed models with nonlocal priors for genome-wide association studies
    Williams, Jacob
    Xu, Shuangshuang
    Ferreira, Marco A. R.
    [J]. BMC BIOINFORMATICS, 2023, 24 (01)
  • [34] BGWAS: Bayesian variable selection in linear mixed models with nonlocal priors for genome-wide association studies
    Jacob Williams
    Shuangshuang Xu
    Marco A. R. Ferreira
    [J]. BMC Bioinformatics, 24
  • [35] Iterative hard thresholding in genome-wide association studies: Generalized linear models, prior weights, and double sparsity
    Chu, Benjamin B.
    Keys, Kevin L.
    German, Christopher A.
    Zhou, Hua
    Zhou, Jin J.
    Sobel, Eric M.
    Sinsheimer, Janet S.
    Lange, Kenneth
    [J]. GIGASCIENCE, 2020, 9 (06):
  • [36] Computationally efficient familywise error rate control in genome-wide association studies using score tests for generalized linear models
    Halle, Kari Krizak
    Bakke, Oyvind
    Djurovic, Srdjan
    Bye, Anja
    Ryeng, Einar
    Wisloff, Ulrik
    Andreassen, Ole A.
    Langaas, Mette
    [J]. SCANDINAVIAN JOURNAL OF STATISTICS, 2020, 47 (04) : 1090 - 1113
  • [37] High performance implementation of the hierarchical likelihood for generalized linear mixed models: an application to estimate the potassium reference range in massive electronic health records datasets
    Bologa, Cristian G.
    Pankratz, Vernon Shane
    Unruh, Mark L.
    Roumelioti, Maria Eleni
    Shah, Vallabh
    Shaffi, Saeed Kamran
    Arzhan, Soraya
    Cook, John
    Argyropoulos, Christos
    [J]. BMC MEDICAL RESEARCH METHODOLOGY, 2021, 21 (01)