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Linear mixed models for association analysis of quantitative traits with next-generation sequencing data.
Chiu, Chi-Yang; Yuan, Fang; Zhang, Bing-Song; Yuan, Ao; Li, Xin; Fang, Hong-Bin; Lange, Kenneth; Weeks, Daniel E; Wilson, Alexander F; Bailey-Wilson, Joan E; Musolf, Anthony M; Stambolian, Dwight; Lakhal-Chaieb, M'Hamed Lajmi; Cook, Richard J; McMahon, Francis J; Amos, Christopher I; Xiong, Momiao; Fan, Ruzong.
  • Chiu CY; Division of Biostatistics, Department of Preventive Medicine, University of Tennessee Health Science Center, Memphis, Tennessee.
  • Yuan F; Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health (NIH), Bethesda, Maryland.
  • Zhang BS; Department of Biochemistry and Molecular Biology, School of Basic Medicine, Kunming Medical University, Kunming, Yunnan, China.
  • Yuan A; Department of Biostatistics, Bioinformatics, and Biomathematics, Georgetown University Medical Center, Washington, District of Columbia.
  • Li X; Department of Biostatistics, Bioinformatics, and Biomathematics, Georgetown University Medical Center, Washington, District of Columbia.
  • Fang HB; Department of Biostatistics, Bioinformatics, and Biomathematics, Georgetown University Medical Center, Washington, District of Columbia.
  • Lange K; Department of Biostatistics, Bioinformatics, and Biomathematics, Georgetown University Medical Center, Washington, District of Columbia.
  • Weeks DE; Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, California.
  • Wilson AF; Department of Biostatistics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Bailey-Wilson JE; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Musolf AM; Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health (NIH), Bethesda, Maryland.
  • Stambolian D; Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health (NIH), Bethesda, Maryland.
  • Lakhal-Chaieb ML; Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health (NIH), Bethesda, Maryland.
  • Cook RJ; Department of Genetics, University of Pennsylvania, Philadelphia, Pennsylvania.
  • McMahon FJ; Department de Mathematiques et de Statistique, Universite Laval, Quebec, Canada.
  • Amos CI; Department of Statistics and Actuarial Science, Waterloo, Ontario, Quebec, Canada.
  • Xiong M; Human Genetics Branch and Genetic Basis of Mood and Anxiety Disorders Section, University of Waterloo, National Institute of Mental Health, NIH, Bethesda, Maryland.
  • Fan R; Department of Medicine, Baylor College of Medicine, Houston, Texas.
Genet Epidemiol ; 43(2): 189-206, 2019 Mar.
Article en En | MEDLINE | ID: mdl-30537345
ABSTRACT
We develop linear mixed models (LMMs) and functional linear mixed models (FLMMs) for gene-based tests of association between a quantitative trait and genetic variants on pedigrees. The effects of a major gene are modeled as a fixed effect, the contributions of polygenes are modeled as a random effect, and the correlations of pedigree members are modeled via inbreeding/kinship coefficients. F -statistics and χ 2 likelihood ratio test (LRT) statistics based on the LMMs and FLMMs are constructed to test for association. We show empirically that the F -distributed statistics provide a good control of the type I error rate. The F -test statistics of the LMMs have similar or higher power than the FLMMs, kernel-based famSKAT (family-based sequence kernel association test), and burden test famBT (family-based burden test). The F -statistics of the FLMMs perform well when analyzing a combination of rare and common variants. For small samples, the LRT statistics of the FLMMs control the type I error rate well at the nominal levels α = 0.01 and 0.05 . For moderate/large samples, the LRT statistics of the FLMMs control the type I error rates well. The LRT statistics of the LMMs can lead to inflated type I error rates. The proposed models are useful in whole genome and whole exome association studies of complex traits.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Carácter Cuantitativo Heredable / Estudios de Asociación Genética / Secuenciación de Nucleótidos de Alto Rendimiento / Modelos Genéticos Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Año: 2019 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Carácter Cuantitativo Heredable / Estudios de Asociación Genética / Secuenciación de Nucleótidos de Alto Rendimiento / Modelos Genéticos Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Año: 2019 Tipo del documento: Article