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Estimating the effective sample size in association studies of quantitative traits.
Ziyatdinov, Andrey; Kim, Jihye; Prokopenko, Dmitry; Privé, Florian; Laporte, Fabien; Loh, Po-Ru; Kraft, Peter; Aschard, Hugues.
Affiliation
  • Ziyatdinov A; Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA 02115, USA.
  • Kim J; Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA 02115, USA.
  • Prokopenko D; Genetics and Aging Unit and McCance Center for Brain Health, Department of Neurology, Massachusetts General Hospital, Boston, MA 02114, USA.
  • Privé F; Harvard Medical School, Boston, MA 02115, USA.
  • Laporte F; National Centre for Register-Based Research, Aarhus University, Aarhus 8210, Denmark.
  • Loh PR; Department of Computational Biology-USR 3756 CNRS, Institut Pasteur, Paris 75015, France.
  • Kraft P; Division of Genetics, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115, USA.
  • Aschard H; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
G3 (Bethesda) ; 11(6)2021 06 17.
Article in En | MEDLINE | ID: mdl-33734375
The effective sample size (ESS) is a metric used to summarize in a single term the amount of correlation in a sample. It is of particular interest when predicting the statistical power of genome-wide association studies (GWAS) based on linear mixed models. Here, we introduce an analytical form of the ESS for mixed-model GWAS of quantitative traits and relate it to empirical estimators recently proposed. Using our framework, we derived approximations of the ESS for analyses of related and unrelated samples and for both marginal genetic and gene-environment interaction tests. We conducted simulations to validate our approximations and to provide a quantitative perspective on the statistical power of various scenarios, including power loss due to family relatedness and power gains due to conditioning on the polygenic signal. Our analyses also demonstrate that the power of gene-environment interaction GWAS in related individuals strongly depends on the family structure and exposure distribution. Finally, we performed a series of mixed-model GWAS on data from the UK Biobank and confirmed the simulation results. We notably found that the expected power drop due to family relatedness in the UK Biobank is negligible.
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Full text: 1 Database: MEDLINE Main subject: Multifactorial Inheritance / Genome-Wide Association Study Type of study: Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: G3 (Bethesda) Year: 2021 Type: Article Affiliation country: United States

Full text: 1 Database: MEDLINE Main subject: Multifactorial Inheritance / Genome-Wide Association Study Type of study: Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: G3 (Bethesda) Year: 2021 Type: Article Affiliation country: United States