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POIROT: a powerful test for parent-of-origin effects in unrelated samples leveraging multiple phenotypes.
Head, S Taylor; Leslie, Elizabeth J; Cutler, David J; Epstein, Michael P.
Afiliação
  • Head ST; Department of Biostatistics and Bioinformatics, Rollins School of Public Health, Emory University, Atlanta, GA 30322, United States.
  • Leslie EJ; Department of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, United States.
  • Cutler DJ; Department of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, United States.
  • Epstein MP; Department of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, United States.
Bioinformatics ; 39(4)2023 04 03.
Article em En | MEDLINE | ID: mdl-37067493
MOTIVATION: There is widespread interest in identifying genetic variants that exhibit parent-of-origin effects (POEs) wherein the effect of an allele on phenotype expression depends on its parental origin. POEs can arise from different phenomena including genomic imprinting and have been documented for many complex traits. Traditional tests for POEs require family data to determine parental origins of transmitted alleles. As most genome-wide association studies (GWAS) sample unrelated individuals (where allelic parental origin is unknown), the study of POEs in such datasets requires sophisticated statistical methods that exploit genetic patterns we anticipate observing when POEs exist. We propose a method to improve discovery of POE variants in large-scale GWAS samples that leverages potential pleiotropy among multiple correlated traits often collected in such studies. Our method compares the phenotypic covariance matrix of heterozygotes to homozygotes based on a Robust Omnibus Test. We refer to our method as the Parent of Origin Inference using Robust Omnibus Test (POIROT) of multiple quantitative traits. RESULTS: Through simulation studies, we compared POIROT to a competing univariate variance-based method which considers separate analysis of each phenotype. We observed POIROT to be well-calibrated with improved power to detect POEs compared to univariate methods. POIROT is robust to non-normality of phenotypes and can adjust for population stratification and other confounders. Finally, we applied POIROT to GWAS data from the UK Biobank using BMI and two cholesterol phenotypes. We identified 338 genome-wide significant loci for follow-up investigation. AVAILABILITY AND IMPLEMENTATION: The code for this method is available at https://github.com/staylorhead/POIROT-POE.
Assuntos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Testes Genéticos / Estudo de Associação Genômica Ampla Tipo de estudo: Prognostic_studies Idioma: En Revista: Bioinformatics Assunto da revista: INFORMATICA MEDICA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Testes Genéticos / Estudo de Associação Genômica Ampla Tipo de estudo: Prognostic_studies Idioma: En Revista: Bioinformatics Assunto da revista: INFORMATICA MEDICA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos