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Identifying latent genetic interactions in genome-wide association studies using multiple traits.
Bass, Andrew J; Bian, Shijia; Wingo, Aliza P; Wingo, Thomas S; Cutler, David J; Epstein, Michael P.
Afiliação
  • Bass AJ; Department of Human Genetics, Emory University, Atlanta, GA, 30322, USA. ajbass@emory.edu.
  • Bian S; Department of Biostatistics and Bioinformatics, Emory University, Atlanta, GA, 30322, USA.
  • Wingo AP; Department of Psychiatry, Emory University, Atlanta, GA, 30322, USA.
  • Wingo TS; Department of Human Genetics, Emory University, Atlanta, GA, 30322, USA.
  • Cutler DJ; Department of Neurology, Emory University, Atlanta, GA, 30322, USA.
  • Epstein MP; Department of Human Genetics, Emory University, Atlanta, GA, 30322, USA.
Genome Med ; 16(1): 62, 2024 04 25.
Article em En | MEDLINE | ID: mdl-38664839
ABSTRACT
The "missing" heritability of complex traits may be partly explained by genetic variants interacting with other genes or environments that are difficult to specify, observe, and detect. We propose a new kernel-based method called Latent Interaction Testing (LIT) to screen for genetic interactions that leverages pleiotropy from multiple related traits without requiring the interacting variable to be specified or observed. Using simulated data, we demonstrate that LIT increases power to detect latent genetic interactions compared to univariate methods. We then apply LIT to obesity-related traits in the UK Biobank and detect variants with interactive effects near known obesity-related genes (URL https//CRAN.R-project.org/package=lit ).
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Estudo de Associação Genômica Ampla / Obesidade Limite: Humans Idioma: En Revista: Genome Med Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Estudo de Associação Genômica Ampla / Obesidade Limite: Humans Idioma: En Revista: Genome Med Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Reino Unido