Your browser doesn't support javascript.
loading
Graphical analysis for phenome-wide causal discovery in genotyped population-scale biobanks.
Amar, David; Sinnott-Armstrong, Nasa; Ashley, Euan A; Rivas, Manuel A.
Afiliação
  • Amar D; Center for Inherited Cardiovascular Disease, Stanford University, Stanford, CA, USA.
  • Sinnott-Armstrong N; Department of Biomedical Data Science, Stanford University, Stanford, CA, USA.
  • Ashley EA; Department of Genetics, School of Medicine, Stanford University, Stanford, CA, USA.
  • Rivas MA; Center for Inherited Cardiovascular Disease, Stanford University, Stanford, CA, USA.
Nat Commun ; 12(1): 350, 2021 01 13.
Article em En | MEDLINE | ID: mdl-33441555
Causal inference via Mendelian randomization requires making strong assumptions about horizontal pleiotropy, where genetic instruments are connected to the outcome not only through the exposure. Here, we present causal Graphical Analysis Using Genetics (cGAUGE), a pipeline that overcomes these limitations using instrument filters with provable properties. This is achievable by identifying conditional independencies while examining multiple traits. cGAUGE also uses ExSep (Exposure-based Separation), a novel test for the existence of causal pathways that does not require selecting instruments. In simulated data we illustrate how cGAUGE can reduce the empirical false discovery rate by up to 30%, while retaining the majority of true discoveries. On 96 complex traits from 337,198 subjects from the UK Biobank, our results cover expected causal links and many new ones that were previously suggested by correlation-based observational studies. Notably, we identify multiple risk factors for cardiovascular disease, including red blood cell distribution width.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Bancos de Espécimes Biológicos / Herança Multifatorial / Estudo de Associação Genômica Ampla / Pleiotropia Genética Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Bancos de Espécimes Biológicos / Herança Multifatorial / Estudo de Associação Genômica Ampla / Pleiotropia Genética Idioma: En Ano de publicação: 2021 Tipo de documento: Article