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Improving genetic risk prediction across diverse population by disentangling ancestry representations.
Gyawali, Prashnna K; Le Guen, Yann; Liu, Xiaoxia; Belloy, Michael E; Tang, Hua; Zou, James; He, Zihuai.
Afiliação
  • Gyawali PK; Department of Neurology and Neurological Sciences, Stanford University, Stanford, CA, USA. pgyawali@stanford.edu.
  • Le Guen Y; Department of Neurology and Neurological Sciences, Stanford University, Stanford, CA, USA.
  • Liu X; Institut du Cerveau-Paris Brain Institute-ICM, Paris, France.
  • Belloy ME; Department of Neurology and Neurological Sciences, Stanford University, Stanford, CA, USA.
  • Tang H; Department of Neurology and Neurological Sciences, Stanford University, Stanford, CA, USA.
  • Zou J; Department of Genetics, Stanford University, Stanford, CA, USA.
  • He Z; Department of Biomedical Data Science, Stanford University, Stanford, CA, USA. jamesz@stanford.edu.
Commun Biol ; 6(1): 964, 2023 09 22.
Article em En | MEDLINE | ID: mdl-37736834
ABSTRACT
Risk prediction models using genetic data have seen increasing traction in genomics. However, most of the polygenic risk models were developed using data from participants with similar (mostly European) ancestry. This can lead to biases in the risk predictors resulting in poor generalization when applied to minority populations and admixed individuals such as African Americans. To address this issue, largely due to the prediction models being biased by the underlying population structure, we propose a deep-learning framework that leverages data from diverse population and disentangles ancestry from the phenotype-relevant information in its representation. The ancestry disentangled representation can be used to build risk predictors that perform better across minority populations. We applied the proposed method to the analysis of Alzheimer's disease genetics. Comparing with standard linear and nonlinear risk prediction methods, the proposed method substantially improves risk prediction in minority populations, including admixed individuals, without needing self-reported ancestry information.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Medição de Risco / Predisposição Genética para Doença / Doença de Alzheimer Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Commun Biol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: ENGLAND / ESCOCIA / GB / GREAT BRITAIN / INGLATERRA / REINO UNIDO / SCOTLAND / UK / UNITED KINGDOM

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Medição de Risco / Predisposição Genética para Doença / Doença de Alzheimer Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Commun Biol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: ENGLAND / ESCOCIA / GB / GREAT BRITAIN / INGLATERRA / REINO UNIDO / SCOTLAND / UK / UNITED KINGDOM