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Ancestry deconvolution and partial polygenic score can improve susceptibility predictions in recently admixed individuals.
Marnetto, Davide; Pärna, Katri; Läll, Kristi; Molinaro, Ludovica; Montinaro, Francesco; Haller, Toomas; Metspalu, Mait; Mägi, Reedik; Fischer, Krista; Pagani, Luca.
Afiliação
  • Marnetto D; Institute of Genomics, University of Tartu, Riia 23b, 51010, Tartu, Estonia. davide.marnetto@ut.ee.
  • Pärna K; Institute of Genomics, University of Tartu, Riia 23b, 51010, Tartu, Estonia.
  • Läll K; Institute of Molecular and Cell Biology, University of Tartu, Riia 23, 51010, Tartu, Estonia.
  • Molinaro L; Department of Epidemiology, University Medical Center Groningen, Hanzeplein 1, 9713 GZ, Groningen, The Netherlands.
  • Montinaro F; Institute of Genomics, University of Tartu, Riia 23b, 51010, Tartu, Estonia.
  • Haller T; Institute of Genomics, University of Tartu, Riia 23b, 51010, Tartu, Estonia.
  • Metspalu M; Institute of Molecular and Cell Biology, University of Tartu, Riia 23, 51010, Tartu, Estonia.
  • Mägi R; Institute of Genomics, University of Tartu, Riia 23b, 51010, Tartu, Estonia.
  • Fischer K; Institute of Genomics, University of Tartu, Riia 23b, 51010, Tartu, Estonia.
  • Pagani L; Institute of Genomics, University of Tartu, Riia 23b, 51010, Tartu, Estonia.
Nat Commun ; 11(1): 1628, 2020 04 02.
Article em En | MEDLINE | ID: mdl-32242022
Polygenic Scores (PSs) describe the genetic component of an individual's quantitative phenotype or their susceptibility to diseases with a genetic basis. Currently, PSs rely on population-dependent contributions of many associated alleles, with limited applicability to understudied populations and recently admixed individuals. Here we introduce a combination of local ancestry deconvolution and partial PS computation to account for the population-specific nature of the association signals in individuals with admixed ancestry. We demonstrate partial PS to be a proxy for the total PS and that a portion of the genome is enough to improve susceptibility predictions for the traits we test. By combining partial PSs from different populations, we are able to improve trait predictability in admixed individuals with some European ancestry. These results may extend the applicability of PSs to subjects with a complex history of admixture, where current methods cannot be applied.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Herança Multifatorial Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estônia

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Herança Multifatorial Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estônia