Your browser doesn't support javascript.
loading
Genotype imputation and polygenic score estimation in northwestern Russian population.
Kolosov, Nikita; Rezapova, Valeriia; Rotar, Oxana; Loboda, Alexander; Freylikhman, Olga; Melnik, Olesya; Sergushichev, Alexey; Stevens, Christine; Voortman, Trudy; Kostareva, Anna; Konradi, Alexandra; Daly, Mark J; Artomov, Mykyta.
Afiliação
  • Kolosov N; Almazov National Medical Research Centre, Saint-Petersburg, Russia.
  • Rezapova V; ITMO University, Saint-Petersburg, Russia.
  • Rotar O; Broad Institute, Cambridge, MA, United States of America.
  • Loboda A; Almazov National Medical Research Centre, Saint-Petersburg, Russia.
  • Freylikhman O; ITMO University, Saint-Petersburg, Russia.
  • Melnik O; Broad Institute, Cambridge, MA, United States of America.
  • Sergushichev A; Almazov National Medical Research Centre, Saint-Petersburg, Russia.
  • Stevens C; Erasmus MC, University Medical Center, Rotterdam, The Netherlands.
  • Voortman T; Almazov National Medical Research Centre, Saint-Petersburg, Russia.
  • Kostareva A; ITMO University, Saint-Petersburg, Russia.
  • Konradi A; Broad Institute, Cambridge, MA, United States of America.
  • Daly MJ; Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA, United States of America.
  • Artomov M; Almazov National Medical Research Centre, Saint-Petersburg, Russia.
PLoS One ; 17(6): e0269434, 2022.
Article em En | MEDLINE | ID: mdl-35763490
ABSTRACT
Numerous studies demonstrated the lack of transferability of polygenic score (PGS) models across populations and the problem arising from unequal presentation of ancestries across genetic studies. However, even within European ancestry there are ethnic groups that are rarely presented in genetic studies. For instance, Russians, being one of the largest, diverse, and yet understudied group in Europe. In this study, we evaluated the reliability of genotype imputation for the Russian cohort by testing several commonly used imputation reference panels (e.g. HRC, 1000G, HGDP). HRC, in comparison with two other panels, showed the most accurate results based on both imputation accuracy and allele frequency concordance between masked and imputed genotypes. We built polygenic score models based on GWAS results from the UK biobank, measured the explained phenotypic variance in the Russian cohort attributed to polygenic scores for 11 phenotypes, collected in the clinic for each participant, and finally explored the role of allele frequency discordance between the UK biobank and the study cohort in the resulting PGS performance.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Herança Multifatorial / Polimorfismo de Nucleotídeo Único Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Herança Multifatorial / Polimorfismo de Nucleotídeo Único Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article