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Measuring Pharmacogene Variant Function at Scale Using Multiplexed Assays.
Geck, Renee C; Boyle, Gabriel; Amorosi, Clara J; Fowler, Douglas M; Dunham, Maitreya J.
Afiliação
  • Geck RC; Department of Genome Sciences, University of Washington, Seattle, Washington 98195, USA; email: dfowler@uw.edu, maitreya@uw.edu.
  • Boyle G; Department of Genome Sciences, University of Washington, Seattle, Washington 98195, USA; email: dfowler@uw.edu, maitreya@uw.edu.
  • Amorosi CJ; Department of Genome Sciences, University of Washington, Seattle, Washington 98195, USA; email: dfowler@uw.edu, maitreya@uw.edu.
  • Fowler DM; Department of Genome Sciences, University of Washington, Seattle, Washington 98195, USA; email: dfowler@uw.edu, maitreya@uw.edu.
  • Dunham MJ; Department of Bioengineering, University of Washington, Seattle, Washington 98195, USA.
Annu Rev Pharmacol Toxicol ; 62: 531-550, 2022 01 06.
Article em En | MEDLINE | ID: mdl-34516287
ABSTRACT
As costs of next-generation sequencing decrease, identification of genetic variants has far outpaced our ability to understand their functional consequences. This lack of understanding is a central challenge to a key promise of pharmacogenomics using genetic information to guide drug selection and dosing. Recently developed multiplexed assays of variant effect enable experimental measurement of the function of thousands of variants simultaneously. Here, we describe multiplexed assays that have been performed on nearly 25,000 variants in eight key pharmacogenes (ADRB2, CYP2C9, CYP2C19, NUDT15, SLCO1B1, TMPT, VKORC1, and the LDLR promoter), discuss advances in experimental design, and explore key challenges that must be overcome to maximize the utility of multiplexed functional data.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Farmacogenética / Medicina de Precisão 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: Farmacogenética / Medicina de Precisão Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article