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Measuring Pharmacogene Variant Function at Scale Using Multiplexed Assays

  • ,
  • Gabriel Boyle
    ,
  • Clara J. Amorosi
    ,
  • Douglas M. Fowler
    ,
  • Maitreya J. Dunham
  • University of Washington
    ,
  • Department of Bioengineering
Research Output:
Contribution to journal
Review article
Peer-review

Open access

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.

Bibliographic Information

Output type

Research Output:
Contribution to journal
Review article
Peer-review

Original language

English

Pages from-to (Number of pages)

Pages 531-550 (20 pages)

Journal (Volume, Issue Number)

Annual Review of Pharmacology and Toxicology (Volume 62)

Publication milestones

  • Published - 06/01/2022

Publication status

Published - 06/01/2022

ISSN

0362-1642

Publication IDs

  • Scopus: 85123389734
  • PubMed: 34516287