Literature DB >> 34516287

Measuring Pharmacogene Variant Function at Scale Using Multiplexed Assays.

Renee C Geck1, Gabriel Boyle1, Clara J Amorosi1, Douglas M Fowler1,2, Maitreya J Dunham1.   

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.

Entities:  

Keywords:  deep mutational scan; multiplexed assay of variant effect; next-generation sequencing; pharmacogenomics; precision medicine; variable drug response

Mesh:

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Year:  2021        PMID: 34516287     DOI: 10.1146/annurev-pharmtox-032221-085807

Source DB:  PubMed          Journal:  Annu Rev Pharmacol Toxicol        ISSN: 0362-1642            Impact factor:   13.820


  1 in total

Review 1.  Keeping pace with CYP2D6 haplotype discovery: innovative methods to assign function.

Authors:  Karen E Brown; Jack W Staples; Erica L Woodahl
Journal:  Pharmacogenomics       Date:  2022-01-27       Impact factor: 2.533

  1 in total

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