Document Type

Article

Version Deposited

Published Version

Publication Date

3-12-2024

Publication Title

Frontiers in Bioinformatics

DOI

10.3389/fbinf.2024.1351620

Abstract

Long-read sequencing technologies offer new opportunities to generate high-confidence phased whole-genome sequencing data for robust pharmacogenetic annotation. Here, we describe a new user-friendly R package, ursaPGx, designed to accept multi-sample phased whole-genome sequencing data VCF input files and output star allele annotations for pharmacogenes annotated in PharmVar.

Comments

© 2024 Calendo, Kusic, Madzo, Gharani and Scheinfeldt. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY).

Creative Commons License

Creative Commons Attribution 4.0 International License
This work is licensed under a Creative Commons Attribution 4.0 International License.

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