Development and validation of a pharmacogenomics reporting workflow based on the illumina global screening array chip

Background: Microarrays are a well-established and widely adopted technology capable of interrogating hundreds of thousands of loci across the human genome. Combined with imputation to cover common variants not included in the chip design, they offer a cost-effective solution for large-scale genetic...

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Bibliographic Details

Published in:	Frontiers in Pharmacology
Main Authors:	Pamela Gan, Muhammad Irfan Bin Hajis, Mazaya Yumna, Jessline Haruman, Husnul Khotimah Matoha, Dian Tri Wahyudi, Santha Silalahi, Dwi Rizky Oktariani, Fitria Dela, Tazkia Annisa, Tessalonika Damaris Ayu Pitaloka, Priscilla Klaresza Adhiwijaya, Rizqi Yanuar Pauzi, Robby Hertanto, Meutia Ayuputeri Kumaheri, Levana Sani, Astrid Irwanto, Ariel Pradipta, Kamonlawan Chomchopbun, Mar Gonzalez-Porta
Format:	Article
Language:	English
Published:	Frontiers Media S.A. 2024-03-01
Subjects:	SNP microarray copy number variation (CNV) calling microarray-based genotyping pharmacogenomics single nucleotide variant (SNV) calling
Online Access:	https://www.frontiersin.org/articles/10.3389/fphar.2024.1349203/full