Concordance between Research Sequencing and Clinical Pharmacogenetic Genotyping in the eMERGE-PGx Study.

The Journal of Molecular Diagnostics : JMD
Laura J Rasmussen-TorvikStuart A Scott

Abstract

There has been extensive debate about both the necessity of orthogonal confirmation of next-generation sequencing (NGS) results in Clinical Laboratory Improvement Amendments-approved laboratories and return of research NGS results to participants enrolled in research studies. In eMERGE-PGx, subjects underwent research NGS using PGRNseq and orthogonal targeted genotyping in clinical laboratories, which prompted a comparison of genotyping results between platforms. Concordance (percentage agreement) was reported for 4077 samples tested across nine combinations of research and clinical laboratories. Retesting was possible on a subset of 1792 samples, and local laboratory directors determined sources of genotype discrepancy. Research NGS and orthogonal clinical genotyping had an overall per sample concordance rate of 0.972 and per variant concordance rate of 0.997. Genotype discrepancies attributed to research NGS were because of sample switching (preanalytical errors), whereas the majority of genotype discrepancies (92.3%) attributed to clinical genotyping were because of allele dropout as a result of rare variants interfering with primer hybridization (analytical errors). These results highlight the analytical quality of clinical...Continue Reading

Citations

May 31, 2018·Cold Spring Harbor Perspectives in Medicine·Ute I SchwarzRichard B Kim
Feb 8, 2019·Pharmacogenomics·Wanqiong QiaoStuart A Scott
Aug 10, 2019·Journal of Personalized Medicine·Catriona Hippman, Corey Nislow
Nov 11, 2020·Molecular Biology and Evolution·Yun-Hua LoWen-Ya Ko
Dec 10, 2020·Genes·Maaike van der LeeJesse J Swen
Oct 3, 2021·Human Genetics·Evangelia Eirini TsermpiniGeorge P Patrinos
Mar 20, 2018·Biomedicine & Pharmacotherapy = Biomédecine & Pharmacothérapie·Xiao ZhangJinming Li

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