2022
DOI: 10.1016/j.jmoldx.2021.12.011
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CYP2C8, CYP2C9, and CYP2C19 Characterization Using Next-Generation Sequencing and Haplotype Analysis

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Cited by 27 publications
(35 citation statements)
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“…The comparisons were done on a sizeable GeT-RM set of publicly available samples and genes for which genotyping panel validations were available (Pratt et al, 2010(Pratt et al, , 2016aGaedigk et al, 2019). These samples were sequenced with three technologies: (1) PGRNseq v.3 Illumina-based pharmacogene-targeted panel (Gordon et al (2016); 137 samples), (2) Illumina whole-genome sequencing (WGS; 70 samples), and (3) 10X Genomics sequencing (95 samples). In addition to these samples, we also ran Aldy on the set of 45 Coriell samples sequenced by PacBio HiFi pharmacogene-targeted panel (Portik et al, 2021;Kingan et al, 2022) and validated by Scott et al (2021).…”
Section: Resultsmentioning
confidence: 99%
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“…The comparisons were done on a sizeable GeT-RM set of publicly available samples and genes for which genotyping panel validations were available (Pratt et al, 2010(Pratt et al, , 2016aGaedigk et al, 2019). These samples were sequenced with three technologies: (1) PGRNseq v.3 Illumina-based pharmacogene-targeted panel (Gordon et al (2016); 137 samples), (2) Illumina whole-genome sequencing (WGS; 70 samples), and (3) 10X Genomics sequencing (95 samples). In addition to these samples, we also ran Aldy on the set of 45 Coriell samples sequenced by PacBio HiFi pharmacogene-targeted panel (Portik et al, 2021;Kingan et al, 2022) and validated by Scott et al (2021).…”
Section: Resultsmentioning
confidence: 99%
“…There are still some open questions left that need to be answered in future work. Most importantly, the panel-validated calls improved by the star-allele callers through the use of HTS data—often containing novel alleles not previously cataloged in the existing databases—need to be validated in a wet-lab environment for all genes presented, as was done recently for a selection of CYP2C genes (Gaedigk et al ., 2022). More tests are also needed on larger cohorts to accurately evaluate the precision of these tools, Aldy 4 included, on rare fusions.…”
Section: Discussionmentioning
confidence: 99%
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“…Subjects were sequenced at the CMH Genomic Medicine Center using ADMEseq, a custom gene panel from Integrated DNA Technologies targeting 289 genes relevant to drug absorption, disposition, metabolism, and excretion, and variants were retrieved as described in detail elsewhere. 21 Variants were manually reviewed. Haplotype (star allele) calls for CYP2C8 and CYP2C9 are according to PharmVar ( https://www.pharmvar.org/ ), 22 , 23 and those for UGT1A1, UGT1A9 and UGT2B7 are according to UGT nomenclature ( https://www.pharmacogenomics.pha.ulaval.ca/ugt‐alleles‐nomenclature/ ).…”
Section: Methodsmentioning
confidence: 99%