Author

Charles J. Cox

GlaxoSmithKline (United Kingdom)

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

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Genetics· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Assay:whole-genome sequencing· 2 Research Focus:benchmarking· 1 Research Focus:genome assembly· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Annette S. GrossiD· 1 shared Britt I. DrögemölleriD· 1 shared Caroline T. TiemesseniD· 1 shared Clement AdebamowoiD· 1 shared Dana J. FraseriD· 1 shared David TwesigomweiD· 1 shared Faisal M. FadlelmolaiD· 1 shared Francisco‐Javier GamoiD· 1 shared

Activity by Year

2020-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperGenetics

Annette S. GrossORCID

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2 papers

Recent·Most cited

Comparing low-pass sequencing and genotyping for trait mapping in pharmacogenetics

Kaja A. Wasik, Tomaz Berisa, Joseph K. Pickrell, Jeremiah H. Li, Dana J. Fraser, Karen S. King, Charles J. Cox

This study compares low-pass sequencing and genotyping arrays for pharmacogenetic trait mapping, finding that low-pass sequencing at 0.4x coverage achieves comparable imputation accuracy to genotyping arrays.

BMC Genomics · Mar 20, 2021Peer-reviewedGenetics

The extent and impact of variation in ADME genes in sub-Saharan African populations

Jorge da Rocha, Houcemeddine Othman, Gerrit Botha, Laura Cottino, David Twesigomwe, Samah Ahmed, Britt I. Drögemöller, Faisal M. Fadlelmola, Philip Machanick, Mamana Mbiyavanga, Sumir Panji, Galen E.B. Wright, Clement Adebamowo, Mogomotsi Matshaba, Michèle Ramsay, , Scott Hazelhurst

This study characterizes ADME gene variation in sub-Saharan African populations, identifying novel variants and highlighting the need for tailored pharmacogenomic approaches.

bioRxiv · Jun 14, 2020 · PreprintGenetics