Author

Phu Van

ORCID 0000-0001-8605-316XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Andrew WilliamsiD· 2 shared Carole Lyn YaukiD· 2 shared Charles C. ValentineiD· 2 shared Fang Yin LoiD· 2 shared Francesco MarchettiiD· 2 shared Jesse J. SalkiD· 2 shared Annette E. DodgeiD· 1 shared Carol D. Swartz· 1 shared

Activity by Year

2023-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 41 mutual co-author links

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2 shared papersGenomics

Andrew WilliamsORCID

Mutual co-authors in cluster

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2 papers

Recent·Most cited

GenomicsArchives of ToxicologyPeer-reviewedJun 21, 2023

Duplex Sequencing Provides Detailed Characterization of Mutation Frequencies and Spectra in the Bone Marrow of MutaMouse Males Exposed to Procarbazine Hydrochloride

Annette E. Dodge, Danielle P. M. LeBlanc, Gu Zhou…·Francesco Marchetti

This study uses Duplex Sequencing to assess mutation frequencies and spectra in MutaMouse bone marrow after procarbazine exposure, showing its advantages over conventional assays.

42 citationstop 3%

mousewhole-genome sequencing

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GenomicsbioRxivPreprintFeb 22, 2023

Error-corrected Duplex Sequencing enables direct detection and quantification of mutations in human TK6 cells with remarkable inter-laboratory consistency

Eunnara Cho, Carol D. Swartz, Andrew Williams…·Carole Lyn Yauk

This study demonstrates that error-corrected Duplex Sequencing reliably detects and quantifies mutations in human TK6 cells across different laboratories and time points.

2 citations

humanwhole-genome sequencing

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