Author

Chris Miller

AbbVie (United States)Primary ORCID profile (0000-0002-5957-7088 · 1 paper)Unclaimed ORCID profile · follow to get notified of new preprints

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Chris MilleriD1 paper · University of Manchester

Biology Disciplines

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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Ali Moshrefi· 1 shared Ana Granat· 1 shared Andreas SchereriD· 1 shared Aparna Natarajan· 1 shared Arati RaziuddiniD· 1 shared Ashley Walton· 1 shared Baitang NingiD· 1 shared Bao Quoc TraniD· 1 shared

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2021-2021 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperGenomics

Ali Moshrefi

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1 paper

Recent·Most cited

GenomicsNature BiotechnologyPeer-reviewedSep 1, 2021

Achieving reproducibility and accuracy in cancer mutation detection with whole-genome and whole-exome sequencing

Wenming Xiao, Luyao Ren, Zhong Chen…·Leming M. Shi

This study evaluates reproducibility and accuracy of cancer mutation detection using whole-genome and whole-exome sequencing across multiple sequencing centers and bioinformatics pipelines.

192 citationstop 1%

humanwhole-genome sequencing

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