Author

Xiaozhong Qian

Bristol-Myers Squibb (United States)ORCID 0009-0002-5951-2230Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genomics· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Ariella SassoniD· 1 shared Hao TangiD· 1 shared Megan Wind‐RotoloiD· 1 shared Natallia KalinavaiD· 1 shared Rafael AldanaiD· 1 shared Sander Y.A. RodenburgiD· 1 shared Sjoerd van HageniD· 1 shared Stefan A. KiroviD· 1 shared

Activity by Year

2020-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenomics

Ariella SassonORCID

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1 paper

Recent·Most cited

GenomicsCancer ResearchPeer-reviewedOct 28, 2020

Mis-annotated multi nucleotide variants in public cancer genomics datasets can lead to inaccurate mutation calls with significant implications

Sujaya Srinivasan, Natallia Kalinava, Rafael Aldana…·Stefan A. Kirov

The paper identifies mis-annotated multi-nucleotide variants (MNVs) in cancer genomics datasets, showing they lead to incorrect amino acid change predictions and recommends merging SNVs into MNVs for accurate variant annotation.

17 citations

humanwhole-exome sequencing

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