Author

Gang Wang

The University of Texas MD Anderson Cancer CenterORCID 0009-0003-5202-2025Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Gang Wang9 papers · BC Cancer Agency

Biology Disciplines

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Systems Biology· 2 Bioinformatics· 1

Signature Assays, Organisms & Methods

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Assay:CRISPR screen· 3 Organism:human· 3 Research Focus:perturbation response prediction· 2 Approach:statistical model· 2 Approach:deep learning· 1 Research Focus:drug response / drug discovery· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Traver HartiD· 3 shared Medina ColiciD· 2 shared Sanjana SrinivasaniD· 2 shared W. Frank LenoiriD· 2 shared Angela K. DeemiD· 1 shared Chieh-Yuan LiiD· 1 shared Chris Bristow· 1 shared Daniel DurocheriD· 1 shared

Activity by Year

2019-2019 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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3 shared papersSystems Biology

Traver HartORCID

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3 papers

Recent·Most cited

Systems BiologyNature CommunicationsPeer-reviewedJul 17, 2019

Multiplexed pooled library screening with Cpf1

Jintan Liu, Sanjana Srinivasan, Chieh-Yuan Li…·Giulio Francesco Draetta

The paper develops a multiplexed CRISPR/Cas9-based screening strategy using AsCpf1 to create a smaller, more efficient genome-wide knockout library.

44 citations

humanCRISPR screen

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Systems BiologyLife Science AlliancePeer-reviewedApr 1, 2019

Hierarchical organization of the human cell from a cancer coessentiality network

Eiru Kim, Merve Dede, W. Frank Lenoir…·Traver Hart

The paper constructs a coessentiality network from CRISPR knockout screens to infer gene function and reveal hierarchical cell organization.

90 citationstop 4%

humanCRISPR screen

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BioinformaticsbioRxivPreprintMar 11, 2019

Identifying chemogenetic interactions from CRISPR knockout screens with drugZ

Medina Colic, Gang Wang, Michal Zimmermann…·Traver Hart

drugZ identifies chemogenetic interactions from CRISPR screens, finding more homologous recombination repair pathway genes and confirming KEAP1 loss as a resistance factor for ERK inhibitors.

17 citations

humanCRISPR screen

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