Author

Weicheng Ren

Karolinska InstitutetORCID 0000-0002-7874-825XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Assay:bulk RNA-seq· 1 Research Focus:database / resource· 1 Research Focus:differential expression· 1 Organism:human· 1 Approach:machine learning (classical)· 1 Research Focus:software / tool· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Anne PueliD· 1 shared Bertrand BoissoniD· 1 shared D.N. CooperiD· 1 shared Jean‐Laurent CasanovaiD· 1 shared Juan LiiD· 1 shared Laurent AbeliD· 1 shared Peng ZhangiD· 1 shared Pere Soler‐PalacíniD· 1 shared

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2022-2022 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

Anne PuelORCID

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1 paper

Recent·Most cited

GeneticsProceedings of the National Academy of SciencesPeer-reviewedOct 28, 2022

Genome-wide detection of human variants that disrupt intronic branchpoints

Peng Zhang, Quentin Philippot, Weicheng Ren…·Jean‐Laurent Casanova

The paper introduces BPHunter, a computational tool to detect intronic variants disrupting branchpoints, identifies known and novel mutations, and validates them experimentally.

43 citations

humanbulk RNA-seq

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