Author

Pierre Lepage

McGill UniversityORCID 0000-0001-9735-1509Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Guillaume BourqueiD· 2 shared Jiannis RagoussisiD· 2 shared Mathieu BourgeyiD· 2 shared Robert J. M. EveleighiD· 2 shared Vincent MooseriD· 2 shared Abdulaziz AlmalikiD· 1 shared Abdulraheem AlshareefiD· 1 shared Ali G. GharaviiD· 1 shared

Activity by Year

2021-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 41 mutual co-author links

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2 shared papersGenomics

Guillaume BourqueORCID

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2 papers

Recent·Most cited

Genomicsnpj Genomic MedicinePeer-reviewedFeb 7, 2024

WEGS: a cost-effective sequencing method for genetic studies combining high-depth whole exome and low-depth whole genome

Claude Bhérer, Robert J. M. Eveleigh, Katerina Trajanoska…·Daniel Taliun

WEGS combines low-depth whole genome and high-depth whole exome sequencing to reduce costs while maintaining variant detection accuracy in genetic studies.

15 citations

humanwhole-exome sequencing

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Genetic & Genomic MedicineJournal of Clinical InvestigationPeer-reviewedMay 27, 2021

Failure to replicate the association of rare loss-of-function variants in type I IFN immunity genes with severe COVID-19

Gundula Povysil, Guillaume Butler‐Laporte, Ning Shang…·Krzysztof Kiryluk

The paper investigates the association of rare loss-of-function variants in type I IFN immunity genes with severe COVID-19 and finds no significant association.

76 citationstop 2%

humanwhole-exome sequencing

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