Author

Matthew Mosior

Washington University in St. LouisORCID 0000-0002-9704-408XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioinformatics· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Kilannin KrysiakiD· 2 shared Malachi GriffithiD· 2 shared Obi L. GriffithiD· 2 shared Todd A. FehnigeriD· 2 shared Zachary L. SkidmoreiD· 2 shared Adam WaalkesiD· 1 shared Ajay KhannaiD· 1 shared Alina D. SchmidtiD· 1 shared

Activity by Year

2019-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 39 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Kilannin KrysiakORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicineCancer Research CommunicationsPeer-reviewedNov 1, 2023

Ultra Deep Sequencing Reveals the Mutational Landscape of Classical Hodgkin Lymphoma

Felicia Gomez, Bryan A. Fisk, Joshua F. McMichael…·Obi L. Griffith

This study uses ultra-deep exome sequencing to identify recurrent mutations in classical Hodgkin lymphoma HRS cells, demonstrating its utility for analyzing genomic variants in large patient cohorts.

16 citations

humanwhole-exome sequencing

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BioinformaticsJCO Clinical Cancer InformaticsPeer-reviewedOct 16, 2019

Identification of community-consensus clinically relevant variants and development of single molecule molecular inversion probes using the CIViC database

Erica Kay Barnell, Adam Waalkes, Matthew Mosior…·Obi L. Griffith

The paper designs single molecule molecular inversion probes targeting clinically relevant variants using the CIViC database, demonstrating high sensitivity and discovering missed variants in cancer samples.

7 citations

humanwhole-exome sequencing

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