Author

Will Salerno

Baylor College of Medicine

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Bioinformatics· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

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

Frequent Co-Authors

Hyun Min KangiD· 2 shared Adam C. EnglishiD· 1 shared Adam E. LockeiD· 1 shared Alan R. ShuldineriD· 1 shared Allison RegieriD· 1 shared Amy DamaskiD· 1 shared Aris BarasiD· 1 shared Benjamin M. NealeiD· 1 shared

Activity by Year

2018-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersGenetic & Genomic Medicine

Hyun Min KangORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Exome sequencing of 628,388 individuals identifies common and rare variant associations with clonal hematopoiesis phenotypes

Michael D. Kessler, Amy Damask, Sean O’Keeffe, Michael Van Meter, Nilanjana Banerjee, Stefan Semrau, Dadong Li, Kyoko Watanabe, Julie E. Horowitz, Yariv J. Houvras, Christopher E. Gillies, Joelle S. Mbatchou, Ryan R. White, Jack A. Kosmicki, Michelle G. LeBlanc, , Eric Jorgenson

This study uses exome sequencing of 628,388 individuals to identify genetic variants associated with clonal hematopoiesis and its health outcomes.

medRxiv · Dec 29, 2021 · PreprintGenetic & Genomic Medicine

Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects

Allison Regier, Yossi Farjoun, David E. Larson, Olga A. Krasheninina, Hyun Min Kang, Daniel P. Howrigan, Bo-Juen Chen, Manisha Kher, Eric Banks, Darren C. Ames, Adam C. English, Heng Li, Jinchuan Xing, Yeting Zhang, Tara Cox Matise, , Ira M. Hall

The paper defines functional equivalence standards for genome sequencing pipelines to enable harmonized variant calling across diverse datasets with minimal batch effects.

Nature Communications · Sep 26, 2018Peer-reviewedBioinformatics