Author

Piotr Kaleta

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

Biology Disciplines

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Genomics· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Dale MuzzeyiD· 1 shared Hyunseok Peter KangiD· 1 shared Jillian I. Johnson· 1 shared Kaylene J. Ready· 1 shared Kelly A. Pierce· 1 shared Kevin R. Haas· 1 shared Laura M. MelroyiD· 1 shared Shera F. KashiD· 1 shared

Activity by Year

2018-2018 · peak 1/yr

Co-Author Collaboration Network

8 top collaborators · 28 mutual co-author links

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1 shared paperGenomics

Dale MuzzeyORCID

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1 paper

Recent·Most cited

Software-assisted manual review of clinical NGS data:an alternative to routine Sanger sequencing confirmationwith equivalent results in >15,000 hereditary cancer screens

Dale Muzzey, Shera F. Kash, Jillian I. Johnson, Laura M. Melroy, Piotr Kaleta, Kelly A. Pierce, Kaylene J. Ready, Hyunseok Peter Kang, Kevin R. Haas

The paper demonstrates that software-assisted manual review of NGS data achieves equivalent accuracy to Sanger sequencing in confirming variant calls for hereditary cancer screening.

bioRxiv · Sep 23, 2018 · PreprintGenomics