Author

Jeremy Gollub

Thermo Fisher Scientific (United States)ORCID 0000-0002-3790-7381Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 1

Signature Assays, Organisms & Methods

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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

A Mittal· 1 shared Adrian Bivol· 1 shared Alan H. Roter· 1 shared BA Wong· 1 shared Jeanette P. SchmidtiD· 1 shared Katherine H. AulliD· 1 shared Marcos H. Woehrmann· 1 shared Orna Man· 1 shared

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2021-2021 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

A Mittal

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1 paper

Recent·Most cited

GeneticsbioRxivPreprintSep 13, 2021

Novel genotyping algorithms for rare variants significantly improve the accuracy of Applied Biosystems™ Axiom™ array genotyping calls

Orna Man, Marcos H. Woehrmann, T. A. Webster…·Jeanette P. Schmidt

The paper improves Axiom array genotyping accuracy for rare variants using a new algorithm and probe filtering, increasing positive predictive value and sensitivity across multiple minor allele frequency ranges.

1 citation

humanwhole-exome sequencing

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