Author

Ryan Poplin

Google (United States)

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· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:variant calling· 2 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Research Focus:GWAS / association mapping· 1 Approach:statistical model· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Adam Kiezun· 1 shared Ami Levy Moonshine· 1 shared Andrew Hill· 1 shared Anne O'Donnell-Luria· 1 shared Beryl Cummings· 1 shared Daniel Birnbaum· 1 shared Daniel Howrigan· 1 shared David Cooper· 1 shared

Activity by Year

2016-2018 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenomics

Adam Kiezun

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2 papers

Recent·Most cited

CrowdVariant: a crowdsourcing approach to classify copy number variants

Peyton Greenside, Justin M. Zook, Marc Salit, Ryan Poplin, Madeleine Cule, Mark A. DePristo

The paper introduces CrowdVariant, a crowdsourcing framework to classify copy number variants (CNVs) using NGS data, and identifies 1,781 high-confidence CNVs in a reference sample.

Pacific Symposium on Biocomputing (PSB) · Nov 1, 2018Peer-reviewedGenomics

Analysis of protein-coding genetic variation in 60,706 humans

Exome Aggregation Consortium, Monkol Lek, Konrad Karczewski, Eric Minikel, Kaitlin Samocha, Eric Banks, Timothy Fennell, Anne O'Donnell-Luria, James Ware, Andrew Hill, Beryl Cummings, Taru Tukiainen, Daniel Birnbaum, Jack Kosmicki, Laramie Duncan, , Douglas

This paper analyzes protein-coding genetic variation in 60,706 humans to catalog diversity, assess pathogenicity, and identify genes under strong selection.

Nature · Aug 17, 2016Peer-reviewedGenomics