Author

Geraldine A. Van der Auwera

Broad InstituteORCID 0000-0001-9751-7820Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Eric BanksiD· 2 shared Alessandro CulottiiD· 1 shared Alexander Baumann· 1 shared Alexander OstrovskyiD· 1 shared Alexandru MahmoudiD· 1 shared Allie Hajian· 1 shared Ami Levy‐Moonshine· 1 shared Ana Stevens· 1 shared

Activity by Year

2018-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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2 shared papersBioinformatics

Eric BanksORCID

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2 papers

Recent·Most cited

BioinformaticsCell GenomicsPeer-reviewedJan 1, 2022

Inverting the model of genomics data sharing with the NHGRI Genomic Data Science Analysis, Visualization, and Informatics Lab-space (AnVIL)

Michael C. Schatz, Anthony Philippakis, Enis Afgan…·Jason Walker

The paper describes AnVIL, a cloud-based platform that enables genomic data analysis without data transfer, improving security, scalability, and collaboration.

144 citationstop 1%

experimental assaydatabase / resource

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GenomicsbioRxivPreprintJul 24, 2018

✦ In-depth digest

Scaling accurate genetic variant discovery to tens of thousands of samples

Ryan E. Poplin, Valentín Ruano-Rubio, Mark A. DePristo…·Eric Banks

Per-sample assembly with gVCF output, followed by joint genotyping, lets GATK HaplotypeCaller scale linearly with cohort size while calling indels more accurately than SAMtools, UnifiedGenotyper or Platypus.

1,941 citations

humanwhole-genome sequencing

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