Author

Sheila Chandran

Broad Institute

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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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

Ami Levy‐Moonshine· 1 shared Benjamin M. NealeiD· 1 shared Chris Whelan· 1 shared Daniel G. MacArthuriD· 1 shared David E. KlingiD· 1 shared David Roazen· 1 shared Eric BanksiD· 1 shared Geraldine A. Van der AuweraiD· 1 shared

Activity by Year

2018-2018 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenomics

Ami Levy‐Moonshine

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1 paper

Recent·Most cited

Scaling accurate genetic variant discovery to tens of thousands of samples

Ryan E. Poplin, Valentín Ruano-Rubio, Mark A. DePristo, Tim J. Fennell, Mauricio O. Carneiro, Geraldine A. Van der Auwera, David E. Kling, Laura Doyle Gauthier, Ami Levy‐Moonshine, David Roazen, Khalid Shakir, Joel Thibault, Sheila Chandran, Chris Whelan, Monkol Lek, , 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.

bioRxiv · Jul 24, 2018 · PreprintGenomics✦ In-depth digest