Author

Kshithija Nagulapalli

New York Genome Center

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 Approach:statistical model· 2 Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2

Frequent Co-Authors

Michael C. ZodyiD· 2 shared Søren GermeriD· 2 shared Alexi M. RunnelsiD· 1 shared Allison RegieriD· 1 shared André CorveloiD· 1 shared Anna Okula BasileiD· 1 shared Can AlkaniD· 1 shared Charles LeeiD· 1 shared

Activity by Year

2019-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 38 mutual co-author links

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2 shared papersGenomics

Michael C. ZodyORCID

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2 papers

Recent·Most cited

High coverage whole genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios

Marta S. Byrska‐Bishop, Uday S. Evani, Xuefang Zhao, Anna Okula Basile, Haley Abel, Allison Regier, André Corvelo, Wayne E. Clarke, Rajeeva Musunuri, Kshithija Nagulapalli, Susan Fairley, Alexi M. Runnels, Lara Heermans Winterkorn, Ernesto Lowy, Evan E. Eichler, , Michael C. Zody

The paper presents a high coverage whole genome sequencing resource of 3,202 samples, including 602 trios, generated from the expanded 1000 Genomes Project.

Cell · Sep 1, 2022Peer-reviewedGenomics

Deep sequencing of 3 cancer cell lines on 2 sequencing platforms

Kanika S. Arora, Minita J. Shah, Molly E. Johnson, Rashesh Sanghvi, Jennifer Shelton, Kshithija Nagulapalli, Dayna M. Oschwald, Michael C. Zody, Søren Germer, Vaidehi Jobanputra, Jade Carter, Nicolas Robine

The paper benchmarks a new sequencing platform and develops a somatic calling pipeline using deep sequencing of cancer cell lines on two platforms.

Scientific Reports · Dec 13, 2019Peer-reviewedGenomics