Author

Kenneth Eng

NewYork–Presbyterian HospitalORCID 0000-0001-9818-8299Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:variant calling· 2 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Andrea SboneriD· 2 shared Juan Miguel MosqueraiD· 2 shared Olivier ElementoiD· 2 shared Aditya S. DeshpandeiD· 1 shared Adrian Y. TaniD· 1 shared Alessandro RomaneliD· 1 shared Anne‐Katrin EmdeiD· 1 shared Brian J. ReidiD· 1 shared

Activity by Year

2017-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 35 mutual co-author links

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2 shared papersGenomics

Andrea SbonerORCID

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2 papers

Recent·Most cited

GenomicsbioRxivPreprintNov 12, 2019

Novel patterns of complex structural variation revealed across thousands of cancer genome graphs

Kevin Hadi, Xiaotong Yao, Julie M. Behr…·Marcin B. Imielinski

The paper identifies three novel complex structural variation patterns in cancer genomes using genome graph analysis across 2,833 tumor WGS.

14 citations

humanwhole-genome sequencing

𝕏 PostBluesky

GenomicsbioRxivPreprintMar 1, 2017

Discovery and reporting of clinically-relevant germline variants in advanced cancer patients assessed using whole-exome sequencing

Tuo Zhang, Alessandro Romanel, Kenneth Eng…·Olivier Elemento

This study reports that 17% of advanced cancer patients have clinically relevant germline variants, with higher rates of cancer-associated variants compared to control cohorts.

2 citations

humanwhole-exome sequencing

𝕏 PostBluesky