Author

Kevin Eng

Pacific Biosciences (United States)ORCID 0000-0002-7076-5397Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Kevin Eng1 paper · Rutgers, The State University of New Jersey

Biology Disciplines

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Genomics· 2 Bioinformatics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Assay:long-read sequencing· 2 Research Focus:variant calling· 2 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Approach:statistical model· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Aaron M. WengeriD· 1 shared Andrew J. OlsoniD· 1 shared Bo WangiD· 1 shared C.‐W. Pyo· 1 shared Christine C. Lambert· 1 shared Cynthia Vierra‐Green· 1 shared Daniel E. GeraghtyiD· 1 shared Daryl M. WaggottiD· 1 shared

Activity by Year

2017-2020 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 12 mutual co-author links

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1 shared paperGenomics

Aaron M. WengerORCID

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3 papers

Recent·Most cited

Variant Phasing and Haplotypic Expression from Single-molecule Long-read Sequencing in Maize

Bo Wang, Elizabeth Tseng, Primo A. Baybayan, Kevin Eng, Michael Regulski, Yinping Jiao, Liya Wang, Andrew J. Olson, Kapeel M. Chougule, Peter Van Buren, Doreen Ware

The paper develops a tool for haplotype phasing and expression analysis in maize using single-molecule long-read sequencing, revealing allele-specific and imprinted gene expression.

Communications Biology · Feb 18, 2020Peer-reviewedBioinformatics

Long-read whole genome sequencing identifies causal structural variation in a Mendelian disease

Jason D. Merker, Aaron M. Wenger, Tam P. Sneddon, Megan E. Grove, Zachary Zappala, Laure Frésard, Daryl M. Waggott, Sowmi Utiramerur, Yanli Hou, Kevin S. Smith, Stephen B. Montgomery, Matthew Thomas Wheeler, Jillian G. Buchan, Christine C. Lambert, Kevin Eng, , Euan Angus Ashley

The paper uses long-read whole genome sequencing to identify a pathogenic structural variant in a patient with Carney complex, demonstrating the potential of LRS in diagnosing Mendelian diseases.

Genetics in Medicine · Jun 22, 2017Peer-reviewedGenomics

Revealing Complete Complex KIR Haplotypes Phased By Long-Read Sequencing Technology

David Roe, Cynthia Vierra‐Green, C.‐W. Pyo, Kevin Eng, Richard J. Hall, R Kuang, Stephen R. Spellman, Swati Ranade, Daniel E. Geraghty, Martin J. Maiers

The paper uses long-read sequencing to phase and sequence sixteen KIR haplotypes from eight individuals, revealing novel structures and variants.

Genes and Immunity · Jun 1, 2017Peer-reviewedGenomics