Author

Brandon LaBarge

Pennsylvania State University

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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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2

Frequent Co-Authors

James Riley BroachiD· 2 shared Lijun ZhangiD· 2 shared Scott Chartrand· 2 shared Alan Lennon· 1 shared Alex R. HastieiD· 1 shared Andy Wing Chun PangiD· 1 shared Benjamin Clifford· 1 shared Beth A. PiteliD· 1 shared

Activity by Year

2020-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

James Riley BroachORCID

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2 papers

Recent·Most cited

Identification of Somatic Structural Variants in Solid Tumors By Optical Genome Mapping

David Y. Goldrich, Brandon LaBarge, Scott Chartrand, Lijun Zhang, Henry B. Sadowski, Yang Zhang, Khoa Pham, Hannah Way, Chi-Yu Lai, Andy Wing Chun Pang, Benjamin Clifford, Alex R. Hastie, Mark Oldakowski, David Goldenberg, James Riley Broach

This paper describes a method using optical genome mapping to identify somatic structural variants in solid tumors, showing high reliability and functional relevance.

Journal of Personalized Medicine · Feb 18, 2021Peer-reviewedGenetic & Genomic Medicine

A National Multicenter Evaluation of the Clinical Utility of Optical Genome Mapping for Assessment of Genomic Aberrations in Acute Myeloid Leukemia

Brynn Levy, Linda Banovic Baughn, Scott Chartrand, Brandon LaBarge, David F. Claxton, Alan Lennon, Yassmine M. N. Akkari, Claudia P. Cujar, Ravindra B Kolhe, Kate Kroeger, Beth A. Pitel, Nikhil Sahajpal, Malini Sathanoori, George Vlad, Lijun Zhang, , James Riley Broach

This study evaluates optical genome mapping (OGM) for detecting genomic aberrations in AML, finding it identifies all clinically relevant SVs and CNVs and detects additional variants missed by standard methods.

medRxiv · Nov 7, 2020 · PreprintGenetic & Genomic Medicine