Author

Genevieve Haliburton

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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Genetics· 1 Systems Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Research Focus:dimensionality reduction· 1 Approach:experimental assay· 1 Organism:human· 1 Organism:mouse· 1 Assay:scATAC-seq· 1 Assay:scRNA-seq· 1

Frequent Co-Authors

Alex D. Robertson· 1 shared Ambrose CarriD· 1 shared Angela Oliveira PiscoiD· 1 shared Arathi Mani· 1 shared Brian McCandless· 1 shared Bruce Martin· 1 shared Charlotte Weaver· 1 shared Clement S. Chu· 1 shared

Activity by Year

2017-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperGenetics

Alex D. Robertson

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Author profile →

2 papers

Recent·Most cited

cellxgene: a performant, scalable exploration platform for high dimensional sparse matrices

Colin Megill, Bruce Martin, Charlotte Weaver, Sidney M. Bell, Lia Prins, Seve Badajoz, Brian McCandless, Angela Oliveira Pisco, Marcus Kinsella, Fiona Griffin, Justin T. Kiggins, Genevieve Haliburton, Arathi Mani, Matthew Weiden, Madison I. Dunitz, , Ambrose Carr

cellxgene couples a Python server to a browser-based JavaScript client, letting researchers cross-filter, re-embed, annotate, and test differential expression in datasets of millions of cells.

bioRxiv · Apr 5, 2021 · PreprintSystems Biology✦ In-depth digest

Development and validation of a 36-gene sequencing assay for hereditary cancer risk assessment

Valentina S. Vysotskaia, Gregory J. Hogan, Genevieve M. Gould, Xin Wang, Alex D. Robertson, Kevin R. Haas, Mark R. Theilmann, Lindsay Spurka, Peter V. Grauman, Henry H. Lai, Diana Jeon, Genevieve Haliburton, Matt Leggett, Clement S. Chu, Kevin Iori, , Imran S. Haque

The paper develops and validates a 36-gene sequencing assay for hereditary cancer risk assessment, showing 100% sensitivity and high specificity across mutation types.

PeerJ · Feb 23, 2017Peer-reviewedGenetics