Author

Jennifer Becq

Illumina (United Kingdom)

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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Bioinformatics· 1 Genetic & Genomic Medicine· 1

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

Mark T. RossiD· 2 shared Agata Stodolna· 1 shared Andrew David BeggsiD· 1 shared Anthony V. MoormaniD· 1 shared Christine J. HarrisoniD· 1 shared Claire FieldingiD· 1 shared Daniel BlakewayiD· 1 shared David Bentley· 1 shared

Activity by Year

2021-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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2 shared papersBioinformatics

Mark T. RossORCID

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Author profile →

2 papers

Recent·Most cited

A dedicated caller for DUX4 rearrangements from whole-genome sequencing data

Pascal Grobecker, Stefano Berri, John F. Peden, Kai-Jie Chow, Claire Fielding, Ivana Armogida, Helen Northen, David J. McBride, Peter J. Campbell, Jennifer Becq, Sarra L. Ryan, David Bentley, Christine J. Harrison, Anthony V. Moorman, Mark T. Ross, Martina Mijušković

The paper introduces a software tool to detect DUX4 rearrangements from whole-genome sequencing data, showing it can identify known and previously unidentified cases in a cohort of paediatric ALL patients.

bioRxiv · May 23, 2024 · PreprintBioinformatics

Clinical-grade whole genome sequencing of colorectal cancer and 3-prime transcriptome analysis demonstrate targetable alterations in the majority of patients.

Agata Stodolna, Miao He, Mahesh Vasipalli, Zoya Kingsbury, Jennifer Becq, Joanne Stockton, Mark Dilworth, Jonathan James, Toju Sillo, Daniel Blakeway, Steve Ward, Tariq Ismail, Mark T. Ross, Andrew David Beggs

The paper uses clinical-grade whole genome sequencing and 3' transcriptome analysis to identify targetable genomic alterations in colorectal cancer patients.

Genome Medicine · Feb 25, 2021Peer-reviewedGenetic & Genomic Medicine