Author

Catherine de Lara

University of OxfordORCID 0000-0003-2202-0830Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:variant calling· 2 Assay:bulk RNA-seq· 1 Organism:human· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

David BonsalliD· 2 shared Eleanor J. BarnesiD· 2 shared M. Azim AnsariiD· 2 shared Paolo PiazzaiD· 2 shared Philippa Clare MatthewsiD· 2 shared Sheila LumleyiD· 2 shared Amy TrebesiD· 1 shared Anna L. McNaughtoniD· 1 shared

Activity by Year

2019-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 41 mutual co-author links

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2 shared papersGenomics

David BonsallORCID

Mutual co-authors in cluster

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2 papers

Recent·Most cited

GenomicsbioRxivPreprintFeb 20, 2023

Pan-genotypic probe-based enrichment to improve efficiency of Hepatitis B virus sequencing

Sheila Lumley, Daisy L. Jennings, Elizabeth Waddilove…·Philippa Clare Matthews

This paper introduces a pan-genotypic probe-based enrichment method to enhance HBV sequencing efficiency, showing significant increases in HBV read counts and viral load correlation.

6 citations

humanbulk RNA-seq

𝕏 PostBluesky

GenomicsScientific ReportsPeer-reviewedMay 8, 2019

Illumina and Nanopore methods for whole genome sequencing of hepatitis B virus (HBV)

Anna L. McNaughton, Hannah Roberts, David Bonsall…·Philippa Clare Matthews

This paper describes a method to generate full-length HBV genome data using isothermal amplification and sequencing with Nanopore and Illumina, achieving high consensus accuracy and resolving intra-sample variants.

99 citationstop 1%

whole-genome sequencingexperimental assay

𝕏 PostBluesky