Author

Victoria Cloke

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 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:variant calling· 2 Approach:deep learning· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Ann Strydom· 2 shared Elise RuarkiD· 2 shared Nazneen RahmaniD· 2 shared Shazia Mahamdallie· 2 shared Sheila Seal· 2 shared Angela George· 1 shared Anthony Renwick· 1 shared Daniel Riddell· 1 shared

Activity by Year

2015-2016 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 39 mutual co-author links

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2 shared papersGenetics

Ann Strydom

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2 papers

Recent·Most cited

GeneticsbioRxivMar 16, 2016

Implementing rapid, robust, cost-effective, patient-centred, routine genetic testing in ovarian cancer patients

Angela George, Daniel Riddell, Sheila Seal…·Mainstreaming Cancer Genetics (MCG) Programme

This study implements a streamlined BRCA gene testing pathway for ovarian cancer patients, achieving high uptake and efficiency with significant cost savings and improved patient outcomes.

DOI 10.1038/srep29506

humanDNA methylation

𝕏 PostBluesky

GenomicsbioRxivMar 21, 2015

CSN and CAVA: variant annotation tools for rapid, robust next-generation sequencing analysis in the clinic

Márton Münz, Elise Ruark, Anthony Renwick…·Nazneen Rahman

This paper introduces CSN and CAVA, tools for standardized, rapid variant annotation of NGS data, showing high accuracy and clinical relevance in BRCA1/BRCA2 analysis.

DOI 10.1186/s13073-015-0195-6

humanwhole-exome sequencing

𝕏 PostBluesky