Author

Richard Corbett

BC Cancer Agency

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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Genomics· 3 Bioinformatics· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 5 Research Focus:gene regulatory network inference· 4 Assay:whole-genome sequencing· 4 Research Focus:differential expression· 3 Approach:experimental assay· 3 Research Focus:variant calling· 3 Research Focus:database / resource· 2 Approach:statistical model· 2

Frequent Co-Authors

Marco A. MarraiD· 5 shared Richard A. MooreiD· 3 shared Robin CoopeiD· 3 shared Signe MacLennaniD· 3 shared Vanessa PorteriD· 3 shared Andrew J. J. MungalliD· 2 shared Eric Chuah· 2 shared Glenn ChangiD· 2 shared

Activity by Year

2017-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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5 shared papersGenomics

Marco A. MarraORCID

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Author profile →

5 papers

Recent·Most cited

Allele-specific chromatin modifications of HPV-associated extrachromosomal DNAs in cervical cancer

Signe MacLennan, Michelle Ng, Vanessa Porter, Richard Corbett, Pawan K. Pandoh, Diane L.N. Trinh, Robin Coope, Yongjun Zhao, Marco A. Marra

The paper identifies epigenetic differences between HPV-human hybrid and human-only ecDNAs in cervical cancer, showing allele-specific regulation and enhancer activity in hybrid ecDNAs.

bioRxiv · Jul 20, 2026 · PreprintGenomics

Genomic structures and regulation patterns at HPV integration sites in cervical cancer

Vanessa Porter, Michelle Ng, Kieran O’Neill, Signe MacLennan, Richard Corbett, Luka Culibrk, Zeid Hamadeh, Marissa Iden, Rachel Schmidt, Shirng‐Wern Tsaih, Carolyn Nakisige, Martin Origa, Jackson Orem, Glenn Chang, Jeremy Fan, , Marco A. Marra

The paper uses long-read sequencing to analyze HPV integration sites in cervical cancer genomes, identifying structural and epigenetic impacts of integration.

Genome Research · Apr 1, 2025Peer-reviewedGenomics

Long-read sequencing of an advanced cancer cohort resolves rearrangements, unravels haplotypes, and reveals methylation landscapes

Kieran O’Neill, Erin Pleasance, Jeremy Fan, Vahid Akbari, Glenn Chang, Katherine Dixon, Veronika Csizmók, Signe MacLennan, Vanessa Porter, Andrew Galbraith, Cameron J. Grisdale, Luka Culibrk, John H. Dupuis, Richard Corbett, James Hopkins, , Steven J.M. Jones

This paper presents a long-read sequencing dataset of cancer samples, showing its ability to resolve structural variants, haplotypes, and methylation patterns in precision medicine.

Cell Genomics · Oct 14, 2024Peer-reviewedGenetic & Genomic Medicine

Resource: Scalable whole genome sequencing of 40,000 single cells identifies stochastic aneuploidies, genome replication states and clonal repertoires

Emma Laks, Hans Zahn, Daniel Lai, Andrew McPherson, Adi Steif, Jazmine Brimhall, Justina Biele, Beixi Wang, Tehmina Masud, Diljot S. Grewal, Cydney B Nielsen, Samantha Leung, Viktoria Bojilova, Maia A. Smith, Oleg Golovko, , Samuel A. J. R. Aparicio

bioRxiv · Sep 13, 2018 · PreprintGenomics

Comprehensive characterization of genomic, transcriptomic and epigenomic artifacts introduced in formalin-fixed, paraffin-embedded tissues.

Erik J. Zmuda, Kyle R Covington, Cyriac Kandoth, Charlotte K.Y. Ng, Daniel J Weisenberger, Reanne Bowlby, Andy Chu, Richard Corbett, Denise Brooks, Andrew D. Cherniack, Bradley Murray, Shiyun Ling, Wei Zhao, Eve Shinbrot, Raymond S Lim, , Katherine A Hoadley

This study characterizes genomic, transcriptomic, and epigenomic artifacts in FFPE tissues and provides best practices to mitigate their impact on molecular analysis.

Cancer Genetics · Jun 6, 2017Peer-reviewedBioinformatics