Precise identification of cancer cells from allelic imbalances in single cell transcriptomes.


Journal

Communications biology
ISSN: 2399-3642
Titre abrégé: Commun Biol
Pays: England
ID NLM: 101719179

Informations de publication

Date de publication:
07 09 2022
Historique:
received: 10 01 2022
accepted: 05 08 2022
entrez: 7 9 2022
pubmed: 8 9 2022
medline: 11 9 2022
Statut: epublish

Résumé

A fundamental step of tumour single cell mRNA analysis is separating cancer and non-cancer cells. We show that the common approach to separation, using shifts in average expression, can lead to erroneous biological conclusions. By contrast, allelic imbalances representing copy number changes directly detect the cancer genotype and accurately separate cancer from non-cancer cells. Our findings provide a definitive approach to identifying cancer cells from single cell mRNA sequencing data.

Identifiants

pubmed: 36071103
doi: 10.1038/s42003-022-03808-9
pii: 10.1038/s42003-022-03808-9
pmc: PMC9452529
doi:

Substances chimiques

RNA, Messenger 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

884

Subventions

Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 223135/Z/21/Z
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 206194
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 108413/A/15/D
Pays : United Kingdom

Informations de copyright

© 2022. The Author(s).

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Auteurs

Mi K Trinh (MK)

Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.

Clarissa N Pacyna (CN)

Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.

Gerda Kildisiute (G)

Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.

Christine Thevanesan (C)

University College London Great Ormond Street Institute of Child Health, London, UK.

Alice Piapi (A)

University College London Great Ormond Street Institute of Child Health, London, UK.

Kirsty Ambridge (K)

Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.

Nathaniel D Anderson (ND)

Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.

Eleonora Khabirova (E)

Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.

Elena Prigmore (E)

Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.

Karin Straathof (K)

University College London Great Ormond Street Institute of Child Health, London, UK.

Sam Behjati (S)

Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK. sb31@sanger.ac.uk.
Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK. sb31@sanger.ac.uk.
Department of Paediatrics, University of Cambridge, Cambridge, UK. sb31@sanger.ac.uk.

Matthew D Young (MD)

Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK. my4@sanger.ac.uk.

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Classifications MeSH