Cell2location maps fine-grained cell types in spatial transcriptomics.


Journal

Nature biotechnology
ISSN: 1546-1696
Titre abrégé: Nat Biotechnol
Pays: United States
ID NLM: 9604648

Informations de publication

Date de publication:
05 2022
Historique:
received: 15 11 2020
accepted: 28 10 2021
pubmed: 15 1 2022
medline: 20 5 2022
entrez: 14 1 2022
Statut: ppublish

Résumé

Spatial transcriptomic technologies promise to resolve cellular wiring diagrams of tissues in health and disease, but comprehensive mapping of cell types in situ remains a challenge. Here we present сell2location, a Bayesian model that can resolve fine-grained cell types in spatial transcriptomic data and create comprehensive cellular maps of diverse tissues. Cell2location accounts for technical sources of variation and borrows statistical strength across locations, thereby enabling the integration of single-cell and spatial transcriptomics with higher sensitivity and resolution than existing tools. We assessed cell2location in three different tissues and show improved mapping of fine-grained cell types. In the mouse brain, we discovered fine regional astrocyte subtypes across the thalamus and hypothalamus. In the human lymph node, we spatially mapped a rare pre-germinal center B cell population. In the human gut, we resolved fine immune cell populations in lymphoid follicles. Collectively, our results present сell2location as a versatile analysis tool for mapping tissue architectures in a comprehensive manner.

Identifiants

pubmed: 35027729
doi: 10.1038/s41587-021-01139-4
pii: 10.1038/s41587-021-01139-4
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

661-671

Subventions

Organisme : Wellcome Trust
ID : 213555/Z/18/Z
Pays : United Kingdom

Informations de copyright

© 2022. The Author(s), under exclusive licence to Springer Nature America, Inc.

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Auteurs

Vitalii Kleshchevnikov (V)

Wellcome Sanger Institute, Hinxton, Cambridge, UK.

Artem Shmatko (A)

Wellcome Sanger Institute, Hinxton, Cambridge, UK.
Moscow State University, Leninskie Gory, Moscow, Russia.

Emma Dann (E)

Wellcome Sanger Institute, Hinxton, Cambridge, UK.

Alexander Aivazidis (A)

Wellcome Sanger Institute, Hinxton, Cambridge, UK.

Hamish W King (HW)

Wellcome Sanger Institute, Hinxton, Cambridge, UK.
Centre for Immunobiology, Blizard Institute, Queen Mary University of London, London, UK.

Tong Li (T)

Wellcome Sanger Institute, Hinxton, Cambridge, UK.

Rasa Elmentaite (R)

Wellcome Sanger Institute, Hinxton, Cambridge, UK.

Artem Lomakin (A)

European Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Hinxton, UK.
European Molecular Biology Laboratory, Genome Biology Unit, Heidelberg, Germany.

Veronika Kedlian (V)

Wellcome Sanger Institute, Hinxton, Cambridge, UK.

Adam Gayoso (A)

Center for Computational Biology, University of California, Berkeley, Berkeley CA, USA.

Mika Sarkin Jain (MS)

Wellcome Sanger Institute, Hinxton, Cambridge, UK.
Theory of Condensed Matter, Department of Physics, Cavendish Laboratory, University of Cambridge, Cambridge, UK.

Jun Sung Park (JS)

Wellcome Sanger Institute, Hinxton, Cambridge, UK.
European Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Hinxton, UK.

Lauma Ramona (L)

Wellcome Sanger Institute, Hinxton, Cambridge, UK.

Elizabeth Tuck (E)

Wellcome Sanger Institute, Hinxton, Cambridge, UK.

Anna Arutyunyan (A)

Wellcome Sanger Institute, Hinxton, Cambridge, UK.

Roser Vento-Tormo (R)

Wellcome Sanger Institute, Hinxton, Cambridge, UK.

Moritz Gerstung (M)

European Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Hinxton, UK.
European Molecular Biology Laboratory, Genome Biology Unit, Heidelberg, Germany.

Louisa James (L)

Centre for Immunobiology, Blizard Institute, Queen Mary University of London, London, UK.

Oliver Stegle (O)

Wellcome Sanger Institute, Hinxton, Cambridge, UK. oliver.stegle@embl.de.
European Molecular Biology Laboratory, Genome Biology Unit, Heidelberg, Germany. oliver.stegle@embl.de.
Division of Computational Genomics and Systems Genetics, German Cancer Research Center (DKFZ), Heidelberg, Germany. oliver.stegle@embl.de.

Omer Ali Bayraktar (OA)

Wellcome Sanger Institute, Hinxton, Cambridge, UK. ob5@sanger.ac.uk.

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