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CellRank for directed single-cell fate mapping

Computational trajectory inference enables the reconstruction of cell state dynamics from single-cell RNA sequencing experiments. However, trajectory inference requires that the direction of a biological process is known, largely limiting its application to differentiating systems in normal developm...

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Autores principales: Lange, Marius, Bergen, Volker, Klein, Michal, Setty, Manu, Reuter, Bernhard, Bakhti, Mostafa, Lickert, Heiko, Ansari, Meshal, Schniering, Janine, Schiller, Herbert B., Pe’er, Dana, Theis, Fabian J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8828480/
https://www.ncbi.nlm.nih.gov/pubmed/35027767
http://dx.doi.org/10.1038/s41592-021-01346-6
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author Lange, Marius
Bergen, Volker
Klein, Michal
Setty, Manu
Reuter, Bernhard
Bakhti, Mostafa
Lickert, Heiko
Ansari, Meshal
Schniering, Janine
Schiller, Herbert B.
Pe’er, Dana
Theis, Fabian J.
author_facet Lange, Marius
Bergen, Volker
Klein, Michal
Setty, Manu
Reuter, Bernhard
Bakhti, Mostafa
Lickert, Heiko
Ansari, Meshal
Schniering, Janine
Schiller, Herbert B.
Pe’er, Dana
Theis, Fabian J.
author_sort Lange, Marius
collection PubMed
description Computational trajectory inference enables the reconstruction of cell state dynamics from single-cell RNA sequencing experiments. However, trajectory inference requires that the direction of a biological process is known, largely limiting its application to differentiating systems in normal development. Here, we present CellRank (https://cellrank.org) for single-cell fate mapping in diverse scenarios, including regeneration, reprogramming and disease, for which direction is unknown. Our approach combines the robustness of trajectory inference with directional information from RNA velocity, taking into account the gradual and stochastic nature of cellular fate decisions, as well as uncertainty in velocity vectors. On pancreas development data, CellRank automatically detects initial, intermediate and terminal populations, predicts fate potentials and visualizes continuous gene expression trends along individual lineages. Applied to lineage-traced cellular reprogramming data, predicted fate probabilities correctly recover reprogramming outcomes. CellRank also predicts a new dedifferentiation trajectory during postinjury lung regeneration, including previously unknown intermediate cell states, which we confirm experimentally.
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spelling pubmed-88284802022-02-22 CellRank for directed single-cell fate mapping Lange, Marius Bergen, Volker Klein, Michal Setty, Manu Reuter, Bernhard Bakhti, Mostafa Lickert, Heiko Ansari, Meshal Schniering, Janine Schiller, Herbert B. Pe’er, Dana Theis, Fabian J. Nat Methods Article Computational trajectory inference enables the reconstruction of cell state dynamics from single-cell RNA sequencing experiments. However, trajectory inference requires that the direction of a biological process is known, largely limiting its application to differentiating systems in normal development. Here, we present CellRank (https://cellrank.org) for single-cell fate mapping in diverse scenarios, including regeneration, reprogramming and disease, for which direction is unknown. Our approach combines the robustness of trajectory inference with directional information from RNA velocity, taking into account the gradual and stochastic nature of cellular fate decisions, as well as uncertainty in velocity vectors. On pancreas development data, CellRank automatically detects initial, intermediate and terminal populations, predicts fate potentials and visualizes continuous gene expression trends along individual lineages. Applied to lineage-traced cellular reprogramming data, predicted fate probabilities correctly recover reprogramming outcomes. CellRank also predicts a new dedifferentiation trajectory during postinjury lung regeneration, including previously unknown intermediate cell states, which we confirm experimentally. Nature Publishing Group US 2022-01-13 2022 /pmc/articles/PMC8828480/ /pubmed/35027767 http://dx.doi.org/10.1038/s41592-021-01346-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Lange, Marius
Bergen, Volker
Klein, Michal
Setty, Manu
Reuter, Bernhard
Bakhti, Mostafa
Lickert, Heiko
Ansari, Meshal
Schniering, Janine
Schiller, Herbert B.
Pe’er, Dana
Theis, Fabian J.
CellRank for directed single-cell fate mapping
title CellRank for directed single-cell fate mapping
title_full CellRank for directed single-cell fate mapping
title_fullStr CellRank for directed single-cell fate mapping
title_full_unstemmed CellRank for directed single-cell fate mapping
title_short CellRank for directed single-cell fate mapping
title_sort cellrank for directed single-cell fate mapping
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8828480/
https://www.ncbi.nlm.nih.gov/pubmed/35027767
http://dx.doi.org/10.1038/s41592-021-01346-6
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