| Literature DB >> 35027767 |
Marius Lange1,2, Volker Bergen1,2, Michal Klein1, Manu Setty3,4, Bernhard Reuter5,6, Mostafa Bakhti7,8, Heiko Lickert7,8, Meshal Ansari1,9, Janine Schniering9, Herbert B Schiller9, Dana Pe'er10, Fabian J Theis11,12,13.
Abstract
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.Entities:
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Year: 2022 PMID: 35027767 PMCID: PMC8828480 DOI: 10.1038/s41592-021-01346-6
Source DB: PubMed Journal: Nat Methods ISSN: 1548-7091 Impact factor: 28.547