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dc.contributor.authorYeo, Grace Hui Ting
dc.contributor.authorSaksena, Sachit D
dc.contributor.authorGifford, David K
dc.date.accessioned2022-06-28T13:36:55Z
dc.date.available2022-06-28T13:36:55Z
dc.date.issued2021
dc.identifier.urihttps://hdl.handle.net/1721.1/143571
dc.description.abstractAbstract Existing computational methods that use single-cell RNA-sequencing (scRNA-seq) for cell fate prediction do not model how cells evolve stochastically and in physical time, nor can they predict how differentiation trajectories are altered by proposed interventions. We introduce PRESCIENT (Potential eneRgy undErlying Single Cell gradIENTs), a generative modeling framework that learns an underlying differentiation landscape from time-series scRNA-seq data. We validate PRESCIENT on an experimental lineage tracing dataset, where we show that PRESCIENT is able to predict the fate biases of progenitor cells in hematopoiesis when accounting for cell proliferation, improving upon the best-performing existing method. We demonstrate how PRESCIENT can simulate trajectories for perturbed cells, recovering the expected effects of known modulators of cell fate in hematopoiesis and pancreatic β cell differentiation. PRESCIENT is able to accommodate complex perturbations of multiple genes, at different time points and from different starting cell populations, and is available at t https:// github.com/gifford-lab/prescient.en_US
dc.language.isoen
dc.publisherSpringer Science and Business Media LLCen_US
dc.relation.isversionof10.1038/S41467-021-23518-Wen_US
dc.rightsCreative Commons Attribution 4.0 International licenseen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceNatureen_US
dc.titleGenerative modeling of single-cell time series with PRESCIENT enables prediction of cell trajectories with interventionsen_US
dc.typeArticleen_US
dc.identifier.citationYeo, Grace Hui Ting, Saksena, Sachit D and Gifford, David K. 2021. "Generative modeling of single-cell time series with PRESCIENT enables prediction of cell trajectories with interventions." Nature Communications, 12 (1).
dc.contributor.departmentMassachusetts Institute of Technology. Computer Science and Artificial Intelligence Laboratory
dc.contributor.departmentMassachusetts Institute of Technology. Computational and Systems Biology Program
dc.contributor.departmentMassachusetts Institute of Technology. Department of Electrical Engineering and Computer Science
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineering
dc.relation.journalNature Communicationsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2022-06-28T13:22:38Z
dspace.orderedauthorsYeo, GHT; Saksena, SD; Gifford, DKen_US
dspace.date.submission2022-06-28T13:22:41Z
mit.journal.volume12en_US
mit.journal.issue1en_US
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work and Publication Information Neededen_US


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