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dc.contributor.authorLummertz da Rocha, Edroaldo
dc.contributor.authorRowe, R. Grant
dc.contributor.authorLundin, Vanessa
dc.contributor.authorMalleshaiah, Mohan
dc.contributor.authorJha, Deepak Kumar
dc.contributor.authorRambo, Carlos R.
dc.contributor.authorLi, Hu
dc.contributor.authorNorth, Trista E.
dc.contributor.authorCollins, James J.
dc.contributor.authorDaley, George Q.
dc.date.accessioned2018-08-28T16:17:04Z
dc.date.available2018-08-28T16:17:04Z
dc.date.issued2018-03
dc.date.submitted2017-11
dc.identifier.issn2041-1723
dc.identifier.urihttp://hdl.handle.net/1721.1/117589
dc.description.abstractA better understanding of the cell-fate transitions that occur in complex cellular ecosystems in normal development and disease could inform cell engineering efforts and lead to improved therapies. However, a major challenge is to simultaneously identify new cell states, and their transitions, to elucidate the gene expression dynamics governing cell-type diversification. Here, we present CellRouter, a multifaceted single-cell analysis platform that identifies complex cell-state transition trajectories by using flow networks to explore the subpopulation structure of multi-dimensional, single-cell omics data. We demonstrate its versatility by applying CellRouter to single-cell RNA sequencing data sets to reconstruct cell-state transition trajectories during hematopoietic stem and progenitor cell (HSPC) differentiation to the erythroid, myeloid and lymphoid lineages, as well as during re-specification of cell identity by cellular reprogramming of monocytes and B-cells to HSPCs. CellRouter opens previously undescribed paths for in-depth characterization of complex cellular ecosystems and establishment of enhanced cell engineering approaches.en_US
dc.description.sponsorshipNational Institute of Diabetes and Digestive and Kidney Diseases (U.S.) (Grant R24DK092760)en_US
dc.description.sponsorshipNational Institute of Allergy and Infectious Diseases (U.S.) (Grant R37AI039394)en_US
dc.description.sponsorshipNational Heart, Lung, and Blood Institute (Grant UO1-HL100001)en_US
dc.publisherNature Publishing Groupen_US
dc.relation.isversionofhttp://dx.doi.org/10.1038/S41467-018-03214-Yen_US
dc.rightsCreative Commons Attribution 4.0 International Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.sourceNatureen_US
dc.titleReconstruction of complex single-cell trajectories using CellRouteren_US
dc.typeArticleen_US
dc.identifier.citationLummertz da Rocha, Edroaldo, et al. “Reconstruction of Complex Single-Cell Trajectories Using CellRouter.” Nature Communications 9, 1 (March 2018): 892 © 2018 The Author(s)en_US
dc.contributor.departmentMassachusetts Institute of Technology. Institute for Medical Engineering & Scienceen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Synthetic Biology Centeren_US
dc.contributor.mitauthorCollins, James J.
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.updated2018-08-27T18:13:24Z
dspace.orderedauthorsLummertz da Rocha, Edroaldo; Rowe, R. Grant; Lundin, Vanessa; Malleshaiah, Mohan; Jha, Deepak Kumar; Rambo, Carlos R.; Li, Hu; North, Trista E.; Collins, James J.; Daley, George Q.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-5560-8246
mit.licensePUBLISHER_CCen_US


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