| dc.contributor.author | Lummertz da Rocha, Edroaldo | |
| dc.contributor.author | Rowe, R. Grant | |
| dc.contributor.author | Lundin, Vanessa | |
| dc.contributor.author | Malleshaiah, Mohan | |
| dc.contributor.author | Jha, Deepak Kumar | |
| dc.contributor.author | Rambo, Carlos R. | |
| dc.contributor.author | Li, Hu | |
| dc.contributor.author | North, Trista E. | |
| dc.contributor.author | Collins, James J. | |
| dc.contributor.author | Daley, George Q. | |
| dc.date.accessioned | 2018-08-28T16:17:04Z | |
| dc.date.available | 2018-08-28T16:17:04Z | |
| dc.date.issued | 2018-03 | |
| dc.date.submitted | 2017-11 | |
| dc.identifier.issn | 2041-1723 | |
| dc.identifier.uri | http://hdl.handle.net/1721.1/117589 | |
| dc.description.abstract | A 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.sponsorship | National Institute of Diabetes and Digestive and Kidney Diseases (U.S.) (Grant R24DK092760) | en_US |
| dc.description.sponsorship | National Institute of Allergy and Infectious Diseases (U.S.) (Grant R37AI039394) | en_US |
| dc.description.sponsorship | National Heart, Lung, and Blood Institute (Grant UO1-HL100001) | en_US |
| dc.publisher | Nature Publishing Group | en_US |
| dc.relation.isversionof | http://dx.doi.org/10.1038/S41467-018-03214-Y | en_US |
| dc.rights | Creative Commons Attribution 4.0 International License | en_US |
| dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | en_US |
| dc.source | Nature | en_US |
| dc.title | Reconstruction of complex single-cell trajectories using CellRouter | en_US |
| dc.type | Article | en_US |
| dc.identifier.citation | Lummertz 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.department | Massachusetts Institute of Technology. Institute for Medical Engineering & Science | en_US |
| dc.contributor.department | Massachusetts Institute of Technology. Department of Biological Engineering | en_US |
| dc.contributor.department | Massachusetts Institute of Technology. Synthetic Biology Center | en_US |
| dc.contributor.mitauthor | Collins, James J. | |
| dc.relation.journal | Nature Communications | en_US |
| dc.eprint.version | Final published version | en_US |
| dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
| eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
| dc.date.updated | 2018-08-27T18:13:24Z | |
| dspace.orderedauthors | Lummertz 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.terms | N | en_US |
| dc.identifier.orcid | https://orcid.org/0000-0002-5560-8246 | |
| mit.license | PUBLISHER_CC | en_US |