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dc.contributor.authorYang, Karren Dai
dc.contributor.authorDamodaran, Karthik
dc.contributor.authorVenkatachalapathy, Saradha
dc.contributor.authorSoylemezoglu, Ali C.
dc.contributor.authorShivashankar, G.V.
dc.contributor.authorUhler, Caroline
dc.date.accessioned2021-04-13T19:55:50Z
dc.date.available2021-04-13T19:55:50Z
dc.date.issued2020-04
dc.date.submitted2019-10
dc.identifier.issn1553-7358
dc.identifier.urihttps://hdl.handle.net/1721.1/130470
dc.description.abstractThis is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Lineage tracing involves the identification of all ancestors and descendants of a given cell, and is an important tool for studying biological processes such as development and disease progression. However, in many settings, controlled time-course experiments are not feasible, for example when working with tissue samples from patients. Here we present ImageAEOT, a computational pipeline based on autoencoders and optimal transport for predicting the lineages of cells using time-labeled datasets from different stages of a cellular process. Given a single-cell image from one of the stages, ImageAEOT generates an artificial lineage of this cell based on the population characteristics of the other stages. These lineages can be used to connect subpopulations of cells through the different stages and identify image-based features and biomarkers underlying the biological process. To validate our method, we apply ImageAEOT to a benchmark task based on nuclear and chromatin images during the activation of fibroblasts by tumor cells in engineered 3D tissues. We further validate ImageAEOT on chromatin images of various breast cancer cell lines and human tissue samples, thereby linking alterations in chromatin condensation patterns to different stages of tumor progression. Our results demonstrate the promise of computational methods based on autoencoding and optimal transport principles for lineage tracing in settings where existing experimental strategies cannot be used.en_US
dc.description.sponsorshipONR (Grant N00014-18-1-2765)en_US
dc.language.isoen
dc.publisherPublic Library of Science (PLoS)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1371/journal.pcbi.1007828en_US
dc.rightsCreative Commons Attribution 4.0 International licenseen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourcePLoSen_US
dc.titlePredicting cell lineages using autoencoders and optimal transporten_US
dc.typeArticleen_US
dc.identifier.citationYang, Karren Dai et al. "Predicting cell lineages using autoencoders and optimal transport." PLoS Computational Biology 16, 4 (April 2020): e1007828 © 2020 Yang et al.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Institute for Data, Systems, and Societyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Electrical Engineering and Computer Scienceen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.relation.journalPLoS Computational Biologyen_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.updated2021-03-19T15:06:50Z
dspace.orderedauthorsYang, KD; Damodaran, K; Venkatachalapathy, S; Soylemezoglu, AC; Shivashankar, GV; Uhler, Cen_US
dspace.date.submission2021-03-19T15:06:51Z
mit.journal.volume16en_US
mit.journal.issue4en_US
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work and Publication Information Needed


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