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dc.contributor.authorSekelja, Monika
dc.contributor.authorPaulsen, Jonas
dc.contributor.authorCollas, Philippe
dc.date.accessioned2016-04-12T05:00:17Z
dc.date.available2016-04-12T05:00:17Z
dc.date.issued2016
dc.identifier.citationGenome Biology. 2016 Apr 07;17(1):54
dc.identifier.urihttp://hdl.handle.net/10852/50087
dc.description.abstractGenome-wide sequencing technologies enable investigations of the structural properties of the genome in various spatial dimensions. Here, we review computational techniques developed to model the three-dimensional genome in single cells versus ensembles of cells and assess their underlying assumptions. We further address approaches to study the spatio-temporal aspects of genome organization from single-cell data.
dc.language.isoeng
dc.rightsSekelja et al.; licensee BioMed Central Ltd.
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.title4D nucleomes in single cells: what can computational modeling reveal about spatial chromatin conformation?
dc.typeJournal article
dc.date.updated2016-04-12T05:00:17Z
dc.creator.authorSekelja, Monika
dc.creator.authorPaulsen, Jonas
dc.creator.authorCollas, Philippe
dc.identifier.doihttp://dx.doi.org/10.1186/s13059-016-0923-2
dc.identifier.urnURN:NBN:no-53764
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/50087/1/13059_2016_Article_923.pdf
dc.type.versionPublishedVersion
cristin.articleid54


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