dc.contributor.author | Sekelja, Monika | |
dc.contributor.author | Paulsen, Jonas | |
dc.contributor.author | Collas, Philippe | |
dc.date.accessioned | 2016-04-12T05:00:17Z | |
dc.date.available | 2016-04-12T05:00:17Z | |
dc.date.issued | 2016 | |
dc.identifier.citation | Genome Biology. 2016 Apr 07;17(1):54 | |
dc.identifier.uri | http://hdl.handle.net/10852/50087 | |
dc.description.abstract | Genome-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.iso | eng | |
dc.rights | Sekelja et al.; licensee BioMed Central Ltd. | |
dc.rights | Attribution 4.0 International | |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | |
dc.title | 4D nucleomes in single cells: what can computational modeling reveal about spatial chromatin conformation? | |
dc.type | Journal article | |
dc.date.updated | 2016-04-12T05:00:17Z | |
dc.creator.author | Sekelja, Monika | |
dc.creator.author | Paulsen, Jonas | |
dc.creator.author | Collas, Philippe | |
dc.identifier.doi | http://dx.doi.org/10.1186/s13059-016-0923-2 | |
dc.identifier.urn | URN:NBN:no-53764 | |
dc.type.document | Tidsskriftartikkel | |
dc.type.peerreviewed | Peer reviewed | |
dc.identifier.fulltext | Fulltext https://www.duo.uio.no/bitstream/handle/10852/50087/1/13059_2016_Article_923.pdf | |
dc.type.version | PublishedVersion | |
cristin.articleid | 54 | |