Learning the distribution of single-cell chromosome conformations in bacteria reveals emergent order across genomic scales

The order and variability of bacterial chromosome organization, contained within the distribution of chromosome conformations, are unclear. Here, the authors develop a fully data-driven maximum entropy approach to extract single-cell 3D chromosome conformations from Hi-C experiments on the model org...

Description complète

Enregistré dans:
Détails bibliographiques
Auteurs principaux: Joris J. B. Messelink, Muriel C. F. van Teeseling, Jacqueline Janssen, Martin Thanbichler, Chase P. Broedersz
Format: article
Langue:EN
Publié: Nature Portfolio 2021
Sujets:
Q
Accès en ligne:https://doaj.org/article/84d87ae148d5440b8d200074a9cfa90f
Tags: Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
id oai:doaj.org-article:84d87ae148d5440b8d200074a9cfa90f
record_format dspace
spelling oai:doaj.org-article:84d87ae148d5440b8d200074a9cfa90f2021-12-02T14:23:03ZLearning the distribution of single-cell chromosome conformations in bacteria reveals emergent order across genomic scales10.1038/s41467-021-22189-x2041-1723https://doaj.org/article/84d87ae148d5440b8d200074a9cfa90f2021-03-01T00:00:00Zhttps://doi.org/10.1038/s41467-021-22189-xhttps://doaj.org/toc/2041-1723The order and variability of bacterial chromosome organization, contained within the distribution of chromosome conformations, are unclear. Here, the authors develop a fully data-driven maximum entropy approach to extract single-cell 3D chromosome conformations from Hi-C experiments on the model organism Caulobacter crescentus.Joris J. B. MesselinkMuriel C. F. van TeeselingJacqueline JanssenMartin ThanbichlerChase P. BroederszNature PortfolioarticleScienceQENNature Communications, Vol 12, Iss 1, Pp 1-9 (2021)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Joris J. B. Messelink
Muriel C. F. van Teeseling
Jacqueline Janssen
Martin Thanbichler
Chase P. Broedersz
Learning the distribution of single-cell chromosome conformations in bacteria reveals emergent order across genomic scales
description The order and variability of bacterial chromosome organization, contained within the distribution of chromosome conformations, are unclear. Here, the authors develop a fully data-driven maximum entropy approach to extract single-cell 3D chromosome conformations from Hi-C experiments on the model organism Caulobacter crescentus.
format article
author Joris J. B. Messelink
Muriel C. F. van Teeseling
Jacqueline Janssen
Martin Thanbichler
Chase P. Broedersz
author_facet Joris J. B. Messelink
Muriel C. F. van Teeseling
Jacqueline Janssen
Martin Thanbichler
Chase P. Broedersz
author_sort Joris J. B. Messelink
title Learning the distribution of single-cell chromosome conformations in bacteria reveals emergent order across genomic scales
title_short Learning the distribution of single-cell chromosome conformations in bacteria reveals emergent order across genomic scales
title_full Learning the distribution of single-cell chromosome conformations in bacteria reveals emergent order across genomic scales
title_fullStr Learning the distribution of single-cell chromosome conformations in bacteria reveals emergent order across genomic scales
title_full_unstemmed Learning the distribution of single-cell chromosome conformations in bacteria reveals emergent order across genomic scales
title_sort learning the distribution of single-cell chromosome conformations in bacteria reveals emergent order across genomic scales
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/84d87ae148d5440b8d200074a9cfa90f
work_keys_str_mv AT jorisjbmesselink learningthedistributionofsinglecellchromosomeconformationsinbacteriarevealsemergentorderacrossgenomicscales
AT murielcfvanteeseling learningthedistributionofsinglecellchromosomeconformationsinbacteriarevealsemergentorderacrossgenomicscales
AT jacquelinejanssen learningthedistributionofsinglecellchromosomeconformationsinbacteriarevealsemergentorderacrossgenomicscales
AT martinthanbichler learningthedistributionofsinglecellchromosomeconformationsinbacteriarevealsemergentorderacrossgenomicscales
AT chasepbroedersz learningthedistributionofsinglecellchromosomeconformationsinbacteriarevealsemergentorderacrossgenomicscales
_version_ 1718391497439576064