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Mapping robust multiscale communities in chromosome contact networks
To better understand DNA’s 3D folding in cell nuclei, researchers developed chromosome capture methods such as Hi-C that measure the contact frequencies between all DNA segment pairs across the genome. As Hi-C data sets often are massive, it is common to use bioinformatics methods to group DNA segme...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10415398/ https://www.ncbi.nlm.nih.gov/pubmed/37563218 http://dx.doi.org/10.1038/s41598-023-39522-7 |
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author | Holmgren, Anton Bernenko, Dolores Lizana, Ludvig |
author_facet | Holmgren, Anton Bernenko, Dolores Lizana, Ludvig |
author_sort | Holmgren, Anton |
collection | PubMed |
description | To better understand DNA’s 3D folding in cell nuclei, researchers developed chromosome capture methods such as Hi-C that measure the contact frequencies between all DNA segment pairs across the genome. As Hi-C data sets often are massive, it is common to use bioinformatics methods to group DNA segments into 3D regions with correlated contact patterns, such as Topologically associated domains and A/B compartments. Recently, another research direction emerged that treats the Hi-C data as a network of 3D contacts. In this representation, one can use community detection algorithms from complex network theory that group nodes into tightly connected mesoscale communities. However, because Hi-C networks are so densely connected, several node partitions may represent feasible solutions to the community detection problem but are indistinguishable unless including other data. Because this limitation is a fundamental property of the network, this problem persists regardless of the community-finding or data-clustering method. To help remedy this problem, we developed a method that charts the solution landscape of network partitions in Hi-C data from human cells. Our approach allows us to scan seamlessly through the scales of the network and determine regimes where we can expect reliable community structures. We find that some scales are more robust than others and that strong clusters may differ significantly. Our work highlights that finding a robust community structure hinges on thoughtful algorithm design or method cross-evaluation. |
format | Online Article Text |
id | pubmed-10415398 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-104153982023-08-12 Mapping robust multiscale communities in chromosome contact networks Holmgren, Anton Bernenko, Dolores Lizana, Ludvig Sci Rep Article To better understand DNA’s 3D folding in cell nuclei, researchers developed chromosome capture methods such as Hi-C that measure the contact frequencies between all DNA segment pairs across the genome. As Hi-C data sets often are massive, it is common to use bioinformatics methods to group DNA segments into 3D regions with correlated contact patterns, such as Topologically associated domains and A/B compartments. Recently, another research direction emerged that treats the Hi-C data as a network of 3D contacts. In this representation, one can use community detection algorithms from complex network theory that group nodes into tightly connected mesoscale communities. However, because Hi-C networks are so densely connected, several node partitions may represent feasible solutions to the community detection problem but are indistinguishable unless including other data. Because this limitation is a fundamental property of the network, this problem persists regardless of the community-finding or data-clustering method. To help remedy this problem, we developed a method that charts the solution landscape of network partitions in Hi-C data from human cells. Our approach allows us to scan seamlessly through the scales of the network and determine regimes where we can expect reliable community structures. We find that some scales are more robust than others and that strong clusters may differ significantly. Our work highlights that finding a robust community structure hinges on thoughtful algorithm design or method cross-evaluation. Nature Publishing Group UK 2023-08-10 /pmc/articles/PMC10415398/ /pubmed/37563218 http://dx.doi.org/10.1038/s41598-023-39522-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Holmgren, Anton Bernenko, Dolores Lizana, Ludvig Mapping robust multiscale communities in chromosome contact networks |
title | Mapping robust multiscale communities in chromosome contact networks |
title_full | Mapping robust multiscale communities in chromosome contact networks |
title_fullStr | Mapping robust multiscale communities in chromosome contact networks |
title_full_unstemmed | Mapping robust multiscale communities in chromosome contact networks |
title_short | Mapping robust multiscale communities in chromosome contact networks |
title_sort | mapping robust multiscale communities in chromosome contact networks |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10415398/ https://www.ncbi.nlm.nih.gov/pubmed/37563218 http://dx.doi.org/10.1038/s41598-023-39522-7 |
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