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Non-backtracking walks reveal compartments in sparse chromatin interaction networks
Chromatin communities stabilized by protein machinery play essential role in gene regulation and refine global polymeric folding of the chromatin fiber. However, treatment of these communities in the framework of the classical network theory (stochastic block model, SBM) does not take into account i...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7347895/ https://www.ncbi.nlm.nih.gov/pubmed/32647272 http://dx.doi.org/10.1038/s41598-020-68182-0 |
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author | Polovnikov, K. Gorsky, A. Nechaev, S. Razin, S. V. Ulianov, S. V. |
author_facet | Polovnikov, K. Gorsky, A. Nechaev, S. Razin, S. V. Ulianov, S. V. |
author_sort | Polovnikov, K. |
collection | PubMed |
description | Chromatin communities stabilized by protein machinery play essential role in gene regulation and refine global polymeric folding of the chromatin fiber. However, treatment of these communities in the framework of the classical network theory (stochastic block model, SBM) does not take into account intrinsic linear connectivity of the chromatin loci. Here we propose the polymer block model, paving the way for community detection in polymer networks. On the basis of this new model we modify the non-backtracking flow operator and suggest the first protocol for annotation of compartmental domains in sparse single cell Hi-C matrices. In particular, we prove that our approach corresponds to the maximum entropy principle. The benchmark analyses demonstrates that the spectrum of the polymer non-backtracking operator resolves the true compartmental structure up to the theoretical detectability threshold, while all commonly used operators fail above it. We test various operators on real data and conclude that the sizes of the non-backtracking single cell domains are most close to the sizes of compartments from the population data. Moreover, the found domains clearly segregate in the gene density and correlate with the population compartmental mask, corroborating biological significance of our annotation of the chromatin compartmental domains in single cells Hi-C matrices. |
format | Online Article Text |
id | pubmed-7347895 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73478952020-07-14 Non-backtracking walks reveal compartments in sparse chromatin interaction networks Polovnikov, K. Gorsky, A. Nechaev, S. Razin, S. V. Ulianov, S. V. Sci Rep Article Chromatin communities stabilized by protein machinery play essential role in gene regulation and refine global polymeric folding of the chromatin fiber. However, treatment of these communities in the framework of the classical network theory (stochastic block model, SBM) does not take into account intrinsic linear connectivity of the chromatin loci. Here we propose the polymer block model, paving the way for community detection in polymer networks. On the basis of this new model we modify the non-backtracking flow operator and suggest the first protocol for annotation of compartmental domains in sparse single cell Hi-C matrices. In particular, we prove that our approach corresponds to the maximum entropy principle. The benchmark analyses demonstrates that the spectrum of the polymer non-backtracking operator resolves the true compartmental structure up to the theoretical detectability threshold, while all commonly used operators fail above it. We test various operators on real data and conclude that the sizes of the non-backtracking single cell domains are most close to the sizes of compartments from the population data. Moreover, the found domains clearly segregate in the gene density and correlate with the population compartmental mask, corroborating biological significance of our annotation of the chromatin compartmental domains in single cells Hi-C matrices. Nature Publishing Group UK 2020-07-09 /pmc/articles/PMC7347895/ /pubmed/32647272 http://dx.doi.org/10.1038/s41598-020-68182-0 Text en © The Author(s) 2020 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Polovnikov, K. Gorsky, A. Nechaev, S. Razin, S. V. Ulianov, S. V. Non-backtracking walks reveal compartments in sparse chromatin interaction networks |
title | Non-backtracking walks reveal compartments in sparse chromatin interaction networks |
title_full | Non-backtracking walks reveal compartments in sparse chromatin interaction networks |
title_fullStr | Non-backtracking walks reveal compartments in sparse chromatin interaction networks |
title_full_unstemmed | Non-backtracking walks reveal compartments in sparse chromatin interaction networks |
title_short | Non-backtracking walks reveal compartments in sparse chromatin interaction networks |
title_sort | non-backtracking walks reveal compartments in sparse chromatin interaction networks |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7347895/ https://www.ncbi.nlm.nih.gov/pubmed/32647272 http://dx.doi.org/10.1038/s41598-020-68182-0 |
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