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Using GARDEN-NET and ChAseR to explore human haematopoietic 3D chromatin interaction networks
We introduce an R package and a web-based visualization tool for the representation, analysis and integration of epigenomic data in the context of 3D chromatin interaction networks. GARDEN-NET allows for the projection of user-submitted genomic features on pre-loaded chromatin interaction networks,...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7192625/ https://www.ncbi.nlm.nih.gov/pubmed/32182345 http://dx.doi.org/10.1093/nar/gkaa159 |
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author | Madrid-Mencía, Miguel Raineri, Emanuele Cao, Tran Bich Ngoc Pancaldi, Vera |
author_facet | Madrid-Mencía, Miguel Raineri, Emanuele Cao, Tran Bich Ngoc Pancaldi, Vera |
author_sort | Madrid-Mencía, Miguel |
collection | PubMed |
description | We introduce an R package and a web-based visualization tool for the representation, analysis and integration of epigenomic data in the context of 3D chromatin interaction networks. GARDEN-NET allows for the projection of user-submitted genomic features on pre-loaded chromatin interaction networks, exploiting the functionalities of the ChAseR package to explore the features in combination with chromatin network topology properties. We demonstrate the approach using published epigenomic and chromatin structure datasets in haematopoietic cells, including a collection of gene expression, DNA methylation and histone modifications data in primary healthy myeloid cells from hundreds of individuals. These datasets allow us to test the robustness of chromatin assortativity, which highlights which epigenomic features, alone or in combination, are more strongly associated with 3D genome architecture. We find evidence for genomic regions with specific histone modifications, DNA methylation, and gene expression levels to be forming preferential contacts in 3D nuclear space, to a different extent depending on the cell type and lineage. Finally, we examine replication timing data and find it to be the genomic feature most strongly associated with overall 3D chromatin organization at multiple scales, consistent with previous results from the literature. |
format | Online Article Text |
id | pubmed-7192625 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-71926252020-05-06 Using GARDEN-NET and ChAseR to explore human haematopoietic 3D chromatin interaction networks Madrid-Mencía, Miguel Raineri, Emanuele Cao, Tran Bich Ngoc Pancaldi, Vera Nucleic Acids Res Computational Biology We introduce an R package and a web-based visualization tool for the representation, analysis and integration of epigenomic data in the context of 3D chromatin interaction networks. GARDEN-NET allows for the projection of user-submitted genomic features on pre-loaded chromatin interaction networks, exploiting the functionalities of the ChAseR package to explore the features in combination with chromatin network topology properties. We demonstrate the approach using published epigenomic and chromatin structure datasets in haematopoietic cells, including a collection of gene expression, DNA methylation and histone modifications data in primary healthy myeloid cells from hundreds of individuals. These datasets allow us to test the robustness of chromatin assortativity, which highlights which epigenomic features, alone or in combination, are more strongly associated with 3D genome architecture. We find evidence for genomic regions with specific histone modifications, DNA methylation, and gene expression levels to be forming preferential contacts in 3D nuclear space, to a different extent depending on the cell type and lineage. Finally, we examine replication timing data and find it to be the genomic feature most strongly associated with overall 3D chromatin organization at multiple scales, consistent with previous results from the literature. Oxford University Press 2020-05-07 2020-03-17 /pmc/articles/PMC7192625/ /pubmed/32182345 http://dx.doi.org/10.1093/nar/gkaa159 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Computational Biology Madrid-Mencía, Miguel Raineri, Emanuele Cao, Tran Bich Ngoc Pancaldi, Vera Using GARDEN-NET and ChAseR to explore human haematopoietic 3D chromatin interaction networks |
title | Using GARDEN-NET and ChAseR to explore human haematopoietic 3D chromatin interaction networks |
title_full | Using GARDEN-NET and ChAseR to explore human haematopoietic 3D chromatin interaction networks |
title_fullStr | Using GARDEN-NET and ChAseR to explore human haematopoietic 3D chromatin interaction networks |
title_full_unstemmed | Using GARDEN-NET and ChAseR to explore human haematopoietic 3D chromatin interaction networks |
title_short | Using GARDEN-NET and ChAseR to explore human haematopoietic 3D chromatin interaction networks |
title_sort | using garden-net and chaser to explore human haematopoietic 3d chromatin interaction networks |
topic | Computational Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7192625/ https://www.ncbi.nlm.nih.gov/pubmed/32182345 http://dx.doi.org/10.1093/nar/gkaa159 |
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