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HiC1Dmetrics: framework to extract various one-dimensional features from chromosome structure data

Eukaryotic genomes are organized in a three-dimensional spatial structure. In this regard, the development of chromosome conformation capture methods has enabled studies of chromosome organization on a genomic scale. Hi-C, the high-throughput chromosome conformation capture method, can reveal a popu...

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Detalles Bibliográficos
Autores principales: Wang, Jiankang, Nakato, Ryuichiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8769930/
https://www.ncbi.nlm.nih.gov/pubmed/34850813
http://dx.doi.org/10.1093/bib/bbab509
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author Wang, Jiankang
Nakato, Ryuichiro
author_facet Wang, Jiankang
Nakato, Ryuichiro
author_sort Wang, Jiankang
collection PubMed
description Eukaryotic genomes are organized in a three-dimensional spatial structure. In this regard, the development of chromosome conformation capture methods has enabled studies of chromosome organization on a genomic scale. Hi-C, the high-throughput chromosome conformation capture method, can reveal a population-averaged, hierarchical chromatin structure. The typical Hi-C analysis uses a two-dimensional (2D) contact matrix that indicates contact frequencies between all possible genomic position pairs. Oftentimes, however, such a 2D matrix is not amenable to handling quantitative comparisons, visualizations and integrations across multiple datasets. Although several one-dimensional (1D) metrics have been proposed to depict structural information in Hi-C data, their effectiveness is still underappreciated. Here, we first review the currently available 1D metrics for individual Hi-C samples or two-sample comparisons and then discuss their validity and suitable analysis scenarios. We also propose several new 1D metrics to identify additional unique features of chromosome structures. We highlight that the 1D metrics are reproducible and robust for comparing and visualizing multiple Hi-C samples. Moreover, we show that 1D metrics can be easily combined with epigenome tracks to annotate chromatin states in greater details. We develop a new framework, called HiC1Dmetrics, to summarize all 1D metrics discussed in this study. HiC1Dmetrics is open-source (github.com/wangjk321/HiC1Dmetrics) and can be accessed from both command-line and web-based interfaces. Our tool constitutes a useful resource for the community of chromosome-organization researchers.
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spelling pubmed-87699302022-01-20 HiC1Dmetrics: framework to extract various one-dimensional features from chromosome structure data Wang, Jiankang Nakato, Ryuichiro Brief Bioinform Problem Solving Protocol Eukaryotic genomes are organized in a three-dimensional spatial structure. In this regard, the development of chromosome conformation capture methods has enabled studies of chromosome organization on a genomic scale. Hi-C, the high-throughput chromosome conformation capture method, can reveal a population-averaged, hierarchical chromatin structure. The typical Hi-C analysis uses a two-dimensional (2D) contact matrix that indicates contact frequencies between all possible genomic position pairs. Oftentimes, however, such a 2D matrix is not amenable to handling quantitative comparisons, visualizations and integrations across multiple datasets. Although several one-dimensional (1D) metrics have been proposed to depict structural information in Hi-C data, their effectiveness is still underappreciated. Here, we first review the currently available 1D metrics for individual Hi-C samples or two-sample comparisons and then discuss their validity and suitable analysis scenarios. We also propose several new 1D metrics to identify additional unique features of chromosome structures. We highlight that the 1D metrics are reproducible and robust for comparing and visualizing multiple Hi-C samples. Moreover, we show that 1D metrics can be easily combined with epigenome tracks to annotate chromatin states in greater details. We develop a new framework, called HiC1Dmetrics, to summarize all 1D metrics discussed in this study. HiC1Dmetrics is open-source (github.com/wangjk321/HiC1Dmetrics) and can be accessed from both command-line and web-based interfaces. Our tool constitutes a useful resource for the community of chromosome-organization researchers. Oxford University Press 2021-12-01 /pmc/articles/PMC8769930/ /pubmed/34850813 http://dx.doi.org/10.1093/bib/bbab509 Text en © The Author(s) 2021. Published by Oxford University Press. https://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 (https://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 Problem Solving Protocol
Wang, Jiankang
Nakato, Ryuichiro
HiC1Dmetrics: framework to extract various one-dimensional features from chromosome structure data
title HiC1Dmetrics: framework to extract various one-dimensional features from chromosome structure data
title_full HiC1Dmetrics: framework to extract various one-dimensional features from chromosome structure data
title_fullStr HiC1Dmetrics: framework to extract various one-dimensional features from chromosome structure data
title_full_unstemmed HiC1Dmetrics: framework to extract various one-dimensional features from chromosome structure data
title_short HiC1Dmetrics: framework to extract various one-dimensional features from chromosome structure data
title_sort hic1dmetrics: framework to extract various one-dimensional features from chromosome structure data
topic Problem Solving Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8769930/
https://www.ncbi.nlm.nih.gov/pubmed/34850813
http://dx.doi.org/10.1093/bib/bbab509
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