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HiCHap: a package to correct and analyze the diploid Hi-C data
BACKGROUND: In diploid cells, it is important to construct maternal and paternal Hi-C contact maps respectively since the two homologous chromosomes can differ in chromatin three-dimensional (3D) organization. Though previous softwares could construct diploid (maternal and paternal) Hi-C contact map...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7590616/ https://www.ncbi.nlm.nih.gov/pubmed/33109075 http://dx.doi.org/10.1186/s12864-020-07165-x |
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author | Luo, Han Li, Xinxin Fu, Haitao Peng, Cheng |
author_facet | Luo, Han Li, Xinxin Fu, Haitao Peng, Cheng |
author_sort | Luo, Han |
collection | PubMed |
description | BACKGROUND: In diploid cells, it is important to construct maternal and paternal Hi-C contact maps respectively since the two homologous chromosomes can differ in chromatin three-dimensional (3D) organization. Though previous softwares could construct diploid (maternal and paternal) Hi-C contact maps by using phased genetic variants, they all neglected the systematic biases in diploid Hi-C contact maps caused by variable genetic variant density in the genome. In addition, few of softwares provided quantitative analyses on allele-specific chromatin 3D organization, including compartment, topological domain and chromatin loop. RESULTS: In this work, we revealed the feature of allele-assignment bias caused by the variable genetic variant density, and then proposed a novel strategy to correct the systematic biases in diploid Hi-C contact maps. Based on the bias correction, we developed an integrated tool, called HiCHap, to perform read mapping, contact map construction, whole-genome identification of compartments, topological domains and chromatin loops, and allele-specific testing for diploid Hi-C data. Our results show that the correction on allele-assignment bias in HiCHap does significantly improve the quality of diploid Hi-C contact maps, which subsequently facilitates the whole-genome identification of diploid chromatin 3D organization, including compartments, topological domains and chromatin loops. Finally, HiCHap also supports the data analysis for haploid Hi-C maps without distinguishing two homologous chromosomes. CONCLUSIONS: We provided an integrated package HiCHap to perform the data processing, bias correction and structural analysis for diploid Hi-C data. The source code and tutorial of software HiCHap are freely available at https://pypi.org/project/HiCHap/. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-020-07165-x. |
format | Online Article Text |
id | pubmed-7590616 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-75906162020-10-27 HiCHap: a package to correct and analyze the diploid Hi-C data Luo, Han Li, Xinxin Fu, Haitao Peng, Cheng BMC Genomics Software BACKGROUND: In diploid cells, it is important to construct maternal and paternal Hi-C contact maps respectively since the two homologous chromosomes can differ in chromatin three-dimensional (3D) organization. Though previous softwares could construct diploid (maternal and paternal) Hi-C contact maps by using phased genetic variants, they all neglected the systematic biases in diploid Hi-C contact maps caused by variable genetic variant density in the genome. In addition, few of softwares provided quantitative analyses on allele-specific chromatin 3D organization, including compartment, topological domain and chromatin loop. RESULTS: In this work, we revealed the feature of allele-assignment bias caused by the variable genetic variant density, and then proposed a novel strategy to correct the systematic biases in diploid Hi-C contact maps. Based on the bias correction, we developed an integrated tool, called HiCHap, to perform read mapping, contact map construction, whole-genome identification of compartments, topological domains and chromatin loops, and allele-specific testing for diploid Hi-C data. Our results show that the correction on allele-assignment bias in HiCHap does significantly improve the quality of diploid Hi-C contact maps, which subsequently facilitates the whole-genome identification of diploid chromatin 3D organization, including compartments, topological domains and chromatin loops. Finally, HiCHap also supports the data analysis for haploid Hi-C maps without distinguishing two homologous chromosomes. CONCLUSIONS: We provided an integrated package HiCHap to perform the data processing, bias correction and structural analysis for diploid Hi-C data. The source code and tutorial of software HiCHap are freely available at https://pypi.org/project/HiCHap/. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-020-07165-x. BioMed Central 2020-10-27 /pmc/articles/PMC7590616/ /pubmed/33109075 http://dx.doi.org/10.1186/s12864-020-07165-x Text en © The Author(s) 2020 Open AccessThis 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Software Luo, Han Li, Xinxin Fu, Haitao Peng, Cheng HiCHap: a package to correct and analyze the diploid Hi-C data |
title | HiCHap: a package to correct and analyze the diploid Hi-C data |
title_full | HiCHap: a package to correct and analyze the diploid Hi-C data |
title_fullStr | HiCHap: a package to correct and analyze the diploid Hi-C data |
title_full_unstemmed | HiCHap: a package to correct and analyze the diploid Hi-C data |
title_short | HiCHap: a package to correct and analyze the diploid Hi-C data |
title_sort | hichap: a package to correct and analyze the diploid hi-c data |
topic | Software |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7590616/ https://www.ncbi.nlm.nih.gov/pubmed/33109075 http://dx.doi.org/10.1186/s12864-020-07165-x |
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