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PHi-C2: interpreting Hi-C data as the dynamic 3D genome state
SUMMARY: High-throughput chromosome conformation capture (Hi-C) is a widely used assay for studying the three-dimensional (3D) genome organization across the whole genome. Here, we present PHi-C2, a Python package supported by mathematical and biophysical polymer modeling that converts input Hi-C ma...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9620818/ https://www.ncbi.nlm.nih.gov/pubmed/36087002 http://dx.doi.org/10.1093/bioinformatics/btac613 |
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author | Shinkai, Soya Itoga, Hiroya Kyoda, Koji Onami, Shuichi |
author_facet | Shinkai, Soya Itoga, Hiroya Kyoda, Koji Onami, Shuichi |
author_sort | Shinkai, Soya |
collection | PubMed |
description | SUMMARY: High-throughput chromosome conformation capture (Hi-C) is a widely used assay for studying the three-dimensional (3D) genome organization across the whole genome. Here, we present PHi-C2, a Python package supported by mathematical and biophysical polymer modeling that converts input Hi-C matrix data into the polymer model’s dynamics, structural conformations and rheological features. The updated optimization algorithm for regenerating a highly similar Hi-C matrix provides a fast and accurate optimal solution compared to the previous version by eliminating the factors underlying the inefficiency of the optimization algorithm in the iterative optimization process. In addition, we have enabled a Google Colab workflow to run the algorithm, wherein users can easily change the parameters and check the results in the notebook. Overall, PHi-C2 represents a valuable tool for mining the dynamic 3D genome state embedded in Hi-C data. AVAILABILITY AND IMPLEMENTATION: PHi-C2 as the phic Python package is freely available under the GPL license and can be installed from the Python package index. The source code is available from GitHub at https://github.com/soyashinkai/PHi-C2. Moreover, users do not have to prepare a Python environment because PHi-C2 can run on Google Colab (https://bit.ly/3rlptGI). SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. |
format | Online Article Text |
id | pubmed-9620818 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-96208182022-11-01 PHi-C2: interpreting Hi-C data as the dynamic 3D genome state Shinkai, Soya Itoga, Hiroya Kyoda, Koji Onami, Shuichi Bioinformatics Applications Notes SUMMARY: High-throughput chromosome conformation capture (Hi-C) is a widely used assay for studying the three-dimensional (3D) genome organization across the whole genome. Here, we present PHi-C2, a Python package supported by mathematical and biophysical polymer modeling that converts input Hi-C matrix data into the polymer model’s dynamics, structural conformations and rheological features. The updated optimization algorithm for regenerating a highly similar Hi-C matrix provides a fast and accurate optimal solution compared to the previous version by eliminating the factors underlying the inefficiency of the optimization algorithm in the iterative optimization process. In addition, we have enabled a Google Colab workflow to run the algorithm, wherein users can easily change the parameters and check the results in the notebook. Overall, PHi-C2 represents a valuable tool for mining the dynamic 3D genome state embedded in Hi-C data. AVAILABILITY AND IMPLEMENTATION: PHi-C2 as the phic Python package is freely available under the GPL license and can be installed from the Python package index. The source code is available from GitHub at https://github.com/soyashinkai/PHi-C2. Moreover, users do not have to prepare a Python environment because PHi-C2 can run on Google Colab (https://bit.ly/3rlptGI). SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2022-09-10 /pmc/articles/PMC9620818/ /pubmed/36087002 http://dx.doi.org/10.1093/bioinformatics/btac613 Text en © The Author(s) 2022. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Applications Notes Shinkai, Soya Itoga, Hiroya Kyoda, Koji Onami, Shuichi PHi-C2: interpreting Hi-C data as the dynamic 3D genome state |
title | PHi-C2: interpreting Hi-C data as the dynamic 3D genome state |
title_full | PHi-C2: interpreting Hi-C data as the dynamic 3D genome state |
title_fullStr | PHi-C2: interpreting Hi-C data as the dynamic 3D genome state |
title_full_unstemmed | PHi-C2: interpreting Hi-C data as the dynamic 3D genome state |
title_short | PHi-C2: interpreting Hi-C data as the dynamic 3D genome state |
title_sort | phi-c2: interpreting hi-c data as the dynamic 3d genome state |
topic | Applications Notes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9620818/ https://www.ncbi.nlm.nih.gov/pubmed/36087002 http://dx.doi.org/10.1093/bioinformatics/btac613 |
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