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DFHiC: a dilated full convolution model to enhance the resolution of Hi-C data
MOTIVATION: Hi-C technology has been the most widely used chromosome conformation capture (3C) experiment that measures the frequency of all paired interactions in the entire genome, which is a powerful tool for studying the 3D structure of the genome. The fineness of the constructed genome structur...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10166584/ https://www.ncbi.nlm.nih.gov/pubmed/37084258 http://dx.doi.org/10.1093/bioinformatics/btad211 |
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author | Wang, Bin Liu, Kun Li, Yaohang Wang, Jianxin |
author_facet | Wang, Bin Liu, Kun Li, Yaohang Wang, Jianxin |
author_sort | Wang, Bin |
collection | PubMed |
description | MOTIVATION: Hi-C technology has been the most widely used chromosome conformation capture (3C) experiment that measures the frequency of all paired interactions in the entire genome, which is a powerful tool for studying the 3D structure of the genome. The fineness of the constructed genome structure depends on the resolution of Hi-C data. However, due to the fact that high-resolution Hi-C data require deep sequencing and thus high experimental cost, most available Hi-C data are in low-resolution. Hence, it is essential to enhance the quality of Hi-C data by developing the effective computational methods. RESULTS: In this work, we propose a novel method, so-called DFHiC, which generates the high-resolution Hi-C matrix from the low-resolution Hi-C matrix in the framework of the dilated convolutional neural network. The dilated convolution is able to effectively explore the global patterns in the overall Hi-C matrix by taking advantage of the information of the Hi-C matrix in a way of the longer genomic distance. Consequently, DFHiC can improve the resolution of the Hi-C matrix reliably and accurately. More importantly, the super-resolution Hi-C data enhanced by DFHiC is more in line with the real high-resolution Hi-C data than those done by the other existing methods, in terms of both chromatin significant interactions and identifying topologically associating domains. AVAILABILITY AND IMPLEMENTATION: https://github.com/BinWangCSU/DFHiC. |
format | Online Article Text |
id | pubmed-10166584 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-101665842023-05-09 DFHiC: a dilated full convolution model to enhance the resolution of Hi-C data Wang, Bin Liu, Kun Li, Yaohang Wang, Jianxin Bioinformatics Original Paper MOTIVATION: Hi-C technology has been the most widely used chromosome conformation capture (3C) experiment that measures the frequency of all paired interactions in the entire genome, which is a powerful tool for studying the 3D structure of the genome. The fineness of the constructed genome structure depends on the resolution of Hi-C data. However, due to the fact that high-resolution Hi-C data require deep sequencing and thus high experimental cost, most available Hi-C data are in low-resolution. Hence, it is essential to enhance the quality of Hi-C data by developing the effective computational methods. RESULTS: In this work, we propose a novel method, so-called DFHiC, which generates the high-resolution Hi-C matrix from the low-resolution Hi-C matrix in the framework of the dilated convolutional neural network. The dilated convolution is able to effectively explore the global patterns in the overall Hi-C matrix by taking advantage of the information of the Hi-C matrix in a way of the longer genomic distance. Consequently, DFHiC can improve the resolution of the Hi-C matrix reliably and accurately. More importantly, the super-resolution Hi-C data enhanced by DFHiC is more in line with the real high-resolution Hi-C data than those done by the other existing methods, in terms of both chromatin significant interactions and identifying topologically associating domains. AVAILABILITY AND IMPLEMENTATION: https://github.com/BinWangCSU/DFHiC. Oxford University Press 2023-04-21 /pmc/articles/PMC10166584/ /pubmed/37084258 http://dx.doi.org/10.1093/bioinformatics/btad211 Text en © The Author(s) 2023. 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 | Original Paper Wang, Bin Liu, Kun Li, Yaohang Wang, Jianxin DFHiC: a dilated full convolution model to enhance the resolution of Hi-C data |
title | DFHiC: a dilated full convolution model to enhance the resolution of Hi-C data |
title_full | DFHiC: a dilated full convolution model to enhance the resolution of Hi-C data |
title_fullStr | DFHiC: a dilated full convolution model to enhance the resolution of Hi-C data |
title_full_unstemmed | DFHiC: a dilated full convolution model to enhance the resolution of Hi-C data |
title_short | DFHiC: a dilated full convolution model to enhance the resolution of Hi-C data |
title_sort | dfhic: a dilated full convolution model to enhance the resolution of hi-c data |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10166584/ https://www.ncbi.nlm.nih.gov/pubmed/37084258 http://dx.doi.org/10.1093/bioinformatics/btad211 |
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