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Pattern recognition of topologically associating domains using deep learning

BACKGROUND: Recent increasing evidence indicates that three-dimensional chromosome structure plays an important role in genomic function. Topologically associating domains (TADs) are self-interacting regions that have been shown to be a chromosomal structural unit. During evolution, these are conser...

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Autores principales: Yang, Jhen Yuan, Chang, Jia-Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9732975/
https://www.ncbi.nlm.nih.gov/pubmed/36482308
http://dx.doi.org/10.1186/s12859-022-05075-1
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author Yang, Jhen Yuan
Chang, Jia-Ming
author_facet Yang, Jhen Yuan
Chang, Jia-Ming
author_sort Yang, Jhen Yuan
collection PubMed
description BACKGROUND: Recent increasing evidence indicates that three-dimensional chromosome structure plays an important role in genomic function. Topologically associating domains (TADs) are self-interacting regions that have been shown to be a chromosomal structural unit. During evolution, these are conserved based on checking synteny block cross species. Are there common TAD patterns across species or cell lines? RESULTS: To address the above question, we propose a novel task—TAD recognition—as opposed to traditional TAD identification. Specifically, we treat Hi-C maps as images, thus re-casting TAD recognition as image pattern recognition, for which we use a convolutional neural network and a residual neural network. In addition, we propose an elegant way to generate non-TAD data for binary classification. We demonstrate deep learning performance which is quite promising, AUC > 0.80, through cross-species and cell-type validation. CONCLUSIONS: TADs have been shown to be conserved during evolution. Interestingly, our results confirm that the TAD recognition model is practical across species, which indicates that TADs between human and mouse show common patterns from an image classification point of view. Our approach could be a new way to identify TAD variations or patterns among Hi-C maps. For example, TADs of two Hi-C maps are conserved if the two classification models are exchangeable. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-022-05075-1.
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spelling pubmed-97329752022-12-10 Pattern recognition of topologically associating domains using deep learning Yang, Jhen Yuan Chang, Jia-Ming BMC Bioinformatics Research BACKGROUND: Recent increasing evidence indicates that three-dimensional chromosome structure plays an important role in genomic function. Topologically associating domains (TADs) are self-interacting regions that have been shown to be a chromosomal structural unit. During evolution, these are conserved based on checking synteny block cross species. Are there common TAD patterns across species or cell lines? RESULTS: To address the above question, we propose a novel task—TAD recognition—as opposed to traditional TAD identification. Specifically, we treat Hi-C maps as images, thus re-casting TAD recognition as image pattern recognition, for which we use a convolutional neural network and a residual neural network. In addition, we propose an elegant way to generate non-TAD data for binary classification. We demonstrate deep learning performance which is quite promising, AUC > 0.80, through cross-species and cell-type validation. CONCLUSIONS: TADs have been shown to be conserved during evolution. Interestingly, our results confirm that the TAD recognition model is practical across species, which indicates that TADs between human and mouse show common patterns from an image classification point of view. Our approach could be a new way to identify TAD variations or patterns among Hi-C maps. For example, TADs of two Hi-C maps are conserved if the two classification models are exchangeable. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-022-05075-1. BioMed Central 2022-12-08 /pmc/articles/PMC9732975/ /pubmed/36482308 http://dx.doi.org/10.1186/s12859-022-05075-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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 Research
Yang, Jhen Yuan
Chang, Jia-Ming
Pattern recognition of topologically associating domains using deep learning
title Pattern recognition of topologically associating domains using deep learning
title_full Pattern recognition of topologically associating domains using deep learning
title_fullStr Pattern recognition of topologically associating domains using deep learning
title_full_unstemmed Pattern recognition of topologically associating domains using deep learning
title_short Pattern recognition of topologically associating domains using deep learning
title_sort pattern recognition of topologically associating domains using deep learning
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9732975/
https://www.ncbi.nlm.nih.gov/pubmed/36482308
http://dx.doi.org/10.1186/s12859-022-05075-1
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