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A Deep Neural Network for Identifying DNA N4-Methylcytosine Sites
Motivation: N4-methylcytosine (4mC) plays an important role in host defense and transcriptional regulation. Accurate identification of 4mc sites provides a more comprehensive understanding of its biological effects. At present, the traditional machine learning algorithms are used in the research on...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7067889/ https://www.ncbi.nlm.nih.gov/pubmed/32211035 http://dx.doi.org/10.3389/fgene.2020.00209 |
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author | Zeng, Feng Fang, Guanyun Yao, Lan |
author_facet | Zeng, Feng Fang, Guanyun Yao, Lan |
author_sort | Zeng, Feng |
collection | PubMed |
description | Motivation: N4-methylcytosine (4mC) plays an important role in host defense and transcriptional regulation. Accurate identification of 4mc sites provides a more comprehensive understanding of its biological effects. At present, the traditional machine learning algorithms are used in the research on 4mC sites prediction, but the complexity of the algorithms is relatively high, which is not suitable for the processing of large data sets, and the accuracy of prediction needs to be improved. Therefore, it is necessary to develop a new and effective method to accurately identify 4mC sites. Results: In this work, we found a large number of 4mC sites and non 4mC sites of Caenorhabditis elegans (C. elegans) from the latest MethSMRT website, which greatly expanded the dataset of C. elegans, and developed a hybrid deep neural network framework named 4mcDeep-CBI, aiming to identify 4mC sites. In order to obtain the high latitude information of the feature, we input the preliminary extracted features into the Convolutional Neural Network (CNN) and Bidirectional Long Short Term Memory network (BLSTM) to generate advanced features. Taking the advanced features as algorithm input, we have proposed an integrated algorithm to improve feature representation. Experimental results on large new dataset show that the proposed predictor is able to achieve generally better performance in identifying 4mC sites as compared to the state-of-art predictor. Notably, this is the first study of identifying 4mC sites using deep neural network. Moreover, our model runs much faster than the state-of-art predictor. |
format | Online Article Text |
id | pubmed-7067889 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70678892020-03-24 A Deep Neural Network for Identifying DNA N4-Methylcytosine Sites Zeng, Feng Fang, Guanyun Yao, Lan Front Genet Genetics Motivation: N4-methylcytosine (4mC) plays an important role in host defense and transcriptional regulation. Accurate identification of 4mc sites provides a more comprehensive understanding of its biological effects. At present, the traditional machine learning algorithms are used in the research on 4mC sites prediction, but the complexity of the algorithms is relatively high, which is not suitable for the processing of large data sets, and the accuracy of prediction needs to be improved. Therefore, it is necessary to develop a new and effective method to accurately identify 4mC sites. Results: In this work, we found a large number of 4mC sites and non 4mC sites of Caenorhabditis elegans (C. elegans) from the latest MethSMRT website, which greatly expanded the dataset of C. elegans, and developed a hybrid deep neural network framework named 4mcDeep-CBI, aiming to identify 4mC sites. In order to obtain the high latitude information of the feature, we input the preliminary extracted features into the Convolutional Neural Network (CNN) and Bidirectional Long Short Term Memory network (BLSTM) to generate advanced features. Taking the advanced features as algorithm input, we have proposed an integrated algorithm to improve feature representation. Experimental results on large new dataset show that the proposed predictor is able to achieve generally better performance in identifying 4mC sites as compared to the state-of-art predictor. Notably, this is the first study of identifying 4mC sites using deep neural network. Moreover, our model runs much faster than the state-of-art predictor. Frontiers Media S.A. 2020-03-06 /pmc/articles/PMC7067889/ /pubmed/32211035 http://dx.doi.org/10.3389/fgene.2020.00209 Text en Copyright © 2020 Zeng, Fang and Yao. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Genetics Zeng, Feng Fang, Guanyun Yao, Lan A Deep Neural Network for Identifying DNA N4-Methylcytosine Sites |
title | A Deep Neural Network for Identifying DNA N4-Methylcytosine Sites |
title_full | A Deep Neural Network for Identifying DNA N4-Methylcytosine Sites |
title_fullStr | A Deep Neural Network for Identifying DNA N4-Methylcytosine Sites |
title_full_unstemmed | A Deep Neural Network for Identifying DNA N4-Methylcytosine Sites |
title_short | A Deep Neural Network for Identifying DNA N4-Methylcytosine Sites |
title_sort | deep neural network for identifying dna n4-methylcytosine sites |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7067889/ https://www.ncbi.nlm.nih.gov/pubmed/32211035 http://dx.doi.org/10.3389/fgene.2020.00209 |
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