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Deep neural networks for human microRNA precursor detection

BACKGROUND: MicroRNAs (miRNAs) play important roles in a variety of biological processes by regulating gene expression at the post-transcriptional level. So, the discovery of new miRNAs has become a popular task in biological research. Since the experimental identification of miRNAs is time-consumin...

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Autores principales: Zheng, Xueming, Fu, Xingli, Wang, Kaicheng, Wang, Meng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6958766/
https://www.ncbi.nlm.nih.gov/pubmed/31931701
http://dx.doi.org/10.1186/s12859-020-3339-7
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author Zheng, Xueming
Fu, Xingli
Wang, Kaicheng
Wang, Meng
author_facet Zheng, Xueming
Fu, Xingli
Wang, Kaicheng
Wang, Meng
author_sort Zheng, Xueming
collection PubMed
description BACKGROUND: MicroRNAs (miRNAs) play important roles in a variety of biological processes by regulating gene expression at the post-transcriptional level. So, the discovery of new miRNAs has become a popular task in biological research. Since the experimental identification of miRNAs is time-consuming, many computational tools have been developed to identify miRNA precursor (pre-miRNA). Most of these computation methods are based on traditional machine learning methods and their performance depends heavily on the selected features which are usually determined by domain experts. To develop easily implemented methods with better performance, we investigated different deep learning architectures for the pre-miRNAs identification. RESULTS: In this work, we applied convolution neural networks (CNN) and recurrent neural networks (RNN) to predict human pre-miRNAs. We combined the sequences with the predicted secondary structures of pre-miRNAs as input features of our models, avoiding the feature extraction and selection process by hand. The models were easily trained on the training dataset with low generalization error, and therefore had satisfactory performance on the test dataset. The prediction results on the same benchmark dataset showed that our models outperformed or were highly comparable to other state-of-the-art methods in this area. Furthermore, our CNN model trained on human dataset had high prediction accuracy on data from other species. CONCLUSIONS: Deep neural networks (DNN) could be utilized for the human pre-miRNAs detection with high performance. Complex features of RNA sequences could be automatically extracted by CNN and RNN, which were used for the pre-miRNAs prediction. Through proper regularization, our deep learning models, although trained on comparatively small dataset, had strong generalization ability.
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spelling pubmed-69587662020-01-17 Deep neural networks for human microRNA precursor detection Zheng, Xueming Fu, Xingli Wang, Kaicheng Wang, Meng BMC Bioinformatics Methodology Article BACKGROUND: MicroRNAs (miRNAs) play important roles in a variety of biological processes by regulating gene expression at the post-transcriptional level. So, the discovery of new miRNAs has become a popular task in biological research. Since the experimental identification of miRNAs is time-consuming, many computational tools have been developed to identify miRNA precursor (pre-miRNA). Most of these computation methods are based on traditional machine learning methods and their performance depends heavily on the selected features which are usually determined by domain experts. To develop easily implemented methods with better performance, we investigated different deep learning architectures for the pre-miRNAs identification. RESULTS: In this work, we applied convolution neural networks (CNN) and recurrent neural networks (RNN) to predict human pre-miRNAs. We combined the sequences with the predicted secondary structures of pre-miRNAs as input features of our models, avoiding the feature extraction and selection process by hand. The models were easily trained on the training dataset with low generalization error, and therefore had satisfactory performance on the test dataset. The prediction results on the same benchmark dataset showed that our models outperformed or were highly comparable to other state-of-the-art methods in this area. Furthermore, our CNN model trained on human dataset had high prediction accuracy on data from other species. CONCLUSIONS: Deep neural networks (DNN) could be utilized for the human pre-miRNAs detection with high performance. Complex features of RNA sequences could be automatically extracted by CNN and RNN, which were used for the pre-miRNAs prediction. Through proper regularization, our deep learning models, although trained on comparatively small dataset, had strong generalization ability. BioMed Central 2020-01-13 /pmc/articles/PMC6958766/ /pubmed/31931701 http://dx.doi.org/10.1186/s12859-020-3339-7 Text en © The Author(s). 2020 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.
spellingShingle Methodology Article
Zheng, Xueming
Fu, Xingli
Wang, Kaicheng
Wang, Meng
Deep neural networks for human microRNA precursor detection
title Deep neural networks for human microRNA precursor detection
title_full Deep neural networks for human microRNA precursor detection
title_fullStr Deep neural networks for human microRNA precursor detection
title_full_unstemmed Deep neural networks for human microRNA precursor detection
title_short Deep neural networks for human microRNA precursor detection
title_sort deep neural networks for human microrna precursor detection
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6958766/
https://www.ncbi.nlm.nih.gov/pubmed/31931701
http://dx.doi.org/10.1186/s12859-020-3339-7
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