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Heterogeneous Graph Convolutional Networks and Matrix Completion for miRNA-Disease Association Prediction

Due to the cost and complexity of biological experiments, many computational methods have been proposed to predict potential miRNA-disease associations by utilizing known miRNA-disease associations and other related information. However, there are some challenges for these computational methods. Fir...

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Autores principales: Zhu, Rongxiang, Ji, Chaojie, Wang, Yingying, Cai, Yunpeng, Wu, Hongyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7468400/
https://www.ncbi.nlm.nih.gov/pubmed/32974293
http://dx.doi.org/10.3389/fbioe.2020.00901
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author Zhu, Rongxiang
Ji, Chaojie
Wang, Yingying
Cai, Yunpeng
Wu, Hongyan
author_facet Zhu, Rongxiang
Ji, Chaojie
Wang, Yingying
Cai, Yunpeng
Wu, Hongyan
author_sort Zhu, Rongxiang
collection PubMed
description Due to the cost and complexity of biological experiments, many computational methods have been proposed to predict potential miRNA-disease associations by utilizing known miRNA-disease associations and other related information. However, there are some challenges for these computational methods. First, the relationships between miRNAs and diseases are complex. The computational network should consider the local and global influence of neighborhoods from the network. Furthermore, predicting disease-related miRNAs without any known associations is also very important. This study presents a new computational method that constructs a heterogeneous network composed of a miRNA similarity network, disease similarity network, and known miRNA-disease association network. The miRNA similarity considers the miRNAs and their possible families and clusters. The information of each node in heterogeneous network is obtained by aggregating neighborhood information with graph convolutional networks (GCNs), which can pass the information of a node to its intermediate and distant neighbors. Disease-related miRNAs with no known associations can be predicted with the reconstructed heterogeneous matrix. We apply 5-fold cross-validation, leave-one-disease-out cross-validation, and global and local leave-one-out cross-validation to evaluate our method. The corresponding areas under the curves (AUCs) are 0.9616, 0.9946, 0.9656, and 0.9532, confirming that our approach significantly outperforms the state-of-the-art methods. Case studies show that this approach can effectively predict new diseases without any known miRNAs.
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spelling pubmed-74684002020-09-23 Heterogeneous Graph Convolutional Networks and Matrix Completion for miRNA-Disease Association Prediction Zhu, Rongxiang Ji, Chaojie Wang, Yingying Cai, Yunpeng Wu, Hongyan Front Bioeng Biotechnol Bioengineering and Biotechnology Due to the cost and complexity of biological experiments, many computational methods have been proposed to predict potential miRNA-disease associations by utilizing known miRNA-disease associations and other related information. However, there are some challenges for these computational methods. First, the relationships between miRNAs and diseases are complex. The computational network should consider the local and global influence of neighborhoods from the network. Furthermore, predicting disease-related miRNAs without any known associations is also very important. This study presents a new computational method that constructs a heterogeneous network composed of a miRNA similarity network, disease similarity network, and known miRNA-disease association network. The miRNA similarity considers the miRNAs and their possible families and clusters. The information of each node in heterogeneous network is obtained by aggregating neighborhood information with graph convolutional networks (GCNs), which can pass the information of a node to its intermediate and distant neighbors. Disease-related miRNAs with no known associations can be predicted with the reconstructed heterogeneous matrix. We apply 5-fold cross-validation, leave-one-disease-out cross-validation, and global and local leave-one-out cross-validation to evaluate our method. The corresponding areas under the curves (AUCs) are 0.9616, 0.9946, 0.9656, and 0.9532, confirming that our approach significantly outperforms the state-of-the-art methods. Case studies show that this approach can effectively predict new diseases without any known miRNAs. Frontiers Media S.A. 2020-08-20 /pmc/articles/PMC7468400/ /pubmed/32974293 http://dx.doi.org/10.3389/fbioe.2020.00901 Text en Copyright © 2020 Zhu, Ji, Wang, Cai and Wu. 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 Bioengineering and Biotechnology
Zhu, Rongxiang
Ji, Chaojie
Wang, Yingying
Cai, Yunpeng
Wu, Hongyan
Heterogeneous Graph Convolutional Networks and Matrix Completion for miRNA-Disease Association Prediction
title Heterogeneous Graph Convolutional Networks and Matrix Completion for miRNA-Disease Association Prediction
title_full Heterogeneous Graph Convolutional Networks and Matrix Completion for miRNA-Disease Association Prediction
title_fullStr Heterogeneous Graph Convolutional Networks and Matrix Completion for miRNA-Disease Association Prediction
title_full_unstemmed Heterogeneous Graph Convolutional Networks and Matrix Completion for miRNA-Disease Association Prediction
title_short Heterogeneous Graph Convolutional Networks and Matrix Completion for miRNA-Disease Association Prediction
title_sort heterogeneous graph convolutional networks and matrix completion for mirna-disease association prediction
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7468400/
https://www.ncbi.nlm.nih.gov/pubmed/32974293
http://dx.doi.org/10.3389/fbioe.2020.00901
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