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Predicting miRNA-disease associations using a hybrid feature representation in the heterogeneous network

BACKGROUND: Studies have found that miRNAs play an important role in many biological activities involved in human diseases. Revealing the associations between miRNA and disease by biological experiments is time-consuming and expensive. The computational approaches provide a new alternative. However,...

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Detalles Bibliográficos
Autores principales: Liu, Minghui, Yang, Jingyi, Wang, Jiacheng, Deng, Lei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7579981/
https://www.ncbi.nlm.nih.gov/pubmed/33087118
http://dx.doi.org/10.1186/s12920-020-00783-0
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author Liu, Minghui
Yang, Jingyi
Wang, Jiacheng
Deng, Lei
author_facet Liu, Minghui
Yang, Jingyi
Wang, Jiacheng
Deng, Lei
author_sort Liu, Minghui
collection PubMed
description BACKGROUND: Studies have found that miRNAs play an important role in many biological activities involved in human diseases. Revealing the associations between miRNA and disease by biological experiments is time-consuming and expensive. The computational approaches provide a new alternative. However, because of the limited knowledge of the associations between miRNAs and diseases, it is difficult to support the prediction model effectively. METHODS: In this work, we propose a model to predict miRNA-disease associations, MDAPCOM, in which protein information associated with miRNAs and diseases is introduced to build a global miRNA-protein-disease network. Subsequently, diffusion features and HeteSim features, extracted from the global network, are combined to train the prediction model by eXtreme Gradient Boosting (XGBoost). RESULTS: The MDAPCOM model achieves AUC of 0.991 based on 10-fold cross-validation, which is significantly better than that of other two state-of-the-art methods RWRMDA and PRINCE. Furthermore, the model performs well on three unbalanced data sets. CONCLUSIONS: The results suggest that the information behind proteins associated with miRNAs and diseases is crucial to the prediction of the associations between miRNAs and diseases, and the hybrid feature representation in the heterogeneous network is very effective for improving predictive performance.
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spelling pubmed-75799812020-10-22 Predicting miRNA-disease associations using a hybrid feature representation in the heterogeneous network Liu, Minghui Yang, Jingyi Wang, Jiacheng Deng, Lei BMC Med Genomics Research BACKGROUND: Studies have found that miRNAs play an important role in many biological activities involved in human diseases. Revealing the associations between miRNA and disease by biological experiments is time-consuming and expensive. The computational approaches provide a new alternative. However, because of the limited knowledge of the associations between miRNAs and diseases, it is difficult to support the prediction model effectively. METHODS: In this work, we propose a model to predict miRNA-disease associations, MDAPCOM, in which protein information associated with miRNAs and diseases is introduced to build a global miRNA-protein-disease network. Subsequently, diffusion features and HeteSim features, extracted from the global network, are combined to train the prediction model by eXtreme Gradient Boosting (XGBoost). RESULTS: The MDAPCOM model achieves AUC of 0.991 based on 10-fold cross-validation, which is significantly better than that of other two state-of-the-art methods RWRMDA and PRINCE. Furthermore, the model performs well on three unbalanced data sets. CONCLUSIONS: The results suggest that the information behind proteins associated with miRNAs and diseases is crucial to the prediction of the associations between miRNAs and diseases, and the hybrid feature representation in the heterogeneous network is very effective for improving predictive performance. BioMed Central 2020-10-22 /pmc/articles/PMC7579981/ /pubmed/33087118 http://dx.doi.org/10.1186/s12920-020-00783-0 Text en © The Author(s) 2020 Open Access This 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/. 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 in a credit line to the data.
spellingShingle Research
Liu, Minghui
Yang, Jingyi
Wang, Jiacheng
Deng, Lei
Predicting miRNA-disease associations using a hybrid feature representation in the heterogeneous network
title Predicting miRNA-disease associations using a hybrid feature representation in the heterogeneous network
title_full Predicting miRNA-disease associations using a hybrid feature representation in the heterogeneous network
title_fullStr Predicting miRNA-disease associations using a hybrid feature representation in the heterogeneous network
title_full_unstemmed Predicting miRNA-disease associations using a hybrid feature representation in the heterogeneous network
title_short Predicting miRNA-disease associations using a hybrid feature representation in the heterogeneous network
title_sort predicting mirna-disease associations using a hybrid feature representation in the heterogeneous network
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7579981/
https://www.ncbi.nlm.nih.gov/pubmed/33087118
http://dx.doi.org/10.1186/s12920-020-00783-0
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