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Adaptive multi-view multi-label learning for identifying disease-associated candidate miRNAs
Increasing evidence has indicated that microRNAs(miRNAs) play vital roles in various pathological processes and thus are closely related with many complex human diseases. The identification of potential disease-related miRNAs offers new opportunities to understand disease etiology and pathogenesis....
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6459551/ https://www.ncbi.nlm.nih.gov/pubmed/30933970 http://dx.doi.org/10.1371/journal.pcbi.1006931 |
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author | Liang, Cheng Yu, Shengpeng Luo, Jiawei |
author_facet | Liang, Cheng Yu, Shengpeng Luo, Jiawei |
author_sort | Liang, Cheng |
collection | PubMed |
description | Increasing evidence has indicated that microRNAs(miRNAs) play vital roles in various pathological processes and thus are closely related with many complex human diseases. The identification of potential disease-related miRNAs offers new opportunities to understand disease etiology and pathogenesis. Although there have been numerous computational methods proposed to predict reliable miRNA-disease associations, they suffer from various limitations that affect the prediction accuracy and their applicability. In this study, we develop a novel method to discover disease-related candidate miRNAs based on Adaptive Multi-View Multi-Label learning(AMVML). Specifically, considering the inherent noise existed in the current dataset, we propose to learn a new affinity graph adaptively for both diseases and miRNAs from multiple similarity profiles. We then simultaneously update the miRNA-disease association predicted from both spaces based on multi-label learning. In particular, we prove the convergence of AMVML theoretically and the corresponding analysis indicates that it has a fast convergence rate. To comprehensively illustrate the prediction performance of our method, we compared AMVML with four state-of-the-art methods under different validation frameworks. As a result, our method achieved comparable performance under various evaluation metrics, which suggests that our method is capable of discovering greater number of true miRNA-disease associations. The case study conducted on thyroid neoplasms further identified a potential diagnostic biomarker. Together, the experimental results confirms the utility of our method and we anticipate that our method could serve as a reliable and efficient tool for uncovering novel disease-related miRNAs. |
format | Online Article Text |
id | pubmed-6459551 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-64595512019-05-03 Adaptive multi-view multi-label learning for identifying disease-associated candidate miRNAs Liang, Cheng Yu, Shengpeng Luo, Jiawei PLoS Comput Biol Research Article Increasing evidence has indicated that microRNAs(miRNAs) play vital roles in various pathological processes and thus are closely related with many complex human diseases. The identification of potential disease-related miRNAs offers new opportunities to understand disease etiology and pathogenesis. Although there have been numerous computational methods proposed to predict reliable miRNA-disease associations, they suffer from various limitations that affect the prediction accuracy and their applicability. In this study, we develop a novel method to discover disease-related candidate miRNAs based on Adaptive Multi-View Multi-Label learning(AMVML). Specifically, considering the inherent noise existed in the current dataset, we propose to learn a new affinity graph adaptively for both diseases and miRNAs from multiple similarity profiles. We then simultaneously update the miRNA-disease association predicted from both spaces based on multi-label learning. In particular, we prove the convergence of AMVML theoretically and the corresponding analysis indicates that it has a fast convergence rate. To comprehensively illustrate the prediction performance of our method, we compared AMVML with four state-of-the-art methods under different validation frameworks. As a result, our method achieved comparable performance under various evaluation metrics, which suggests that our method is capable of discovering greater number of true miRNA-disease associations. The case study conducted on thyroid neoplasms further identified a potential diagnostic biomarker. Together, the experimental results confirms the utility of our method and we anticipate that our method could serve as a reliable and efficient tool for uncovering novel disease-related miRNAs. Public Library of Science 2019-04-01 /pmc/articles/PMC6459551/ /pubmed/30933970 http://dx.doi.org/10.1371/journal.pcbi.1006931 Text en © 2019 Liang et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Liang, Cheng Yu, Shengpeng Luo, Jiawei Adaptive multi-view multi-label learning for identifying disease-associated candidate miRNAs |
title | Adaptive multi-view multi-label learning for identifying disease-associated candidate miRNAs |
title_full | Adaptive multi-view multi-label learning for identifying disease-associated candidate miRNAs |
title_fullStr | Adaptive multi-view multi-label learning for identifying disease-associated candidate miRNAs |
title_full_unstemmed | Adaptive multi-view multi-label learning for identifying disease-associated candidate miRNAs |
title_short | Adaptive multi-view multi-label learning for identifying disease-associated candidate miRNAs |
title_sort | adaptive multi-view multi-label learning for identifying disease-associated candidate mirnas |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6459551/ https://www.ncbi.nlm.nih.gov/pubmed/30933970 http://dx.doi.org/10.1371/journal.pcbi.1006931 |
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