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NPCMF: Nearest Profile-based Collaborative Matrix Factorization method for predicting miRNA-disease associations
BACKGROUND: Predicting meaningful miRNA-disease associations (MDAs) is costly. Therefore, an increasing number of researchers are beginning to focus on methods to predict potential MDAs. Thus, prediction methods with improved accuracy are under development. An efficient computational method is propo...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6591872/ https://www.ncbi.nlm.nih.gov/pubmed/31234797 http://dx.doi.org/10.1186/s12859-019-2956-5 |
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author | Gao, Ying-Lian Cui, Zhen Liu, Jin-Xing Wang, Juan Zheng, Chun-Hou |
author_facet | Gao, Ying-Lian Cui, Zhen Liu, Jin-Xing Wang, Juan Zheng, Chun-Hou |
author_sort | Gao, Ying-Lian |
collection | PubMed |
description | BACKGROUND: Predicting meaningful miRNA-disease associations (MDAs) is costly. Therefore, an increasing number of researchers are beginning to focus on methods to predict potential MDAs. Thus, prediction methods with improved accuracy are under development. An efficient computational method is proposed to be crucial for predicting novel MDAs. For improved experimental productivity, large biological datasets are used by researchers. Although there are many effective and feasible methods to predict potential MDAs, the possibility remains that these methods are flawed. RESULTS: A simple and effective method, known as Nearest Profile-based Collaborative Matrix Factorization (NPCMF), is proposed to identify novel MDAs. The nearest profile is introduced to our method to achieve the highest AUC value compared with other advanced methods. For some miRNAs and diseases without any association, we use the nearest neighbour information to complete the prediction. CONCLUSIONS: To evaluate the performance of our method, five-fold cross-validation is used to calculate the AUC value. At the same time, three disease cases, gastric neoplasms, rectal neoplasms and colonic neoplasms, are used to predict novel MDAs on a gold-standard dataset. We predict the vast majority of known MDAs and some novel MDAs. Finally, the prediction accuracy of our method is determined to be better than that of other existing methods. Thus, the proposed prediction model can obtain reliable experimental results. |
format | Online Article Text |
id | pubmed-6591872 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-65918722019-07-08 NPCMF: Nearest Profile-based Collaborative Matrix Factorization method for predicting miRNA-disease associations Gao, Ying-Lian Cui, Zhen Liu, Jin-Xing Wang, Juan Zheng, Chun-Hou BMC Bioinformatics Methodology Article BACKGROUND: Predicting meaningful miRNA-disease associations (MDAs) is costly. Therefore, an increasing number of researchers are beginning to focus on methods to predict potential MDAs. Thus, prediction methods with improved accuracy are under development. An efficient computational method is proposed to be crucial for predicting novel MDAs. For improved experimental productivity, large biological datasets are used by researchers. Although there are many effective and feasible methods to predict potential MDAs, the possibility remains that these methods are flawed. RESULTS: A simple and effective method, known as Nearest Profile-based Collaborative Matrix Factorization (NPCMF), is proposed to identify novel MDAs. The nearest profile is introduced to our method to achieve the highest AUC value compared with other advanced methods. For some miRNAs and diseases without any association, we use the nearest neighbour information to complete the prediction. CONCLUSIONS: To evaluate the performance of our method, five-fold cross-validation is used to calculate the AUC value. At the same time, three disease cases, gastric neoplasms, rectal neoplasms and colonic neoplasms, are used to predict novel MDAs on a gold-standard dataset. We predict the vast majority of known MDAs and some novel MDAs. Finally, the prediction accuracy of our method is determined to be better than that of other existing methods. Thus, the proposed prediction model can obtain reliable experimental results. BioMed Central 2019-06-24 /pmc/articles/PMC6591872/ /pubmed/31234797 http://dx.doi.org/10.1186/s12859-019-2956-5 Text en © The Author(s). 2019 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 Gao, Ying-Lian Cui, Zhen Liu, Jin-Xing Wang, Juan Zheng, Chun-Hou NPCMF: Nearest Profile-based Collaborative Matrix Factorization method for predicting miRNA-disease associations |
title | NPCMF: Nearest Profile-based Collaborative Matrix Factorization method for predicting miRNA-disease associations |
title_full | NPCMF: Nearest Profile-based Collaborative Matrix Factorization method for predicting miRNA-disease associations |
title_fullStr | NPCMF: Nearest Profile-based Collaborative Matrix Factorization method for predicting miRNA-disease associations |
title_full_unstemmed | NPCMF: Nearest Profile-based Collaborative Matrix Factorization method for predicting miRNA-disease associations |
title_short | NPCMF: Nearest Profile-based Collaborative Matrix Factorization method for predicting miRNA-disease associations |
title_sort | npcmf: nearest profile-based collaborative matrix factorization method for predicting mirna-disease associations |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6591872/ https://www.ncbi.nlm.nih.gov/pubmed/31234797 http://dx.doi.org/10.1186/s12859-019-2956-5 |
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