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PMAMCA: prediction of microRNA-disease association utilizing a matrix completion approach

BACKGROUND: Numerous experimental results have indicated that microRNAs (miRNAs) play a vital role in biological processes, as well as outbreaks of diseases at the molecular level. Despite their important role in biological processes, knowledge regarding specific functions of miRNAs in the developme...

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Autores principales: Ha, Jihwan, Park, Chihyun, Park, Sanghyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6425656/
https://www.ncbi.nlm.nih.gov/pubmed/30894171
http://dx.doi.org/10.1186/s12918-019-0700-4
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author Ha, Jihwan
Park, Chihyun
Park, Sanghyun
author_facet Ha, Jihwan
Park, Chihyun
Park, Sanghyun
author_sort Ha, Jihwan
collection PubMed
description BACKGROUND: Numerous experimental results have indicated that microRNAs (miRNAs) play a vital role in biological processes, as well as outbreaks of diseases at the molecular level. Despite their important role in biological processes, knowledge regarding specific functions of miRNAs in the development of human diseases is very limited. While attempting to solve this problem, many computational approaches have been proposed and attracted significant attention. However, most previous approaches suffer from the common problem of being inapplicable to new diseases without any known miRNA-disease associations. RESULTS: This paper proposes a novel method for inferring disease-miRNA associations utilizing a machine learning technique called matrix factorization, which is widely used in recommendation systems. In recommendation systems, the goal is to predict rating scores that a user might assign to specific items. By replacing users with miRNAs and items with diseases, we can efficiently predict miRNA-disease associations without seed miRNAs. As a result, our proposed model, called prediction of microRNA-disease association utilizing a matrix completion approach, achieves excellent performance compared to previous approaches with a reliable AUC value of 0.882 by implementing five-fold cross validation. CONCLUSIONS: To the best of our knowledge, the proposed method applies the matrix completion technique to infer miRNA-disease associations and overcome the seed-miRNA problem negatively affects existing computational models. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12918-019-0700-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-64256562019-04-01 PMAMCA: prediction of microRNA-disease association utilizing a matrix completion approach Ha, Jihwan Park, Chihyun Park, Sanghyun BMC Syst Biol Research Article BACKGROUND: Numerous experimental results have indicated that microRNAs (miRNAs) play a vital role in biological processes, as well as outbreaks of diseases at the molecular level. Despite their important role in biological processes, knowledge regarding specific functions of miRNAs in the development of human diseases is very limited. While attempting to solve this problem, many computational approaches have been proposed and attracted significant attention. However, most previous approaches suffer from the common problem of being inapplicable to new diseases without any known miRNA-disease associations. RESULTS: This paper proposes a novel method for inferring disease-miRNA associations utilizing a machine learning technique called matrix factorization, which is widely used in recommendation systems. In recommendation systems, the goal is to predict rating scores that a user might assign to specific items. By replacing users with miRNAs and items with diseases, we can efficiently predict miRNA-disease associations without seed miRNAs. As a result, our proposed model, called prediction of microRNA-disease association utilizing a matrix completion approach, achieves excellent performance compared to previous approaches with a reliable AUC value of 0.882 by implementing five-fold cross validation. CONCLUSIONS: To the best of our knowledge, the proposed method applies the matrix completion technique to infer miRNA-disease associations and overcome the seed-miRNA problem negatively affects existing computational models. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12918-019-0700-4) contains supplementary material, which is available to authorized users. BioMed Central 2019-03-20 /pmc/articles/PMC6425656/ /pubmed/30894171 http://dx.doi.org/10.1186/s12918-019-0700-4 Text en © The Author(s). 2019 Open Access This 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 Research Article
Ha, Jihwan
Park, Chihyun
Park, Sanghyun
PMAMCA: prediction of microRNA-disease association utilizing a matrix completion approach
title PMAMCA: prediction of microRNA-disease association utilizing a matrix completion approach
title_full PMAMCA: prediction of microRNA-disease association utilizing a matrix completion approach
title_fullStr PMAMCA: prediction of microRNA-disease association utilizing a matrix completion approach
title_full_unstemmed PMAMCA: prediction of microRNA-disease association utilizing a matrix completion approach
title_short PMAMCA: prediction of microRNA-disease association utilizing a matrix completion approach
title_sort pmamca: prediction of microrna-disease association utilizing a matrix completion approach
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6425656/
https://www.ncbi.nlm.nih.gov/pubmed/30894171
http://dx.doi.org/10.1186/s12918-019-0700-4
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