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FCMDAP: using miRNA family and cluster information to improve the prediction accuracy of disease related miRNAs

BACKGROUND: Biological experiments have confirmed the association between miRNAs and various diseases. However, such experiments are costly and time consuming. Computational methods help select potential disease-related miRNAs to improve the efficiency of biological experiments. METHODS: In this wor...

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Detalles Bibliográficos
Autores principales: Li, Xiaoying, Lin, Yaping, Gu, Changlong, Yang, Jialiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6449885/
https://www.ncbi.nlm.nih.gov/pubmed/30953512
http://dx.doi.org/10.1186/s12918-019-0696-9
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author Li, Xiaoying
Lin, Yaping
Gu, Changlong
Yang, Jialiang
author_facet Li, Xiaoying
Lin, Yaping
Gu, Changlong
Yang, Jialiang
author_sort Li, Xiaoying
collection PubMed
description BACKGROUND: Biological experiments have confirmed the association between miRNAs and various diseases. However, such experiments are costly and time consuming. Computational methods help select potential disease-related miRNAs to improve the efficiency of biological experiments. METHODS: In this work, we develop a novel method using multiple types of data to calculate miRNA and disease similarity based on mutual information, and add miRNA family and cluster information to predict human disease-related miRNAs (FCMDAP). This method not only depends on known miRNA-diseases associations but also accurately measures miRNA and disease similarity and resolves the problem of overestimation. FCMDAP uses the k most similar neighbor recommendation algorithm to predict the association score between miRNA and disease. Information about miRNA cluster is also used to improve prediction accuracy. RESULT: FCMDAP achieves an average AUC of 0.9165 based on leave-one-out cross validation. Results confirm the 100, 98 and 96% of the top 50 predicted miRNAs reported in case studies on colorectal, lung, and pancreatic neoplasms. FCMDAP also exhibits satisfactory performance in predicting diseases without any related miRNAs and miRNAs without any related diseases. CONCLUSIONS: In this study, we present a computational method FCMDAP to improve the prediction accuracy of disease related miRNAs. FCMDAP could be an effective tool for further biological experiments. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12918-019-0696-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-64498852019-04-15 FCMDAP: using miRNA family and cluster information to improve the prediction accuracy of disease related miRNAs Li, Xiaoying Lin, Yaping Gu, Changlong Yang, Jialiang BMC Syst Biol Research BACKGROUND: Biological experiments have confirmed the association between miRNAs and various diseases. However, such experiments are costly and time consuming. Computational methods help select potential disease-related miRNAs to improve the efficiency of biological experiments. METHODS: In this work, we develop a novel method using multiple types of data to calculate miRNA and disease similarity based on mutual information, and add miRNA family and cluster information to predict human disease-related miRNAs (FCMDAP). This method not only depends on known miRNA-diseases associations but also accurately measures miRNA and disease similarity and resolves the problem of overestimation. FCMDAP uses the k most similar neighbor recommendation algorithm to predict the association score between miRNA and disease. Information about miRNA cluster is also used to improve prediction accuracy. RESULT: FCMDAP achieves an average AUC of 0.9165 based on leave-one-out cross validation. Results confirm the 100, 98 and 96% of the top 50 predicted miRNAs reported in case studies on colorectal, lung, and pancreatic neoplasms. FCMDAP also exhibits satisfactory performance in predicting diseases without any related miRNAs and miRNAs without any related diseases. CONCLUSIONS: In this study, we present a computational method FCMDAP to improve the prediction accuracy of disease related miRNAs. FCMDAP could be an effective tool for further biological experiments. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12918-019-0696-9) contains supplementary material, which is available to authorized users. BioMed Central 2019-04-05 /pmc/articles/PMC6449885/ /pubmed/30953512 http://dx.doi.org/10.1186/s12918-019-0696-9 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 Research
Li, Xiaoying
Lin, Yaping
Gu, Changlong
Yang, Jialiang
FCMDAP: using miRNA family and cluster information to improve the prediction accuracy of disease related miRNAs
title FCMDAP: using miRNA family and cluster information to improve the prediction accuracy of disease related miRNAs
title_full FCMDAP: using miRNA family and cluster information to improve the prediction accuracy of disease related miRNAs
title_fullStr FCMDAP: using miRNA family and cluster information to improve the prediction accuracy of disease related miRNAs
title_full_unstemmed FCMDAP: using miRNA family and cluster information to improve the prediction accuracy of disease related miRNAs
title_short FCMDAP: using miRNA family and cluster information to improve the prediction accuracy of disease related miRNAs
title_sort fcmdap: using mirna family and cluster information to improve the prediction accuracy of disease related mirnas
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6449885/
https://www.ncbi.nlm.nih.gov/pubmed/30953512
http://dx.doi.org/10.1186/s12918-019-0696-9
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