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Bipartite graph-based collaborative matrix factorization method for predicting miRNA-disease associations

BACKGROUND: With the rapid development of various advanced biotechnologies, researchers in related fields have realized that microRNAs (miRNAs) play critical roles in many serious human diseases. However, experimental identification of new miRNA–disease associations (MDAs) is expensive and time-cons...

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Autores principales: Zhou, Feng, Yin, Meng-Meng, Jiao, Cui-Na, Cui, Zhen, Zhao, Jing-Xiu, Liu, Jin-Xing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8627000/
https://www.ncbi.nlm.nih.gov/pubmed/34837953
http://dx.doi.org/10.1186/s12859-021-04486-w
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author Zhou, Feng
Yin, Meng-Meng
Jiao, Cui-Na
Cui, Zhen
Zhao, Jing-Xiu
Liu, Jin-Xing
author_facet Zhou, Feng
Yin, Meng-Meng
Jiao, Cui-Na
Cui, Zhen
Zhao, Jing-Xiu
Liu, Jin-Xing
author_sort Zhou, Feng
collection PubMed
description BACKGROUND: With the rapid development of various advanced biotechnologies, researchers in related fields have realized that microRNAs (miRNAs) play critical roles in many serious human diseases. However, experimental identification of new miRNA–disease associations (MDAs) is expensive and time-consuming. Practitioners have shown growing interest in methods for predicting potential MDAs. In recent years, an increasing number of computational methods for predicting novel MDAs have been developed, making a huge contribution to the research of human diseases and saving considerable time. In this paper, we proposed an efficient computational method, named bipartite graph-based collaborative matrix factorization (BGCMF), which is highly advantageous for predicting novel MDAs. RESULTS: By combining two improved recommendation methods, a new model for predicting MDAs is generated. Based on the idea that some new miRNAs and diseases do not have any associations, we adopt the bipartite graph based on the collaborative matrix factorization method to complete the prediction. The BGCMF achieves a desirable result, with AUC of up to 0.9514 ± (0.0007) in the five-fold cross-validation experiments. CONCLUSIONS: Five-fold cross-validation is used to evaluate the capabilities of our method. Simulation experiments are implemented to predict new MDAs. More importantly, the AUC value of our method is higher than those of some state-of-the-art methods. Finally, many associations between new miRNAs and new diseases are successfully predicted by performing simulation experiments, indicating that BGCMF is a useful method to predict more potential miRNAs with roles in various diseases.
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spelling pubmed-86270002021-11-30 Bipartite graph-based collaborative matrix factorization method for predicting miRNA-disease associations Zhou, Feng Yin, Meng-Meng Jiao, Cui-Na Cui, Zhen Zhao, Jing-Xiu Liu, Jin-Xing BMC Bioinformatics Methodology Article BACKGROUND: With the rapid development of various advanced biotechnologies, researchers in related fields have realized that microRNAs (miRNAs) play critical roles in many serious human diseases. However, experimental identification of new miRNA–disease associations (MDAs) is expensive and time-consuming. Practitioners have shown growing interest in methods for predicting potential MDAs. In recent years, an increasing number of computational methods for predicting novel MDAs have been developed, making a huge contribution to the research of human diseases and saving considerable time. In this paper, we proposed an efficient computational method, named bipartite graph-based collaborative matrix factorization (BGCMF), which is highly advantageous for predicting novel MDAs. RESULTS: By combining two improved recommendation methods, a new model for predicting MDAs is generated. Based on the idea that some new miRNAs and diseases do not have any associations, we adopt the bipartite graph based on the collaborative matrix factorization method to complete the prediction. The BGCMF achieves a desirable result, with AUC of up to 0.9514 ± (0.0007) in the five-fold cross-validation experiments. CONCLUSIONS: Five-fold cross-validation is used to evaluate the capabilities of our method. Simulation experiments are implemented to predict new MDAs. More importantly, the AUC value of our method is higher than those of some state-of-the-art methods. Finally, many associations between new miRNAs and new diseases are successfully predicted by performing simulation experiments, indicating that BGCMF is a useful method to predict more potential miRNAs with roles in various diseases. BioMed Central 2021-11-27 /pmc/articles/PMC8627000/ /pubmed/34837953 http://dx.doi.org/10.1186/s12859-021-04486-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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 Methodology Article
Zhou, Feng
Yin, Meng-Meng
Jiao, Cui-Na
Cui, Zhen
Zhao, Jing-Xiu
Liu, Jin-Xing
Bipartite graph-based collaborative matrix factorization method for predicting miRNA-disease associations
title Bipartite graph-based collaborative matrix factorization method for predicting miRNA-disease associations
title_full Bipartite graph-based collaborative matrix factorization method for predicting miRNA-disease associations
title_fullStr Bipartite graph-based collaborative matrix factorization method for predicting miRNA-disease associations
title_full_unstemmed Bipartite graph-based collaborative matrix factorization method for predicting miRNA-disease associations
title_short Bipartite graph-based collaborative matrix factorization method for predicting miRNA-disease associations
title_sort bipartite graph-based collaborative matrix factorization method for predicting mirna-disease associations
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8627000/
https://www.ncbi.nlm.nih.gov/pubmed/34837953
http://dx.doi.org/10.1186/s12859-021-04486-w
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