miRNA-Disease Association Prediction with Collaborative Matrix Factorization
As one of the factors in the noncoding RNA family, microRNAs (miRNAs) are involved in the development and progression of various complex diseases. Experimental identification of miRNA-disease association is expensive and time-consuming. Therefore, it is necessary to design efficient algorithms to id...
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doaj-3dcfe21a3f5e4717ae08d08c3cb979a12020-11-25T01:58:57ZengHindawi-WileyComplexity1076-27871099-05262017-01-01201710.1155/2017/24989572498957miRNA-Disease Association Prediction with Collaborative Matrix FactorizationZhen Shen0You-Hua Zhang1Kyungsook Han2Asoke K. Nandi3Barry Honig4De-Shuang Huang5Institute of Machine Learning and Systems Biology, School of Electronics and Information Engineering, Tongji University, Shanghai 201804, ChinaSchool of Information and Computer, Anhui Agricultural University, Changjiang West Road 130, Hefei, Anhui, ChinaDepartment of Computer Science and Engineering, Inha University, Incheon, Republic of KoreaDepartment of Electronic and Computer Engineering, Brunel University London, Uxbridge UB8 3PH, UKCenter for Computational Biology and Bioinformatics, Columbia University, 1130 St. Nicholas Avenue, Room 815, New York, NY 10032, USAInstitute of Machine Learning and Systems Biology, School of Electronics and Information Engineering, Tongji University, Shanghai 201804, ChinaAs one of the factors in the noncoding RNA family, microRNAs (miRNAs) are involved in the development and progression of various complex diseases. Experimental identification of miRNA-disease association is expensive and time-consuming. Therefore, it is necessary to design efficient algorithms to identify novel miRNA-disease association. In this paper, we developed the computational method of Collaborative Matrix Factorization for miRNA-Disease Association prediction (CMFMDA) to identify potential miRNA-disease associations by integrating miRNA functional similarity, disease semantic similarity, and experimentally verified miRNA-disease associations. Experiments verified that CMFMDA achieves intended purpose and application values with its short consuming-time and high prediction accuracy. In addition, we used CMFMDA on Esophageal Neoplasms and Kidney Neoplasms to reveal their potential related miRNAs. As a result, 84% and 82% of top 50 predicted miRNA-disease pairs for these two diseases were confirmed by experiment. Not only this, but also CMFMDA could be applied to new diseases and new miRNAs without any known associations, which overcome the defects of many previous computational methods.http://dx.doi.org/10.1155/2017/2498957 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Zhen Shen You-Hua Zhang Kyungsook Han Asoke K. Nandi Barry Honig De-Shuang Huang |
spellingShingle |
Zhen Shen You-Hua Zhang Kyungsook Han Asoke K. Nandi Barry Honig De-Shuang Huang miRNA-Disease Association Prediction with Collaborative Matrix Factorization Complexity |
author_facet |
Zhen Shen You-Hua Zhang Kyungsook Han Asoke K. Nandi Barry Honig De-Shuang Huang |
author_sort |
Zhen Shen |
title |
miRNA-Disease Association Prediction with Collaborative Matrix Factorization |
title_short |
miRNA-Disease Association Prediction with Collaborative Matrix Factorization |
title_full |
miRNA-Disease Association Prediction with Collaborative Matrix Factorization |
title_fullStr |
miRNA-Disease Association Prediction with Collaborative Matrix Factorization |
title_full_unstemmed |
miRNA-Disease Association Prediction with Collaborative Matrix Factorization |
title_sort |
mirna-disease association prediction with collaborative matrix factorization |
publisher |
Hindawi-Wiley |
series |
Complexity |
issn |
1076-2787 1099-0526 |
publishDate |
2017-01-01 |
description |
As one of the factors in the noncoding RNA family, microRNAs (miRNAs) are involved in the development and progression of various complex diseases. Experimental identification of miRNA-disease association is expensive and time-consuming. Therefore, it is necessary to design efficient algorithms to identify novel miRNA-disease association. In this paper, we developed the computational method of Collaborative Matrix Factorization for miRNA-Disease Association prediction (CMFMDA) to identify potential miRNA-disease associations by integrating miRNA functional similarity, disease semantic similarity, and experimentally verified miRNA-disease associations. Experiments verified that CMFMDA achieves intended purpose and application values with its short consuming-time and high prediction accuracy. In addition, we used CMFMDA on Esophageal Neoplasms and Kidney Neoplasms to reveal their potential related miRNAs. As a result, 84% and 82% of top 50 predicted miRNA-disease pairs for these two diseases were confirmed by experiment. Not only this, but also CMFMDA could be applied to new diseases and new miRNAs without any known associations, which overcome the defects of many previous computational methods. |
url |
http://dx.doi.org/10.1155/2017/2498957 |
work_keys_str_mv |
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1724966952523268096 |