LWPCMF: Logistic Weighted Profile-Based Collaborative Matrix Factorization for Predicting MiRNA-Disease Associations

被引:14
作者
Yin, Meng-Meng [1 ]
Cui, Zhen [1 ]
Gao, Ming-Ming [1 ]
Liu, Jin-Xing [1 ]
Gao, Ying-Lian [2 ]
机构
[1] Qufu Normal Univ, Sch Informat Sci & Engn, Rizhao 276826, Shandong, Peoples R China
[2] Qufu Normal Univ, Lib, Rizhao 276826, Shandong, Peoples R China
基金
美国国家科学基金会;
关键词
Diseases; Kernel; Logistics; Semantics; Computational modeling; Databases; Collaboration; miRNA-disease association; collaborative matrix factorization; logistic function; weighted profile; MICRORNA DEREGULATION;
D O I
10.1109/TCBB.2019.2937774
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
As is known to all, constructing experiments to predict unknown miRNA-disease association is time-consuming, laborious and costly. Accordingly, new prediction model should be conducted to predict novel miRNA-disease associations. What's more, the performance of this method should be high and reliable. In this paper, a new computation model Logistic Weighted Profile-based Collaborative Matrix Factorization (LWPCMF) is put forward. In this method, weighted profile (WP) is combined with collaborative matrix factorization (CMF) to increase the performance of this model. And, the neighbor information is considered. In addition, logistic function is applied to miRNA functional similarity matrix and disease semantic similarity matrix to extract valuable information. At the same time, by adding WP and logistic function, the known correlation can be protected. And, Gaussian Interaction Profile (GIP) kernels of miRNAs and diseases are added to miRNA functional similarity network and disease semantic similarity network to augment kernel similarities. Then, a five-fold cross validation is implemented to evaluate the predictive ability of this method. Besides, case studies are conducted to view the experimental results. The final result contains not only known associations but also newly predicted ones. And, the result proves that our method is better than other existing methods. This model is able to predict potential miRNA-disease associations.
引用
收藏
页码:1122 / 1129
页数:8
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