Hessian Regularized L2,1-Nonnegative Matrix Factorization and Deep Learning for miRNA-Disease Associations Prediction

被引:0
|
作者
Han, Guo-Sheng [1 ,2 ,3 ]
Gao, Qi [1 ,2 ,3 ]
Peng, Ling-Zhi [1 ,2 ,3 ]
Tang, Jing [1 ,2 ,3 ]
机构
[1] Xiangtan Univ, Dept Math & Computat Sci, Xiangtan 411105, Peoples R China
[2] Xiangtan Univ, Minist Educ, Key Lab Intelligent Comp & Informat Proc, Xiangtan 411105, Peoples R China
[3] Xiangtan Univ, Hunan Key Lab Computat & Simulat Sci & Engn, Xiangtan 411105, Peoples R China
关键词
miRNA-disease associations; Similarity calculation; Matrix factorization; Deep learning; Singular value decomposition; ARTERY SEGMENTATION; ANGIOGRAPHY; NETWORK; LUMEN; NET;
D O I
10.1007/s12539-023-00594-8
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Since the identification of microRNAs (miRNAs), empirical research has demonstrated their crucial involvement in the functioning of organisms. Investigating miRNAs significantly bolsters efforts related to averting, diagnosing, and treating intricate human maladies. Yet, exploring every conceivable miRNA-disease association consumes significant resources and time within conventional wet experiments. On the computational front, forecasting potential miRNA-disease connections serves as a valuable source of preliminary insights for medical investigators. As a result, we have developed a novel matrix factorization model known as Hessian-regularized L-2,L-1 nonnegative matrix factorization in combination with deep learning for predicting associations between miRNAs and diseases, denoted as HRL2,1-NMF-DF. In particular, we introduce a novel iterative fusion approach to integrate all similarities. This method effectively diminishes the sparsity of the initial miRNA-disease associations matrix. Additionally, we devise a mixed model framework that utilizes deep learning, matrix decompo-sition, and singular value decomposition to capture and depict the intricate nonlinear features of miRNA and disease. The prediction performance of the six matrix factorization methods is improved by comparison and analysis, similarity matrix fusion, data preprocessing, and parameter adjustment. The AUC and AUPR obtained by the new matrix factorization model under fivefold cross validation are comparative or better with other matrix factorization models. Finally, we select three diseases including lung tumor, bladder tumor and breast tumor for case analysis, and further extend the matrix factorization model based on deep learning. The results show that the hybrid algorithm combining matrix factorization with deep learning proposed in this paper can predict miRNAs related to different diseases with high accuracy.{Graphical abstract}
引用
收藏
页码:176 / 191
页数:16
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