Generative Adversarial Matrix Completion Network based on Multi-Source Data Fusion for miRNA-Disease Associations Prediction.


Journal

Briefings in bioinformatics
ISSN: 1477-4054
Titre abrégé: Brief Bioinform
Pays: England
ID NLM: 100912837

Informations de publication

Date de publication:
20 09 2023
Historique:
received: 19 03 2023
revised: 16 06 2023
accepted: 04 07 2023
medline: 25 9 2023
pubmed: 24 7 2023
entrez: 23 7 2023
Statut: ppublish

Résumé

Numerous biological studies have shown that considering disease-associated micro RNAs (miRNAs) as potential biomarkers or therapeutic targets offers new avenues for the diagnosis of complex diseases. Computational methods have gradually been introduced to reveal disease-related miRNAs. Considering that previous models have not fused sufficiently diverse similarities, that their inappropriate fusion methods may lead to poor quality of the comprehensive similarity network and that their results are often limited by insufficiently known associations, we propose a computational model called Generative Adversarial Matrix Completion Network based on Multi-source Data Fusion (GAMCNMDF) for miRNA-disease association prediction. We create a diverse network connecting miRNAs and diseases, which is then represented using a matrix. The main task of GAMCNMDF is to complete the matrix and obtain the predicted results. The main innovations of GAMCNMDF are reflected in two aspects: GAMCNMDF integrates diverse data sources and employs a nonlinear fusion approach to update the similarity networks of miRNAs and diseases. Also, some additional information is provided to GAMCNMDF in the form of a 'hint' so that GAMCNMDF can work successfully even when complete data are not available. Compared with other methods, the outcomes of 10-fold cross-validation on two distinct databases validate the superior performance of GAMCNMDF with statistically significant results. It is worth mentioning that we apply GAMCNMDF in the identification of underlying small molecule-related miRNAs, yielding outstanding performance results in this specific domain. In addition, two case studies about two important neoplasms show that GAMCNMDF is a promising prediction method.

Identifiants

pubmed: 37482409
pii: 7229684
doi: 10.1093/bib/bbad270
pii:
doi:

Substances chimiques

MicroRNAs 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2023. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

Auteurs

ShuDong Wang (S)

College of Computer Science and Technology, Qingdao Institute of Software, China University of Petroleum (East China), 66 Changjiang Xi Lu, 266580, Shandong, China.

YunYin Li (Y)

College of Computer Science and Technology, Qingdao Institute of Software, China University of Petroleum (East China), 66 Changjiang Xi Lu, 266580, Shandong, China.

YuanYuan Zhang (Y)

College of Computer Science and Technology, Qingdao Institute of Software, China University of Petroleum (East China), 66 Changjiang Xi Lu, 266580, Shandong, China.

ShanChen Pang (S)

College of Computer Science and Technology, Qingdao Institute of Software, China University of Petroleum (East China), 66 Changjiang Xi Lu, 266580, Shandong, China.

SiBo Qiao (S)

College of Computer Science and Technology, Qingdao Institute of Software, China University of Petroleum (East China), 66 Changjiang Xi Lu, 266580, Shandong, China.

Yu Zhang (Y)

College of Computer Science and Technology, Qingdao Institute of Software, China University of Petroleum (East China), 66 Changjiang Xi Lu, 266580, Shandong, China.

FuYu Wang (F)

College of Computer Science and Technology, Qingdao Institute of Software, China University of Petroleum (East China), 66 Changjiang Xi Lu, 266580, Shandong, China.

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