MSGCL: inferring miRNA–disease associations based on multi-view self-supervised graph structure contrastive learning

Author:

Ruan Xinru1ORCID,Jiang Changzhi1,Lin Peixuan1,Lin Yuan2,Liu Juan34,Huang Shaohui15,Liu Xiangrong15ORCID

Affiliation:

1. Department of Computer Science and Technology, Xiamen University , Xiamen 361005 , China

2. Department of School of Aeronautics and Astronautics, Xiamen University , Xiamen 361005 , China

3. School of economics , innovation, and technology, , Norway

4. Kristiania University college , innovation, and technology, , Norway

5. National Institute for Data Science in Health and Medicine, Xiamen University , Xiamen 361005 , China

Abstract

AbstractPotential miRNA–disease associations (MDA) play an important role in the discovery of complex human disease etiology. Therefore, MDA prediction is an attractive research topic in the field of biomedical machine learning. Recently, several models have been proposed for this task, but their performance limited by over-reliance on relevant network information with noisy graph structure connections. However, the application of self-supervised graph structure learning to MDA tasks remains unexplored. Our study is the first to use multi-view self-supervised contrastive learning (MSGCL) for MDA prediction. Specifically, we generated a learner view without association labels of miRNAs and diseases as input, and utilized the known association network to generate an anchor view that provides guiding signals for the learner view. The graph structure was optimized by designing a contrastive loss to maximize the consistency between the anchor and learner views. Our model is similar to a pre-trained model that continuously optimizes upstream tasks for high-quality association graph topology, thereby enhancing the latent representation of association predictions. The experimental results show that our proposed method outperforms state-of-the-art methods by 2.79$\%$ and 3.20$\%$ in area under the receiver operating characteristic curve (AUC) and area under the precision/recall curve (AUPR), respectively.

Funder

National Natural Science Foundation of China

Zhejiang Lab

Publisher

Oxford University Press (OUP)

Subject

Molecular Biology,Information Systems

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