Inferring disease-associated circRNAs by multi-source aggregation based on heterogeneous graph neural network

Author:

Lu Chengqian123,Zhang Lishen12,Zeng Min12,Lan Wei4,Duan Guihua12,Wang Jianxin12

Affiliation:

1. Central South University School of Computer Science and Engineering, , Changsha, 410083, Hunan , China

2. Central South University Hunan Provincial Key Lab on Bioinformatics, , Changsha, 410083, Hunan , China

3. Xiangtan University School of Computer Science, , Xiangtan, 411105, Hunan , China

4. Guangxi University School of Computer, Electronic and Information, , Nanning, 530004, Guangxi , China

Abstract

Abstract Emerging evidence has proved that circular RNAs (circRNAs) are implicated in pathogenic processes. They are regarded as promising biomarkers for diagnosis due to covalently closed loop structures. As opposed to traditional experiments, computational approaches can identify circRNA–disease associations at a lower cost. Aggregating multi-source pathogenesis data helps to alleviate data sparsity and infer potential associations at the system level. The majority of computational approaches construct a homologous network using multi-source data, but they lose the heterogeneity of the data. Effective methods that use the features of multi-source data are considered as a matter of urgency. In this paper, we propose a model (CDHGNN) based on edge-weighted graph attention and heterogeneous graph neural networks for potential circRNA–disease association prediction. The circRNA network, micro RNA network, disease network and heterogeneous network are constructed based on multi-source data. To reflect association probabilities between nodes, an edge-weighted graph attention network model is designed for node features. To assign attention weights to different types of edges and learn contextual meta-path, CDHGNN infers potential circRNA–disease association based on heterogeneous neural networks. CDHGNN outperforms state-of-the-art algorithms in terms of accuracy. Edge-weighted graph attention networks and heterogeneous graph networks have both improved performance significantly. Furthermore, case studies suggest that CDHGNN is capable of identifying specific molecular associations and investigating biomolecular regulatory relationships in pathogenesis. The code of CDHGNN is freely available at https://github.com/BioinformaticsCSU/CDHGNN.

Publisher

Oxford University Press (OUP)

Subject

Molecular Biology,Information Systems

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