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Updated: Aug 16, 2025

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In Silico Identification and Characterization of circRNAs During Host-Pathogen Interactions
Published on: October 21, 2022
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Inferring disease-associated circRNAs by multi-source aggregation based on heterogeneous graph neural network.
Chengqian Lu1,2,3, Lishen Zhang1,2, Min Zeng1,2
1School of Computer Science and Engineering, Central South University, Changsha, 410083, Hunan, China.
Briefings in Bioinformatics
|December 26, 2022
Summary
Circular RNAs (circRNAs) are key in disease. Our new computational model, CDHGNN, accurately predicts circRNA-disease links using heterogeneous graph neural networks, offering a cost-effective diagnostic tool.
Area of Science:
- Bioinformatics
- Computational Biology
- Genomics
Background:
- Circular RNAs (circRNAs) are increasingly recognized for their roles in disease pathogenesis.
- Their unique structure makes them promising biomarkers for diagnosis.
- Computational methods offer a cost-effective alternative to traditional experiments for identifying circRNA-disease associations.
Purpose of the Study:
- To develop an effective computational model for predicting circRNA-disease associations.
- To address the limitations of existing methods that overlook data heterogeneity.
- To leverage multi-source pathogenesis data for robust association inference.
Main Methods:
- Proposed a novel model, CDHGNN, utilizing edge-weighted graph attention and heterogeneous graph neural networks.
- Constructed integrated networks including circRNA, microRNA, disease, and heterogeneous networks from multi-source data.
- Employed an edge-weighted graph attention network for node feature representation and heterogeneous neural networks for association prediction.
Main Results:
- CDHGNN demonstrated superior accuracy in predicting circRNA-disease associations compared to state-of-the-art algorithms.
- Both edge-weighted graph attention and heterogeneous graph networks significantly improved model performance.
- Case studies validated CDHGNN's ability to identify specific molecular associations and regulatory relationships.
Conclusions:
- CDHGNN provides an effective and accurate computational approach for circRNA-disease association prediction.
- The model's ability to integrate heterogeneous data enhances the inference of complex biomolecular relationships.
- This work contributes a valuable tool for advancing our understanding of circRNA functions in pathogenesis.
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