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DRGCNCDA: Predicting circRNA-disease interactions based on knowledge graph and disentangled relational graph
Wei Lan1, Hongyu Zhang2, Yi Dong2
1School of Computer, Electronic and Information, Guangxi University, Nanning, China; Guangxi Key Laboratory of Multimedia Communications and Network Technology, Guangxi University, Nanning, China.
Insights
A new computational model, DRGCNCDA, enhances prediction of circular RNA (circRNA) and disease associations by integrating multiple biological relationships. This method outperforms existing models, offering reliable candidates for future biological experiments.
Area of Science:
- Genomics
- Bioinformatics
- Computational Biology
Background:
- Circular RNAs (circRNAs) are increasingly recognized for their roles in human disease diagnosis and prognosis.
- Existing computational methods for predicting circRNA-disease associations often overlook interactions with other biological entities and latent factors.
Purpose of the Study:
- To propose a novel computational model, DRGCNCDA, to address limitations in current circRNA-disease association prediction.
- To improve the accuracy and comprehensiveness of predicting circRNA-disease associations by incorporating multi-relational data.
Main Methods:
- Constructed multi-relational graphs integrating circRNA, disease, miRNA, and lncRNA data.
- Employed a disentangled relational graph convolutional network (DRGCNCDA) to derive feature vectors for circRNAs and diseases.
- Utilized a knowledge graph model to predict circRNA-disease association affinity scores based on learned embeddings.
Main Results:
- The DRGCNCDA model demonstrated superior performance compared to existing computational methods.
- Experimental validation using 5-fold cross-validation confirmed the model's effectiveness.
- A case study highlighted the model's capability in predicting circRNA-disease associations and identifying potential candidates for biological experiments.
Conclusions:
- The DRGCNCDA model offers a significant advancement in predicting circRNA-disease associations.
- The integration of multi-relational data and advanced network techniques enhances prediction accuracy.
- DRGCNCDA provides a valuable tool for biological research, aiding in the identification of potential disease-related circRNAs.
Abstract:
Emerging studies have shown that circular RNA (circRNA) plays a significant role in the diagnosis and prognosis of human disease. Some computational methods have been proposed to predict circRNA-disease associations. However, some methods only use circRNA-disease association and ignore the associations of other biological entities. In addition, these methods do not take into account the latent factors of different kinds of circRNAs and diseases. To solve these limitations of existing computational models, we propose a new computational model (DRGCNCDA) based on disentangled relational graph convolutional network. The circRNA-disease multi-relational graphs are constructed by collecting multiple relational data among circRNA, disease, miRNA and lncRNA. Then, the disentangled relational graph convolutional network is employed to obtain the feature vectors of circRNA and disease. Finally, knowledge graph model is applied to predict the affinity scores of circRNA-disease associations based on the embeddings of circRNA and disease. The 5-fold cross validation is utilized to evaluate the performance of the method. The experimental results show that the DRGCNCDA outperforms other existing models. Moreover, the case study demonstrates that the DRGCNCDA is effective to predict the circRNA-disease association and can provide reliable candidates for biological experiments.
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