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KGETCDA: an efficient representation learning framework based on knowledge graph encoder from transformer for

Jinyang Wu1, Zhiwei Ning1, Yidong Ding1

  • 1School of Automation Science and Engineering, Xi'an Jiaotong University, 710049, Shaanxi, China.

Briefings in Bioinformatics
|August 17, 2023
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Summary
This summary is machine-generated.

This study introduces KGETCDA, a novel computational method for identifying circular RNA-disease associations (CDA). KGETCDA leverages a biological knowledge graph and Transformer-based learning to accurately predict disease links, outperforming existing models.

Keywords:
CircRNA-disease associationsHeterogeneous non-coding RNA databaseKnowledge graphTransformerWeb-based visualization

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Area of Science:

  • Bioinformatics
  • Computational Biology
  • Genomics

Background:

  • Circular RNAs (circRNAs) are increasingly recognized for their roles in human disease progression.
  • Efficient identification of circRNA-disease associations (CDAs) is crucial for disease diagnosis and understanding.
  • Existing computational methods for CDA prediction face challenges with data sparsity and capturing complex, high-order interactions.

Purpose of the Study:

  • To develop a novel computational method, KGETCDA, for accurate and efficient prediction of circRNA-disease associations.
  • To address limitations of existing methods, particularly in handling data sparsity and exploring high-order biological information.
  • To provide a user-friendly platform (HNRBase) for accessing and utilizing the developed prediction tool and associated data.

Main Methods:

  • Constructed a large heterogeneous non-coding RNA dataset by integrating over 10 databases.
  • Built a biological knowledge graph incorporating relationships between circRNA, miRNA, lncRNA, and disease.
  • Employed Transformer-based knowledge representation learning and attentive propagation for high-quality embedding generation.
  • Utilized multilayer perceptron for predicting CDA matching scores based on learned embeddings.

Main Results:

  • KGETCDA demonstrated significantly superior performance compared to state-of-the-art models in predicting circRNA-disease associations.
  • The method effectively captured high-order interaction information, overcoming data sparsity limitations.
  • An interactive web platform, HNRBase, was developed for data visualization, download, and prediction, enhancing usability.

Conclusions:

  • KGETCDA offers a powerful and accurate computational approach for identifying circRNA-disease associations.
  • The integration of biological knowledge graphs and advanced learning techniques enhances prediction capabilities.
  • HNRBase provides a valuable resource for researchers studying circRNA functions in human diseases.