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Genomics is the science of genomes: it is the study of all the genetic material of an organism. In humans, the genome consists of information carried in 23 pairs of chromosomes in the nucleus, as well as mitochondrial DNA. In genomics, both coding and non-coding DNA is sequenced and analyzed. Genomics allows a better understanding of all living things, their evolution, and their diversity. It has a myriad of uses: for example, to build phylogenetic trees, to improve productivity and...
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Related Experiment Video

Updated: Aug 16, 2025

In Silico Identification and Characterization of circRNAs During Host-Pathogen Interactions
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In Silico Identification and Characterization of circRNAs During Host-Pathogen Interactions

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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
PubMed
Summary
This summary is machine-generated.

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.

Keywords:
CircRNACircRNA–disease associationDiseaseGraph attention networkHeterogeneous graph neural network

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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.