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Related Concept Videos

lncRNA - Long Non-coding RNAs02:39

lncRNA - Long Non-coding RNAs

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In humans, more than 80% of the genome gets transcribed. However, only around 2% of the genome codes for proteins. The remaining part produces non-coding RNAs which includes ribosomal RNAs, transfer RNAs, telomerase RNAs, and regulatory RNAs, among other types. A large number of regulatory non-coding RNAs have been classified into two groups depending upon their length – small non-coding RNAs, such as microRNA, which are less than 200 nucleotides in length, and long non-coding RNA...
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Updated: Aug 8, 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

Published on: October 21, 2022

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Collaborative deep learning improves disease-related circRNA prediction based on multi-source functional information.

Yongtian Wang1, Xinmeng Liu1, Yewei Shen1

  • 1School of Computer Science at Northwestern Polytechnical University, Xi'an, China.

Briefings in Bioinformatics
|February 27, 2023
PubMed
Summary
This summary is machine-generated.

This study introduces CLCDA, a novel computational model that leverages multi-view functional annotations of circular RNAs (circRNAs) to predict their associations with diseases. The method enhances disease diagnosis and treatment by identifying previously unknown circRNA-disease links.

Keywords:
circRNAcollaborative deep learningdiseasemulti-view functional annotation

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Area of Science:

  • Genomics
  • Bioinformatics
  • Computational Biology

Background:

  • Circular RNAs (circRNAs) are increasingly recognized for their roles in biological processes and disease.
  • Existing methods for predicting circRNA-disease associations often fail to fully exploit multi-view functional data.
  • Efficiently integrating diverse circRNA data remains a challenge in the field.

Purpose of the Study:

  • To develop a computational model for predicting potential circRNA-disease associations.
  • To effectively utilize multi-view functional annotations of circRNAs for improved prediction accuracy.
  • To enhance the understanding of circRNA roles in disease diagnosis and treatment.

Main Methods:

  • Extraction of circRNA multi-view functional annotations and construction of circRNA association networks.
  • Development of a collaborative deep learning framework for multi-view information integration.
  • Application of a graph autoencoder model for predicting circRNA-disease associations.

Main Results:

  • The proposed CLCDA model demonstrates superior performance in predicting candidate disease-related circRNAs compared to existing methods.
  • Case studies on common diseases identified unknown circRNAs associated with them, showcasing the method's practicability.
  • The model effectively integrates circRNA multi-source information and internal relationships.

Conclusions:

  • CLCDA offers an efficient approach for predicting disease-related circRNAs by leveraging multi-view functional data.
  • The findings support the utility of CLCDA in aiding the diagnosis and treatment of human diseases.
  • This work highlights the potential of collaborative learning frameworks in circRNA research.