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Related Concept Videos

MicroRNAs01:22

MicroRNAs

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MicroRNA (miRNA) are short, regulatory RNA transcribed from introns (non-coding regions of a gene) or intergenic regions (stretches of DNA present between genes). Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself, forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After the pre-miRNA...
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MGCNSS: miRNA-disease association prediction with multi-layer graph convolution and distance-based negative sample

Zhen Tian1,2, Chenguang Han1, Lewen Xu1

  • 1School of Computer and Artificial Intelligence, Zhengzhou University, Zhengzhou 450000, China.

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|April 15, 2024
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Summary

This study introduces MGCNSS, a novel method for identifying disease-associated microRNAs (miRNAs) by integrating network analysis and advanced negative sample selection. MGCNSS enhances prediction accuracy for potential miRNA-disease associations, aiding new drug development.

Keywords:
distance-based negative sample selectiongraph convolutional networkmeta-pathmiRNA–disease association

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Area of Science:

  • Biomedical informatics
  • Computational biology
  • Genomics

Background:

  • MicroRNAs (miRNAs) play crucial roles in disease mechanisms, making their identification vital for developing new therapeutics.
  • Network-based methods are common for inferring miRNA-disease associations, but often overlook meta-path importance and reliable negative sample selection.

Purpose of the Study:

  • To propose MGCNSS, a novel approach utilizing multi-layer graph convolution and a high-quality negative sample selection strategy.
  • To improve the accuracy of predicting potential associations between microRNAs and diseases.

Main Methods:

  • Constructing a comprehensive heterogeneous network integrating miRNA and disease similarity with known associations.
  • Employing multi-layer graph convolution to capture diverse meta-path relations and learn miRNA/disease representations.
  • Implementing a negative distance-based sample selection strategy to create a reliable negative sample set.

Main Results:

  • MGCNSS demonstrated superior performance compared to baseline methods on both balanced and imbalanced datasets.
  • Case studies on colon and esophageal neoplasms validated MGCNSS's capability in identifying potential candidate miRNAs.

Conclusions:

  • MGCNSS offers an effective approach for predicting miRNA-disease associations by leveraging multi-layer graph convolutions and robust negative sampling.
  • The method holds promise for advancing our understanding of disease mechanisms and facilitating the discovery of novel therapeutic targets.