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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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SGAEMDA: Predicting miRNA-Disease Associations Based on Stacked Graph Autoencoder.

Shudong Wang1, Boyang Lin1, Yuanyuan Zhang1,2

  • 1College of Computer Science and Technology, Qingdao Institute of Software, China University of Petroleum, Qingdao 266580, China.

Cells
|December 23, 2022
PubMed
Summary
This summary is machine-generated.

Predicting microRNA-disease associations (MDA) is vital for healthcare. A new Stacked Graph Autoencoder-Based Prediction of Potential miRNA-Disease Associations (SGAEMDA) model offers a more efficient and accurate approach than traditional methods.

Keywords:
association predictiondiseasehigher-order featuresmiRNAstacked graph autoencoder

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Area of Science:

  • Bioinformatics
  • Computational Biology
  • Genomics

Background:

  • MicroRNA-disease association (MDA) prediction is crucial for disease management.
  • Traditional experimental methods for MDA prediction are time-consuming and expensive.

Purpose of the Study:

  • To develop an efficient computational model for predicting potential miRNA-disease associations.
  • To overcome the limitations of traditional experimental approaches in MDA prediction.

Main Methods:

  • Proposed SGAEMDA (Stacked Graph Autoencoder-Based Prediction of Potential miRNA-Disease Associations), a multi-layer collaborative unsupervised training model.
  • Extracted similarity and association features from miRNA and disease data.
  • Utilized stacked graph autoencoder for unsupervised learning of low-dimensional representations.
  • Integrated learned representations with association features for final pair feature extraction.
  • Employed a multilayer perceptron (MLP) for predicting unknown miRNA-disease associations.

Main Results:

  • SGAEMDA achieved high performance with mean ROC AUC scores of 0.9585 (5-fold CV) and 0.9516 (10-fold CV).
  • The model significantly outperformed existing baseline methods in MDA prediction accuracy.
  • Case studies demonstrated SGAEMDA's ability to accurately identify candidate microRNAs for various neoplasms.

Conclusions:

  • SGAEMDA provides an effective and accurate computational approach for predicting miRNA-disease associations.
  • The model's unsupervised learning capability and feature integration enhance prediction performance.
  • SGAEMDA holds promise for advancing disease prevention, diagnosis, and treatment strategies.