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Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
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GAERF: predicting lncRNA-disease associations by graph auto-encoder and random forest.

Qing-Wen Wu1, Jun-Feng Xia2, Jian-Cheng Ni3

  • 1Key Lab of Intelligent Computing and Signal Processing of Ministry of Education, College of Computer Science and Technology, Anhui University, Hefei, China.

Briefings in Bioinformatics
|January 8, 2021
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Summary

This study introduces GAERF, a machine learning method using graph auto-encoders and random forests to predict disease-related long non-coding RNAs (lncRNAs) and their associations with diseases.

Keywords:
graph auto-encodergraph convolutional networkgraph embeddinglncRNA-disease associationrandom forest

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Area of Science:

  • Bioinformatics
  • Computational Biology
  • Genomics

Background:

  • Identifying disease-related long non-coding RNAs (lncRNAs) is crucial for developing biomarkers for complex human diseases.
  • Existing methods may face challenges with high-dimensional and heterogeneous biological data.

Purpose of the Study:

  • To propose a novel machine learning approach, GAERF, for accurately identifying disease-related lncRNAs.
  • To predict novel lncRNA-disease associations (LDAs) for improved disease understanding and management.

Main Methods:

  • Constructed a heterogeneous network integrating lncRNA, miRNA, and disease relationships.
  • Employed a graph auto-encoder (GAE) to learn low-dimensional representations of biological entities.
  • Utilized a random forest (RF) classifier, trained on GAE features, to predict LDAs.

Main Results:

  • GAE effectively reduced data dimensionality and heterogeneity, enabling accurate characterization of lncRNA-disease relationships.
  • The GAERF model demonstrated superior performance in predicting LDAs compared to other methods.
  • Ensemble learning within GAERF contributed to its enhanced predictive accuracy.

Conclusions:

  • GAERF is an effective computational method for predicting lncRNA-disease associations.
  • The approach accurately represents lncRNA-disease interactions, aiding in biomarker discovery.
  • Further case studies validated GAERF's utility in identifying potential disease-related lncRNAs.