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lncRNA - Long Non-coding RNAs02:39

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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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A representation learning model based on variational inference and graph autoencoder for predicting lncRNA-disease

Zhuangwei Shi1, Han Zhang2, Chen Jin3

  • 1College of Artificial Intelligence, Nankai University, Tongyan Road, 300350, Tianjin, China.

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|March 22, 2021
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Summary

Predicting long non-coding RNA (lncRNA) and disease associations is vital for healthcare. VGAELDA, a novel deep learning model, accurately identifies these links by learning efficient low-dimensional representations, outperforming existing methods.

Keywords:
Graph autoencoderRepresentation learningVariational inferencelncRNA-disease association

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Area of Science:

  • Bioinformatics
  • Computational Biology
  • Genomics

Background:

  • Long non-coding RNAs (lncRNAs) are implicated in numerous human diseases.
  • Accurate prediction of lncRNA-disease associations is crucial for disease prognosis, diagnosis, and therapy.
  • Existing machine and deep learning methods struggle to learn effective low-dimensional representations from high-dimensional lncRNA and disease data.

Purpose of the Study:

  • To develop an advanced computational model for predicting lncRNA-disease associations.
  • To improve the accuracy and robustness of predicting unknown associations.
  • To address the challenge of learning efficient low-dimensional representations from complex biological data.

Main Methods:

  • Proposed VGAELDA, an end-to-end model integrating variational inference and graph autoencoders.
  • Employed Variational Graph Autoencoders (VGAE) for inferring lncRNA and disease representations.
  • Utilized graph autoencoders for label propagation based on known associations.
  • Implemented an alternating training strategy using the variational expectation-maximization algorithm.

Main Results:

  • VGAELDA effectively captures efficient low-dimensional representations from high-dimensional features.
  • The model demonstrates enhanced robustness and precision in predicting lncRNA-disease associations.
  • VGAELDA addresses a geometric matrix completion problem using a deep learning approach.
  • Cross-validation and numerical experiments confirm superior performance compared to state-of-the-art methods.

Conclusions:

  • VGAELDA significantly outperforms existing methods in lncRNA-disease association prediction.
  • The model successfully identifies potential lncRNA-disease associations through case studies.
  • Source code and data are publicly available for reproducibility and further research.