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lncRNA - Long Non-coding RNAs02:39

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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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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 Knowledge Graph Approach to Elucidate the Role of Organellar Pathways in Disease via Biomedical Reports
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Inferring LncRNA-disease associations based on graph autoencoder matrix completion.

Ximin Wu1, Wei Lan2, Qingfeng Chen1

  • 1School of Computer, Electronic and Information, Guangxi University, Nanning, China.

Computational Biology and Chemistry
|June 6, 2020
PubMed
Summary

This study introduces GAMCLDA, a computational framework using graph autoencoders to predict long non-coding RNA (lncRNA) and disease associations. GAMCLDA effectively identifies these crucial biological links, aiding disease understanding and treatment.

Keywords:
Graph convolutional networkInner productLncRNA-disease associationMatrix completion

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Area of Science:

  • Genomics
  • Computational Biology
  • Bioinformatics

Background:

  • Long non-coding RNAs (lncRNAs) are integral to numerous biological processes.
  • Understanding lncRNA-disease associations is vital for deciphering disease mechanisms and advancing diagnostics and therapeutics.

Purpose of the Study:

  • To develop a novel computational framework, GAMCLDA, for accurate prediction of lncRNA-disease associations.
  • To enhance the understanding of molecular mechanisms underlying human diseases through lncRNA-disease association identification.

Main Methods:

  • Employed a graph autoencoder matrix completion (GAMCLDA) approach.
  • Utilized graph convolutional networks for encoding node features and local graph structures.
  • Integrated a cost-sensitive neural network to address class imbalance in sample data.

Main Results:

  • GAMCLDA demonstrated superior prediction performance compared to existing state-of-the-art methods.
  • Evaluated performance using AUC, AUPR, PPV, and F1-score metrics.
  • Case studies confirmed GAMCLDA's efficacy in predicting potential lncRNA-disease relationships.

Conclusions:

  • GAMCLDA provides an effective computational tool for identifying lncRNA-disease associations.
  • The framework aids in understanding disease pathogenesis and offers potential for clinical applications.
  • Accurate prediction of these associations is crucial for future biomedical research and development.