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Related Concept Videos

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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Predicting LncRNA-Disease Association Based on Generative Adversarial Network.

Biao Du1,2, Lin Tang2, Lin Liu1,2

  • 1School of Information, Yunnan Normal University, Kunming, China.

Current Gene Therapy
|May 17, 2021
PubMed
Summary
This summary is machine-generated.

This study introduces LDA-GAN, a novel computational model for predicting long non-coding RNA (lncRNA)-disease associations. LDA-GAN enhances prediction accuracy and efficiency by leveraging generative adversarial networks and Gumbel-softmax sampling.

Keywords:
Generate adversarial networkLncRNAdiscriminatordiseasegeneratorpairwise loss

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Area of Science:

  • Genomics
  • Bioinformatics
  • Computational Biology

Background:

  • Long non-coding RNAs (lncRNAs) are increasingly recognized for their roles in human diseases.
  • Currently, only a limited number of lncRNA-disease associations are experimentally validated.
  • Computational models are crucial for predicting these associations, reducing experimental costs.

Purpose of the Study:

  • To develop a predictive model for lncRNA-disease associations using limited known data.
  • To propose a novel model, LDA-GAN, based on Generative Adversarial Networks (GANs).

Main Methods:

  • LDA-GAN employs Gumbel-softmax technology for differentiable discrete sampling, addressing GAN limitations.
  • The model integrates generator and discriminator with a pairwise loss function for optimization.
  • Utilizes a semi-supervised learning approach within the GAN framework.

Main Results:

  • LDA-GAN demonstrates high stability and efficiency in adversarial learning.
  • The model significantly improves prediction accuracy for lncRNA-disease associations.
  • Case studies confirm LDA-GAN's ability to identify potential disease associations for lncRNAs.

Conclusions:

  • A generative adversarial model, LDA-GAN, is introduced for identifying lncRNA-disease associations.
  • LDA-GAN offers an effective computational approach to advance understanding of lncRNA roles in disease.