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MicroRNAs01:22

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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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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...
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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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RNA editing is a post-transcriptional modification where a precursor mRNA (pre-mRNA) nucleotide sequence is changed by base insertion, deletion, or modification. The extent of RNA editing varies from a few hundred bases, in mitochondrial DNA of trypanosomes, to a just single base, in nuclear genes of mammals. Even a single base change in the pre-mRNA can convert a codon for one amino acid into the codon for another amino acid or a stop codon. This type of re-coding can significantly affect the...
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Base complementarity between the three base pairs of mRNA codon and the tRNA anticodon is not a failsafe mechanism. Inaccuracies can range from a single mismatch to no correct base pairing at all. The free energy difference between the correct and nearly correct base pairs can be as small as 3 kcal/ mol. With complementarity being the only proofreading step, the estimated error frequency would be one wrong amino acid in every 100 amino acids incorporated. However, error frequencies observed in...
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Variational graph auto-encoders for miRNA-disease association prediction.

Yulian Ding1, Li-Ping Tian2, Xiujuan Lei3

  • 1Division of Biomedical Engineering, University of Saskatchewan, Saskatoon, SK S7N 5A9, Canada.

Methods (San Diego, Calif.)
|August 18, 2020
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Summary
This summary is machine-generated.

This study introduces VGAE-MDA, a deep learning model for predicting microRNA (miRNA)-disease associations. It accurately identifies relationships, aiding disease understanding and treatment by overcoming limitations of traditional experimental methods.

Keywords:
Deep learningGraph convolutional networkVariational autoencodermiRNA-disease association

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Area of Science:

  • Genomics
  • Computational Biology
  • Biomedical Informatics

Background:

  • MicroRNAs (miRNAs) play crucial roles in biological processes and human diseases.
  • Experimental identification of miRNA-disease associations is costly and time-consuming.
  • Computational methods are needed for efficient prediction of these associations.

Purpose of the Study:

  • To develop an effective deep learning framework for predicting miRNA-disease associations.
  • To improve the accuracy and efficiency of identifying links between miRNAs and diseases.
  • To provide a computational tool for understanding disease mechanisms and potential therapeutic targets.

Main Methods:

  • A deep learning framework utilizing a variational graph auto-encoder (VGAE-MDA) was developed.
  • Heterogeneous networks integrating miRNA-miRNA similarity, disease-disease similarity, and known associations were constructed.
  • Two sub-networks (miRNA-based and disease-based) were created, each employing a VGAE for score calculation.
  • Graph convolutional networks (GCN) and variational autoencoders (VAE) were used to incorporate node features and predict associations from data distribution.

Main Results:

  • VGAE-MDA demonstrated superior performance compared to state-of-the-art methods in miRNA-disease association prediction.
  • The model effectively mitigates noise from negative sample selection.
  • Case studies validated the practical effectiveness of the VGAE-MDA predictions.

Conclusions:

  • VGAE-MDA offers a powerful computational approach for predicting miRNA-disease associations.
  • The framework enhances understanding of disease mechanisms and aids in diagnosis and treatment strategies.
  • This deep learning model represents a significant advancement in the field of computational biology for disease association studies.