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MicroRNAs01:22

MicroRNAs

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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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Bipartite graph-based collaborative matrix factorization method for predicting miRNA-disease associations.

Feng Zhou1, Meng-Meng Yin1, Cui-Na Jiao1

  • 1The School of Computer Science, Qufu Normal University, Rizhao, 276826, China.

BMC Bioinformatics
|November 28, 2021
PubMed
Summary
This summary is machine-generated.

Predicting microRNA-disease associations (MDAs) is crucial for understanding human diseases. A new bipartite graph-based collaborative matrix factorization (BGCMF) method efficiently predicts novel MDAs, achieving high accuracy.

Keywords:
Bipartite graphGaussian interaction profileMatrix factorizationMiRNA–disease associations association prediction

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Area of Science:

  • Biotechnology
  • Genomics
  • Computational Biology

Background:

  • MicroRNAs (miRNAs) are critical in human diseases.
  • Experimental identification of miRNA-disease associations (MDAs) is costly and time-consuming.
  • Computational methods are increasingly used to predict novel MDAs.

Purpose of the Study:

  • To propose an efficient computational method for predicting novel miRNA-disease associations (MDAs).
  • To leverage bipartite graphs and collaborative matrix factorization for improved MDA prediction.

Main Methods:

  • Developed a novel method named bipartite graph-based collaborative matrix factorization (BGCMF).
  • Employed collaborative matrix factorization on a bipartite graph structure.
  • Utilized improved recommendation techniques within the model.

Main Results:

  • The BGCMF method achieved a high Area Under the Curve (AUC) of 0.9514 ± 0.0007 in five-fold cross-validation.
  • The model demonstrated superior performance compared to existing state-of-the-art methods.
  • Successfully predicted numerous potential associations between novel miRNAs and diseases.

Conclusions:

  • The BGCMF method is effective for predicting potential miRNA-disease associations.
  • The high AUC value validates the method's predictive capability.
  • BGCMF offers a valuable tool for advancing research in human diseases by identifying new miRNA roles.