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Related Concept Videos

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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mirMachine: A One-Stop Shop for Plant miRNA Annotation
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Predicting miRNA-disease associations using an ensemble learning framework with resampling method.

Qiguo Dai1,2, Zhaowei Wang1,2, Ziqiang Liu1,2

  • 1School of Computer Science and Engineering, Dalian Minzu University, 116600, Dalian, China.

Briefings in Bioinformatics
|December 20, 2021
PubMed
Summary
This summary is machine-generated.

This study introduces ERMDA, an ensemble learning framework using resampling to predict microRNA (miRNA)-disease associations. ERMDA effectively identifies potential disease-related miRNAs, aiding in understanding complex disease mechanisms.

Keywords:
ensemble learningfeature selectionmiRNA-disease associationresampling

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Area of Science:

  • Genomics
  • Bioinformatics
  • Computational Biology

Background:

  • MicroRNAs (miRNAs) are critical in complex disease pathogenesis.
  • Identifying miRNA-disease associations is vital for disease etiology, diagnosis, and treatment.
  • Experimental methods for miRNA-disease association discovery are resource-intensive.

Purpose of the Study:

  • To develop an effective computational method for predicting miRNA-disease associations.
  • To address the challenge of sample imbalance in miRNA-disease association datasets.
  • To identify novel disease-related miRNAs for further research.

Main Methods:

  • An Ensemble learning framework with Resampling method for MiRNA-Disease Association (ERMDA) prediction was developed.
  • A resampling strategy was employed to create balanced training subsets.
  • Feature representations were extracted by integrating miRNA-miRNA similarities, disease-disease similarities, and known miRNA-disease associations.
  • Feature selection was applied to reduce redundancy and enhance subset diversity.
  • An ensemble approach with soft voting was used for final prediction.

Main Results:

  • ERMDA demonstrated superior performance compared to state-of-the-art methods on both balanced and unbalanced datasets.
  • Case studies on three human diseases validated ERMDA's capability in identifying potential disease-related miRNAs.
  • The method proved effective in exploring the regulatory roles of miRNAs in complex diseases.

Conclusions:

  • ERMDA is an effective and reliable computational tool for predicting miRNA-disease associations.
  • The developed framework aids researchers in uncovering the significance of miRNAs in complex diseases.
  • This approach facilitates the exploration of miRNA functions in disease development and progression.