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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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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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Updated: Sep 14, 2025

mirMachine: A One-Stop Shop for Plant miRNA Annotation
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Using deep neural networks and LASSO regression to predict miRNA expression changes based on mRNA data.

Franz Leonard Böge1, Helena U Zacharias2, Stefanie C Becker3

  • 1Institute for Animal Genomics, University of Veterinary Medicine Hannover Foundation, Hannover, Germany.

Frontiers in Bioinformatics
|July 23, 2025
PubMed
Summary
This summary is machine-generated.

Predicting microRNA (miRNA) expression from mRNA data is feasible using deep learning and LASSO regression. This cross-omics approach shows promise for disease research, even with variations in differential expression analysis.

Keywords:
LASSO regularizationWest Nile virusartificial neural networkshuman immunodeficiency virusmicroRNAmulti-omics

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Area of Science:

  • Multi-omics data analysis in disease research.
  • Computational biology and bioinformatics.
  • Gene expression profiling.

Background:

  • Understanding microRNA (miRNA) and messenger RNA (mRNA) interplay is crucial for disease molecular studies.
  • Paired miRNA/mRNA expression datasets are scarce, limiting integrated analysis.
  • Existing miRNA-target relationship research relies on databases with experimental and computational data.

Purpose of the Study:

  • To assess the feasibility of predicting miRNA expression profiles from mRNA expression data.
  • To demonstrate the potential of cross-omics prediction as a proof of principle.
  • To leverage publicly available mRNA data for miRNA expression inference.

Main Methods:

  • Utilized artificial deep neural networks and LASSO regression for miRNA expression prediction.
  • Evaluated models on seven paired miRNA/mRNA datasets from West Nile virus and HIV infections.
  • Performed within-data and cross-study evaluations, exploring data augmentation and separate models for diseased/non-diseased samples.

Main Results:

  • Achieved strong correlations at the individual sample level across most settings.
  • Observed correlations in log-fold changes and p-values from differential expression analysis (DEA) in some datasets.
  • Data augmentation consistently improved neural network performance, with less impact on LASSO models.

Conclusions:

  • Cross-omics prediction of miRNA expression from mRNA data is demonstrated as feasible.
  • The approach shows potential for inferring miRNA profiles where paired data is unavailable.
  • Correlations in differential expression analysis suggest the utility of this method in disease research.