Related Experiment Video
Updated: Nov 6, 2025

06:34
A Bioinformatics Pipeline to Accurately and Efficiently Analyze the MicroRNA Transcriptomes in Plants
Published on: January 21, 2020
8.6K
High precision in microRNA prediction: A novel genome-wide approach with convolutional deep residual networks
C Yones1, J Raad1, L A Bugnon1
1Research Institute for Signals, Systems and Computational Intelligence, sinc(i), FICH-UNL, CONICET, Ciudad Universitaria UNL, 3000, Santa Fe, Argentina.
Computers in Biology and Medicine
|May 12, 2021
Summary
This study introduces mirDNN, a novel deep learning model for predicting microRNA precursors (pre-miRNAs). mirDNN significantly improves prediction accuracy compared to existing methods, even in real-world conditions.
Area of Science:
- Genomics
- Bioinformatics
- Computational Biology
Background:
- MicroRNAs (miRNAs) are crucial regulators of gene expression.
- Accurate computational prediction of miRNA precursors (pre-miRNAs) is essential.
- Existing homology-based and machine learning methods have limitations in precision and handling secondary structures.
Purpose of the Study:
- To develop a novel computational approach for precise pre-miRNA prediction.
- To address the limitations of existing methods, particularly in real-world genomic data.
- To improve the accuracy and reliability of identifying novel miRNA candidates.
Main Methods:
- Development of a convolutional deep residual neural network named mirDNN.
- Testing mirDNN on full genomes of various animal and plant species.
- Implementation of a novel validation methodology for assessing performance on new species.
Main Results:
- mirDNN achieved up to 5 times higher precision than other approaches at similar recall rates.
- The model demonstrated robust performance across diverse animal and plant genomes.
- The novel validation methodology confirmed the practical applicability of mirDNN.
Conclusions:
- mirDNN offers a significant advancement in the computational prediction of pre-miRNAs.
- The approach overcomes limitations of traditional methods by considering secondary structures and improving robustness.
- A web demo and source code are available for accessibility and further research.
More Related Videos
Related Concept Videos
MicroRNAs
3.3K
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...
3.3K
MicroRNAs
22.7K
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...
22.7K
Improving Translational Accuracy
12.1K
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...
12.1K
Improving Translational Accuracy
3.2K
3.2K
CRISPR and crRNAs
18.0K
Bacteria and archaea are susceptible to viral infections just like eukaryotes; therefore, they have developed a unique adaptive immune system to protect themselves. Clustered regularly interspaced short palindromic repeats and CRISPR-associated proteins (CRISPR-Cas) are present in more than 45% of known bacteria and 90% of known archaea.
The CRISPR-Cas system stores a copy of foreign DNA in the host genome and uses it to identify the foreign DNA upon reinfection. CRISPR-Cas has three different...
The CRISPR-Cas system stores a copy of foreign DNA in the host genome and uses it to identify the foreign DNA upon reinfection. CRISPR-Cas has three different...
18.0K

