Ensemble learning can significantly improve human microRNA target prediction
Seunghak Yu1, Juho Kim2, Hyeyoung Min3
1Department of Electrical and Computer Engineering, Seoul National University, Seoul 151-744, Republic of Korea; Department of IT Convergence, Korea University, Seoul 156-713, Republic of Korea.
Methods (San Diego, Calif.)
|August 5, 2014
Summary
We developed SMILE, a novel computational method for predicting microRNA (miRNA) targets. This ensemble learning approach integrates multiple tools to improve accuracy in identifying miRNA-mRNA interactions.
Area of Science:
- Genomics
- Bioinformatics
- Molecular Biology
Background:
- MicroRNAs (miRNAs) are crucial regulators of gene expression involved in numerous biological processes.
- Computational prediction of miRNA targets is essential for biological verification but remains challenging due to tool variability.
- Existing in silico methods often yield conflicting results, highlighting the need for improved prediction accuracy.
Purpose of the Study:
- To develop a novel, robust computational methodology for predicting microRNA (miRNA)-mRNA interactions.
- To enhance the accuracy and reliability of miRNA target prediction by integrating multiple prediction tools.
- To provide a flexible framework for future advancements in understanding in vivo miRNA-mRNA interactions.
Main Methods:
- Proposed a novel target prediction methodology named stacking-based miRNA interaction learner ensemble (SMILE).
- Employed stacked generalization (stacking), an ensemble learning technique, to integrate outputs from individual prediction tools.
- Tested the SMILE method on human miRNA-mRNA interaction data sourced from public databases.
Main Results:
- SMILE significantly improved the accuracy of miRNA target prediction.
- Performance enhancement was measured by the area under the receiver operating characteristic curve (AUC).
- The ensemble approach demonstrated superior predictive power compared to individual tools.
Conclusions:
- SMILE offers a flexible and effective framework for elucidating in vivo miRNA-mRNA interactions.
- The methodology allows for easy incorporation of new target prediction tools as component learners.
- This approach addresses the limitations of existing methods by providing more reliable miRNA target predictions.
Related Concept Videos
MicroRNAs
3.0K
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...
3.0K
MicroRNAs
20.9K
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...
20.9K
MicroRNAs
9.8K
9.8K
Improving Translational Accuracy
11.5K
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...
11.5K
Improving Translational Accuracy
2.6K
2.6K
Human Virome
45
The human body harbors a vast and diverse viral community known as the human virome. The virome includes bacteriophages that infect bacteria, and eukaryotic viruses that infect human cells. Transient dietary and environmental viruses also contribute to this dynamic ecosystem. Estimates suggest the human body may contain on the order of 10¹³ viral particles, though abundance varies widely by body site and detection method.Comprehensive characterization of the virome has become possible...
45


