ReCGBM
ReCGBM predicts human Dicer cleavage sites in pre-miRNAs to support analysis of microRNA biogenesis and gene regulation.
Key Features:
- Prediction target: Predicts cleavage sites of human Dicer on precursor microRNAs (pre-miRNAs).
- Algorithm: Implements gradient boosting using the lightGBM algorithm.
- Feature types: Incorporates relational and class features derived from input sequences.
- Relational feature design: Uses specifically designed features that capture interactions between different sequences.
- Interpretability: Provides feature importance analysis to identify influential sequence characteristics.
- Central-region emphasis: Highlights the significant contribution of features located near the center of pre-miRNA molecules.
- Benchmarking: Demonstrates improved prediction accuracy relative to PHDCleav and LBSizeCleav in computational experiments.
Scientific Applications:
- RNA processing studies: Supports investigation of Dicer cleavage specificity and mechanisms of pre-miRNA processing.
- Gene regulation research: Aids studies of microRNA biogenesis and its effects on post-transcriptional gene regulation.
- Model development: Guides development of predictive models by identifying informative sequence features, especially near pre-miRNA centers.
Methodology:
Uses gradient boosting with lightGBM, engineered relational and class features that capture inter-sequence interactions, feature importance analysis for interpretability, and computational benchmarking against PHDCleav and LBSizeCleav.
Topics
Details
- Tool Type:
- command-line tool
- Programming Languages:
- Python
- Added:
- 3/19/2021
- Last Updated:
- 4/2/2021
Operations
Publications
Liu P, Song J, Lin C, Akutsu T. ReCGBM: a gradient boosting-based method for predicting human dicer cleavage sites. BMC Bioinformatics. 2021;22(1). doi:10.1186/s12859-021-03993-0. PMID:33568063. PMCID:PMC7877110.
PMID: 33568063
PMCID: PMC7877110
Funding: - Japan Society for the Promotion of Science: 18H04113
- Ministry of Science and Technology, Taiwan: 108-2636-B-009-005
- Institute for Chemical Research, Kyoto University: 2020-25