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