MBSTAR

MBSTAR predicts functional microRNA (miRNA) binding sites in target mRNA 3' untranslated regions (3' UTRs) to distinguish functional from non-functional potential binding sites.


Key Features:

  • Multiple instance learning: Applies multiple instance learning to manage uncertainty about the exact locations of true miRNA binding sites on target mRNAs.
  • Training data (Tarbase 6.0): Trains on 9531 interacting miRNA–mRNA pairs and 973 non-interacting pairs derived from Tarbase 6.0.
  • PAR-CLIP confirmation: Uses PAR-CLIP dataset overlap to confirm predicted binding sites.
  • Functional-site prioritization: Distinguishes functional versus non-functional potential binding sites to reduce false positives in miRNA target prediction.
  • Performance metric: Demonstrates prediction performance with a maximum F-Score of 0.337 and high overlap with PAR-CLIP validated sites.

Scientific Applications:

  • Functional binding-site identification: Identification of functional miRNA binding sites in 3' UTRs for downstream analyses.
  • Prioritization for experimental validation: Prioritizes candidate sites that overlap PAR-CLIP evidence for more reliable experimental follow-up.
  • Genome-wide target analysis: Enables genome-wide assessment of putative functional miRNA–mRNA interactions.
  • miRNA-mediated regulation studies: Supports investigation of gene regulation mechanisms mediated by miRNAs.

Methodology:

MBSTAR employs multiple instance learning trained on Tarbase 6.0 (9531 interacting pairs and 973 non-interacting pairs) and confirms predictions using PAR-CLIP overlap, with performance evaluated by overlap metrics and F-Score (maximum 0.337).

Topics

Details

Tool Type:
web application
Operating Systems:
Linux, Windows, Mac
Added:
8/3/2017
Last Updated:
11/25/2024

Operations

Publications

Bandyopadhyay S, Ghosh D, Mitra R, Zhao Z. MBSTAR: multiple instance learning for predicting specific functional binding sites in microRNA targets. Scientific Reports. 2015;5(1). doi:10.1038/srep08004. PMID:25614300. PMCID:PMC4648438.

Documentation

Links