JLCRB

JLCRB predicts RNA-binding protein (RBP) binding sites on circular RNAs (circRNAs) using multi-view joint representation learning to integrate and calibrate diverse feature encodings.


Key Features:

  • Multi-View Feature Encoding: Utilizes diverse encoding methods to extract comprehensive RNA-related features from multiple perspectives.
  • Intrinsic Connection Construction: Constructs a global joint representation that captures intrinsic relationships between different view features rather than simple concatenation.
  • Feature Calibration: Calibrates each view's features based on the global joint representation to emphasize critical features and suppress less relevant ones.
  • Depth Feature Fusion: Integrates depth features derived from multiple views and fuses them for accurate detection of RBP binding sites on circRNAs.

Scientific Applications:

  • CircRNA–RBP interaction mapping: Enables identification of RBP binding sites on circRNAs to support studies of RNA–protein interactions.
  • Gene regulation and disease research: Facilitates investigation of circRNA roles in gene regulation and disease mechanisms by providing binding-site information.
  • Performance benchmark: Demonstrated an average Area Under the Curve (AUC) of 93.68% across 37 CircRNA-RBP datasets.

Methodology:

Feature extraction via multiple encoding methods; construction of a global joint representation by integrating multi-view features; calibration of view-specific features using the global joint representation; fusion of depth features for binding site detection.

Topics

Details

License:
Not licensed
Cost:
Free of charge
Tool Type:
command-line tool, web application
Operating Systems:
Mac, Linux, Windows
Programming Languages:
Python
Added:
12/29/2022
Last Updated:
11/24/2024

Operations

Data Inputs & Outputs

Binding site prediction

Inputs

Outputs

    Publications

    Du X, Xue Z. JLCRB: A unified multi-view-based joint representation learning for CircRNA binding sites prediction. Journal of Biomedical Informatics. 2022;136:104231. doi:10.1016/j.jbi.2022.104231. PMID:36309196.

    Links