PRR-HyPred

PRR-HyPred predicts and classifies pattern recognition receptors (PRRs) into specific PRR families to support functional characterization and studies of innate immunity.


Key Features:

  • Two-layer hybrid framework: A first-layer support vector machine (SVM) discriminates PRR versus non-PRR sequences.
  • Family classification: A second-layer random forest classifier assigns predicted PRRs to families including Toll-like receptors, retinoic acid-inducible gene-I-like receptors, nucleotide oligomerization domain-like receptors, and C-type lectin receptors.
  • Sequence-encoded optimal features: Predictions use sequence-encoded optimal features extracted from input sequences as machine-learning input.
  • Performance metrics: Reported 10-fold cross-validation performance: layer 1 accuracy 83.4% and Matthew's correlation coefficient 0.639; layer 2 accuracy 95% and Matthew's correlation coefficient 0.816.

Scientific Applications:

  • Innate immunity research: Enables large-scale identification and cataloging of PRRs relevant to innate immune recognition.
  • Functional characterization: Supports assignment of PRR sequences to specific families for downstream functional inference.
  • Therapeutic and disease research: Facilitates discovery of PRR-related targets and investigation of mechanisms in immunology and disease.

Methodology:

Sequence-encoded optimal features are used as input to a two-layer machine-learning pipeline comprising a support vector machine for PRR/non-PRR discrimination and a random forest classifier for family assignment, with performance assessed by 10-fold cross-validation.

Topics

Details

Cost:
Free of charge
Tool Type:
web application
Operating Systems:
Mac, Linux, Windows
Added:
3/18/2023
Last Updated:
11/24/2024

Operations

Publications

Firoz A, Malik A, Ali HM, Akhter Y, Manavalan B, Kim C. PRR-HyPred: A two-layer hybrid framework to predict pattern recognition receptors and their families by employing sequence encoded optimal features. International Journal of Biological Macromolecules. 2023;234:123622. doi:10.1016/j.ijbiomac.2023.123622. PMID:36773859.

PMID: 36773859
Funding: - King Abdulaziz University: D-210-130-1440