SecretSanta

SecretSanta predicts extracellular proteins secreted via classical pathways by identifying N-terminal signal peptides and integrating multiple prediction tools for secretome analysis.


Key Features:

  • Integration of Established Tools: Wraps and parses command-line tools with wrapper and parser functions to produce integrative predictions of extracellular proteins secreted via classical pathways.
  • Classical Secretory Pathway Prediction: Detects N-terminal signal peptides to identify proteins routed through the classical secretory pathway.
  • Modularity and Flexibility: Modular design enables construction of customized pipelines and comparative analyses across species or experimental conditions.
  • Scalability and Efficiency: Implemented in the R programming language with parallelized functions optimized for large-scale sequence processing.

Scientific Applications:

  • Biomarker Discovery: Predicts extracellular proteins based on N-terminal signal peptides to identify candidate biomarkers for disease classification.
  • Host-Pathogen Interaction Studies: Analyzes secretomes to support investigation of molecular interactions between hosts and pathogens and related immune responses.
  • Comparative Secretome Analysis: Enables comparison of secretomes across species or environmental conditions to study evolutionary processes and functional adaptations.

Methodology:

Integrates command-line prediction tools via wrapper and parser functions; implemented in R with parallelized functions; predicts secreted proteins by detecting N-terminal signal peptides indicative of the classical secretory pathway.

Topics

Details

Tool Type:
command-line tool
Operating Systems:
Linux, Mac
Programming Languages:
R
Added:
6/30/2018
Last Updated:
11/25/2024

Operations

Publications

Gogleva A, Drost H, Schornack S. SecretSanta: flexible pipelines for functional secretome prediction. Bioinformatics. 2018;34(13):2295-2296. doi:10.1093/bioinformatics/bty088. PMID:29462238. PMCID:PMC6022548.

PMID: 29462238
PMCID: PMC6022548
Funding: - Gatsby Charitable Foundation: RG62472 - Royal Society: RG69135 - European Research Council: 637537, ERC-2014-STG, H2020

Documentation