SeqFeatR

SeqFeatR identifies associations between mutation patterns in biological sequences and specific selection pressures to analyze how selection influences genomic variation.


Key Features:

  • Identification of Mutation Patterns: Detects associations between mutation patterns and specific selection pressures in biological sequences.
  • Statistical Methods: Implements both frequentist and Bayesian statistical methods for association analyses.
  • Visualization of Results: Produces visualizations that link statistical outcomes to additional biological properties.
  • Immunological Epitope Discovery: Supports discovery of new T cell epitopes within viral protein sequences for hosts with specific HLA types.

Scientific Applications:

  • Evolutionary Biology: Characterizes how selection pressures shape sequence variation across genomes.
  • Virology: Identifies mutation–feature associations in viral protein sequences.
  • Immunology: Links sequence variation to host HLA-specific immune features, including T cell epitope identification.
  • Vaccine Research: Informs selection of candidate T cell epitopes for vaccine-related studies.

Methodology:

Implemented as an R package that performs statistical association testing between mutation patterns and selection pressures using frequentist and Bayesian approaches and generates visualizations linking statistical results to additional biological properties.

Topics

Details

License:
GPL-3.0
Tool Type:
command-line tool, web application
Operating Systems:
Linux, Windows, Mac
Programming Languages:
R
Added:
10/31/2018
Last Updated:
1/13/2019

Operations

Publications

Budeus B, Timm J, Hoffmann D. SeqFeatR for the Discovery of Feature-Sequence Associations. PLOS ONE. 2016;11(1):e0146409. doi:10.1371/journal.pone.0146409. PMID:26731669. PMCID:PMC4701496.

Documentation

Links