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Flexible Distance-Based TCR Analysis in Python with tcrdist3.

Koshlan Mayer-Blackwell1, Andrew Fiore-Gartland1, Paul G Thomas2

  • 1Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.

Methods in Molecular Biology (Clifton, N.J.)
|September 10, 2022
PubMed
Summary
This summary is machine-generated.

This study introduces tcrdist3, a Python package for analyzing T cell receptor (TCR) sequences. It helps identify antigen-specific TCRs and understand immune responses by analyzing sequence similarities and network features.

Keywords:
BioinformaticsDistance-based learningEpitope-specificityPythonT cell receptorsTCR

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Area of Science:

  • Immunology
  • Bioinformatics
  • Computational Biology

Background:

  • T cell receptor (TCR) sequencing is crucial for studying adaptive immunity.
  • Antigen-specific TCRs often share sequence motifs, indicating functional relationships.

Purpose of the Study:

  • To introduce tcrdist3, a novel Python package for distance-based TCR analysis.
  • To demonstrate tcrdist3's utility in identifying antigen-specific TCRs and analyzing immune repertoires.

Main Methods:

  • Utilizing sequence similarity networks, gene-usage plots, and CDR3 logos for TCR analysis.
  • Employing the TCRjoin feature for querying TCR sequences against large datasets.
  • Leveraging the TCRdist metric for neighbor enrichment testing to identify antigenically selected TCRs.

Main Results:

  • Demonstrated identification of TCR sequence features associated with antigen specificity.
  • Showcased flexible querying of TCR sequences against bulk repertoires.
  • Illustrated identification of candidate polyclonal TCRs under antigenic selection.

Conclusions:

  • tcrdist3 offers a flexible and powerful framework for distance-based TCR analysis.
  • The package facilitates the identification of antigen-specific TCRs and the study of immune responses.
  • tcrdist3 enhances the analysis of TCR repertoire data for immunological research.