SwarmTCR: a computational approach to predict the specificity of T cell receptors
Abstract Background With more T cell receptor sequence data becoming available, the need for bioinformatics approaches to predict T cell receptor specificity is even more pressing. Here we present SwarmTCR, a method that uses labeled sequence data to predict the specificity of T cell receptors using...
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doaj-06c2843c05004ca49def50d2919dec522021-09-12T11:13:29ZengBMCBMC Bioinformatics1471-21052021-09-0122111410.1186/s12859-021-04335-wSwarmTCR: a computational approach to predict the specificity of T cell receptorsRyan Ehrlich0Larisa Kamga1Anna Gil2Katherine Luzuriaga3Liisa K. Selin4Dario Ghersi5School of Interdisciplinary Informatics, College of Information Science and Technology, University of Nebraska at OmahaProgram in Molecular Medicine, University of Massachusetts Medical SchoolDepartment of Pathology, University of Massachusetts Medical SchoolProgram in Molecular Medicine, University of Massachusetts Medical SchoolDepartment of Pathology, University of Massachusetts Medical SchoolSchool of Interdisciplinary Informatics, College of Information Science and Technology, University of Nebraska at OmahaAbstract Background With more T cell receptor sequence data becoming available, the need for bioinformatics approaches to predict T cell receptor specificity is even more pressing. Here we present SwarmTCR, a method that uses labeled sequence data to predict the specificity of T cell receptors using a nearest-neighbor approach. SwarmTCR works by optimizing the weights of the individual CDR regions to maximize classification performance. Results We compared the performance of SwarmTCR against another nearest-neighbor method and showed that SwarmTCR performs well both with bulk sequencing data and with single cell data. In addition, we show that the weights returned by SwarmTCR are biologically interpretable. Conclusions Computationally predicting the specificity of T cell receptors can be a powerful tool to shed light on the immune response against infectious diseases and cancers, autoimmunity, cancer immunotherapy, and immunopathology. SwarmTCR is distributed freely under the terms of the GPL-3 license. The source code and all sequencing data are available at GitHub ( https://github.com/thecodingdoc/SwarmTCR ).https://doi.org/10.1186/s12859-021-04335-wTCRImmunoinformaticsBinding specificity |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ryan Ehrlich Larisa Kamga Anna Gil Katherine Luzuriaga Liisa K. Selin Dario Ghersi |
spellingShingle |
Ryan Ehrlich Larisa Kamga Anna Gil Katherine Luzuriaga Liisa K. Selin Dario Ghersi SwarmTCR: a computational approach to predict the specificity of T cell receptors BMC Bioinformatics TCR Immunoinformatics Binding specificity |
author_facet |
Ryan Ehrlich Larisa Kamga Anna Gil Katherine Luzuriaga Liisa K. Selin Dario Ghersi |
author_sort |
Ryan Ehrlich |
title |
SwarmTCR: a computational approach to predict the specificity of T cell receptors |
title_short |
SwarmTCR: a computational approach to predict the specificity of T cell receptors |
title_full |
SwarmTCR: a computational approach to predict the specificity of T cell receptors |
title_fullStr |
SwarmTCR: a computational approach to predict the specificity of T cell receptors |
title_full_unstemmed |
SwarmTCR: a computational approach to predict the specificity of T cell receptors |
title_sort |
swarmtcr: a computational approach to predict the specificity of t cell receptors |
publisher |
BMC |
series |
BMC Bioinformatics |
issn |
1471-2105 |
publishDate |
2021-09-01 |
description |
Abstract Background With more T cell receptor sequence data becoming available, the need for bioinformatics approaches to predict T cell receptor specificity is even more pressing. Here we present SwarmTCR, a method that uses labeled sequence data to predict the specificity of T cell receptors using a nearest-neighbor approach. SwarmTCR works by optimizing the weights of the individual CDR regions to maximize classification performance. Results We compared the performance of SwarmTCR against another nearest-neighbor method and showed that SwarmTCR performs well both with bulk sequencing data and with single cell data. In addition, we show that the weights returned by SwarmTCR are biologically interpretable. Conclusions Computationally predicting the specificity of T cell receptors can be a powerful tool to shed light on the immune response against infectious diseases and cancers, autoimmunity, cancer immunotherapy, and immunopathology. SwarmTCR is distributed freely under the terms of the GPL-3 license. The source code and all sequencing data are available at GitHub ( https://github.com/thecodingdoc/SwarmTCR ). |
topic |
TCR Immunoinformatics Binding specificity |
url |
https://doi.org/10.1186/s12859-021-04335-w |
work_keys_str_mv |
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