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SwarmTCR: a computational approach to predict the specificity of T cell receptors

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 neare...

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Autores principales: Ehrlich, Ryan, Kamga, Larisa, Gil, Anna, Luzuriaga, Katherine, Selin, Liisa K., Ghersi, Dario
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8422754/
https://www.ncbi.nlm.nih.gov/pubmed/34493215
http://dx.doi.org/10.1186/s12859-021-04335-w
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author Ehrlich, Ryan
Kamga, Larisa
Gil, Anna
Luzuriaga, Katherine
Selin, Liisa K.
Ghersi, Dario
author_facet Ehrlich, Ryan
Kamga, Larisa
Gil, Anna
Luzuriaga, Katherine
Selin, Liisa K.
Ghersi, Dario
author_sort Ehrlich, Ryan
collection PubMed
description 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). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-021-04335-w.
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spelling pubmed-84227542021-09-09 SwarmTCR: a computational approach to predict the specificity of T cell receptors Ehrlich, Ryan Kamga, Larisa Gil, Anna Luzuriaga, Katherine Selin, Liisa K. Ghersi, Dario BMC Bioinformatics Research 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). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-021-04335-w. BioMed Central 2021-09-07 /pmc/articles/PMC8422754/ /pubmed/34493215 http://dx.doi.org/10.1186/s12859-021-04335-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Ehrlich, Ryan
Kamga, Larisa
Gil, Anna
Luzuriaga, Katherine
Selin, Liisa K.
Ghersi, Dario
SwarmTCR: a computational approach to predict the specificity of T cell receptors
title 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_short 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
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8422754/
https://www.ncbi.nlm.nih.gov/pubmed/34493215
http://dx.doi.org/10.1186/s12859-021-04335-w
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