Current annotation strategies for T cell phenotyping of single-cell RNA-seq data

Single-cell RNA sequencing (scRNA-seq) has become a popular technique for interrogating the diversity and dynamic nature of cellular gene expression and has numerous advantages in immunology. For example, scRNA-seq, in contrast to bulk RNA sequencing, can discern cellular subtypes within a populatio...

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Main Authors: Kerry A. Mullan, Nicky de Vrij, Sebastiaan Valkiers, Pieter Meysman
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-12-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fimmu.2023.1306169/full
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author Kerry A. Mullan
Kerry A. Mullan
Nicky de Vrij
Nicky de Vrij
Nicky de Vrij
Sebastiaan Valkiers
Sebastiaan Valkiers
Pieter Meysman
Pieter Meysman
author_facet Kerry A. Mullan
Kerry A. Mullan
Nicky de Vrij
Nicky de Vrij
Nicky de Vrij
Sebastiaan Valkiers
Sebastiaan Valkiers
Pieter Meysman
Pieter Meysman
author_sort Kerry A. Mullan
collection DOAJ
description Single-cell RNA sequencing (scRNA-seq) has become a popular technique for interrogating the diversity and dynamic nature of cellular gene expression and has numerous advantages in immunology. For example, scRNA-seq, in contrast to bulk RNA sequencing, can discern cellular subtypes within a population, which is important for heterogenous populations such as T cells. Moreover, recent advancements in the technology allow the parallel capturing of the highly diverse T-cell receptor (TCR) sequence with the gene expression. However, the field of single-cell RNA sequencing data analysis is still hampered by a lack of gold-standard cell phenotype annotation. This problem is particularly evident in the case of T cells due to the heterogeneity in both their gene expression and their TCR. While current cell phenotype annotation tools can differentiate major cell populations from each other, labelling T-cell subtypes remains problematic. In this review, we identify the common automated strategy for annotating T cells and their subpopulations, and also describe what crucial information is still missing from these tools.
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spelling doaj.art-439db203e2954019b8c376aef48d5e0c2023-12-21T04:15:00ZengFrontiers Media S.A.Frontiers in Immunology1664-32242023-12-011410.3389/fimmu.2023.13061691306169Current annotation strategies for T cell phenotyping of single-cell RNA-seq dataKerry A. Mullan0Kerry A. Mullan1Nicky de Vrij2Nicky de Vrij3Nicky de Vrij4Sebastiaan Valkiers5Sebastiaan Valkiers6Pieter Meysman7Pieter Meysman8Adrem Data Lab, Department of Computer Science, University of Antwerp, Antwerp, BelgiumAntwerp Unit for Data Analysis and Computation in Immunology and Sequencing (AUDACIS) Consortium, University of Antwerp, Antwerp, BelgiumAdrem Data Lab, Department of Computer Science, University of Antwerp, Antwerp, BelgiumAntwerp Unit for Data Analysis and Computation in Immunology and Sequencing (AUDACIS) Consortium, University of Antwerp, Antwerp, BelgiumClinical Immunology Unit, Department of Clinical Sciences, Institute for Tropical Medicine, Antwerp, BelgiumAdrem Data Lab, Department of Computer Science, University of Antwerp, Antwerp, BelgiumAntwerp Unit for Data Analysis and Computation in Immunology and Sequencing (AUDACIS) Consortium, University of Antwerp, Antwerp, BelgiumAdrem Data Lab, Department of Computer Science, University of Antwerp, Antwerp, BelgiumAntwerp Unit for Data Analysis and Computation in Immunology and Sequencing (AUDACIS) Consortium, University of Antwerp, Antwerp, BelgiumSingle-cell RNA sequencing (scRNA-seq) has become a popular technique for interrogating the diversity and dynamic nature of cellular gene expression and has numerous advantages in immunology. For example, scRNA-seq, in contrast to bulk RNA sequencing, can discern cellular subtypes within a population, which is important for heterogenous populations such as T cells. Moreover, recent advancements in the technology allow the parallel capturing of the highly diverse T-cell receptor (TCR) sequence with the gene expression. However, the field of single-cell RNA sequencing data analysis is still hampered by a lack of gold-standard cell phenotype annotation. This problem is particularly evident in the case of T cells due to the heterogeneity in both their gene expression and their TCR. While current cell phenotype annotation tools can differentiate major cell populations from each other, labelling T-cell subtypes remains problematic. In this review, we identify the common automated strategy for annotating T cells and their subpopulations, and also describe what crucial information is still missing from these tools.https://www.frontiersin.org/articles/10.3389/fimmu.2023.1306169/fullT cellssingle cellRNA-seqannotationbioinformaticsadaptive immunity
spellingShingle Kerry A. Mullan
Kerry A. Mullan
Nicky de Vrij
Nicky de Vrij
Nicky de Vrij
Sebastiaan Valkiers
Sebastiaan Valkiers
Pieter Meysman
Pieter Meysman
Current annotation strategies for T cell phenotyping of single-cell RNA-seq data
Frontiers in Immunology
T cells
single cell
RNA-seq
annotation
bioinformatics
adaptive immunity
title Current annotation strategies for T cell phenotyping of single-cell RNA-seq data
title_full Current annotation strategies for T cell phenotyping of single-cell RNA-seq data
title_fullStr Current annotation strategies for T cell phenotyping of single-cell RNA-seq data
title_full_unstemmed Current annotation strategies for T cell phenotyping of single-cell RNA-seq data
title_short Current annotation strategies for T cell phenotyping of single-cell RNA-seq data
title_sort current annotation strategies for t cell phenotyping of single cell rna seq data
topic T cells
single cell
RNA-seq
annotation
bioinformatics
adaptive immunity
url https://www.frontiersin.org/articles/10.3389/fimmu.2023.1306169/full
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