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Current annotation strategies for T cell phenotyping of single-cell RNA-seq data
Tijdschriftbijdrage - Review Artikel
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.
Tijdschrift: Front Immunol
ISSN: 1664-3224
Volume: 14
Jaar van publicatie:2023
Trefwoorden:RNA-seq, T cells, T-cell receptor, Adaptive immunity, Annotation, Bioinformatics, Single cell
Toegankelijkheid:Open