| Literature DB >> 31396939 |
Willem Van Der Byl1,2, Simone Rizzetto1,2, Jerome Samir1,2, Curtis Cai1,2, Auda A Eltahla1,2, Fabio Luciani3,4.
Abstract
Single-cell RNA-seq (scRNA-seq) has provided novel routes to investigate the heterogeneous populations of T cells and is rapidly becoming a common tool for molecular profiling and identification of novel subsets and functions. This chapter offers an experimental and computational workflow for scRNA-seq analysis of T cells. We focus on the analyses of scRNA-seq data derived from plate-based sorted T cells using flow cytometry and full-length transcriptome protocols such as Smart-Seq2. However, the proposed pipeline can be applied to other high-throughput approaches such as UMI-based methods. We describe a detailed bioinformatics pipeline that can be easily reproduced and discuss future directions and current limitations of these methods in the context of T cell biology.Entities:
Keywords: Alignment; Clustering; Differential gene expression; Gene expression matrix; Single-cell RNA sequencing; T cell receptor reconstruction; T cells; scRNA-seq
Mesh:
Year: 2019 PMID: 31396939 DOI: 10.1007/978-1-4939-9728-2_16
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745