cDNA文库
生物
互补DNA
转录组
计算生物学
核糖核酸
RNA序列
免疫系统
细胞
基因组文库
分子生物学
基因
遗传学
基因表达
基序列
出处
期刊:Methods in molecular biology
日期:2020-01-01
卷期号:: 1-18
被引量:1
标识
DOI:10.1007/978-1-0716-0802-9_1
摘要
Single-cell RNA-sequencing (scRNA-seq) enables a comprehensive analysis of the transcriptome of individual cells by next-generation sequencing. ScRNA-seq offers an unbiased approach to investigate the cellular heterogeneity and dynamics of diverse biological systems, including the immune system. Optimization of the technical procedures performed prior to RNA-seq analysis is imperative to the success of a scRNA-seq experiment. Here, three major experimental procedures are described: (1) the isolation of immune CD8a+ T cells from primary murine tissue, (2) the generation of single-cell cDNA libraries using the 10× Genomics Chromium Controller and the Chromium Single Cell 3′ Solution, and (3) cDNA library quality control. In this protocol, CD8a+ T cells are isolated from murine spleen tissue, but any cell type of interest can be enriched and used for single-cell cDNA library generation and subsequent RNA-seq experiments.
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