互补DNA
单细胞测序
计算生物学
cDNA文库
生物
信使核糖核酸
协议(科学)
Illumina染料测序
DNA测序
分子生物学
基因
遗传学
医学
外显子组测序
病理
替代医学
突变
作者
Marco De Simone,Grazisa Rossetti,Massimiliano Pagani
出处
期刊:Methods in molecular biology
日期:2019-01-01
卷期号:: 87-110
被引量:9
标识
DOI:10.1007/978-1-4939-9240-9_7
摘要
Chromium 10× 3' V2 protocol is a 3' end counting single-cell mRNA sequencing protocol that allows to process and sequence RNA from thousands of cells in parallel. Chromium10× by 10× Genomics is an emulsion-based device that enables to compartmentalize single cells along with sets of uniquely barcoded primers and reverse transcription reagents into nanoscale droplets that are used as reaction chambers to generate barcoded full-length cDNA from single cells. After RT reaction single-stranded barcoded cDNAs are pooled together and processed to generate sequencing libraries compatible with the standard Illumina platforms. Here we show in detail the main steps of the protocol applied to the analysis of tumor-infiltrating T lymphocytes (TILs). The main steps are cell preparation, cDNA synthesis, library construction, and sequencing.This protocol refers specifically to the CG00052_SingleCell3_ReagentKitv2UserGuide_RevD downloadable from 10× Genomics website ( https://www.10xgenomics.com ) and does not substitute it. Always refer to this guide, paying attention to updates and revisions.
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