协议(科学)
RNA序列
计算机科学
计算生物学
质量(理念)
生物
医学
病理
遗传学
转录组
物理
基因表达
基因
量子力学
替代医学
作者
Hiroki Ikeda,Shintaro Miyao,Nobuhiro Yamada,Sumire Sugimoto,Fuminori Kimura,Kazuki Kurimoto
出处
期刊:STAR protocols
[Elsevier]
日期:2024-05-02
卷期号:5 (2): 103050-103050
标识
DOI:10.1016/j.xpro.2024.103050
摘要
Single-cell RNA sequencing (scRNA-seq) combined with laser capture microdissection (LCM) offers a versatile framework for comprehensive transcriptomics from tissue sections. Here, we present a detailed protocol for DRaqL (direct RNA recovery and quenching for LCM) in combination with Smart-seq2 (DRaqL-Smart-seq2), which enables high-quality RNA sequencing for single cells obtained from alcohol-fixed murine ovarian sections. Additionally, we provide an optional procedure for scRNA-seq from formalin-fixed sections (DRaqL-Protease-Smart-seq2). We outline key steps for cell lysis, cDNA amplification, and sequencing library preparation. For complete details on the use and execution of this protocol, please refer to Ikeda et al.1
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