核糖核酸
转录组
流式细胞术
细胞
寡核苷酸
生物
计算生物学
分子生物学
基因表达
基因
遗传学
作者
Valentina Russo,Nadia Brasu,Luigia Pace
标识
DOI:10.1007/978-1-0716-1771-7_16
摘要
Single-cell RNA sequencing (sc-RNAseq) has become a critical approach for the analysis of immune cell function and heterogeneity. So far, the immune cell isolation, based on surface marker expression predicted by the RNA expression profiles, is often limited by the poor correlation between transcript and protein expression patterns. To overcome these difficulties, novel single-cell multi-omic approaches based on the combined analysis of transcript and surface protein expression have been developed. One of the major benefits of these technologies is the possibility to use a high number of antibodies conjugated with oligonucleotide (AbOs) for the surface marker detection, thus overcoming the limit of using few surface markers as occurs in flow cytometry. Here we describe the BD Rhapsody single-cell analysis system protocol for 3′ mRNA whole transcriptome analysis (WTA), combined with AbO- and Sample Tag library preparation.
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