转录组
表位
计算生物学
生物
单细胞测序
寡核苷酸
细胞
RNA序列
核糖核酸
表型
DNA测序
基因
单细胞分析
遗传学
基因表达
抗体
外显子组测序
作者
Marlon Stoeckius,Christoph Hafemeister,William Stephenson,Brian Houck‐Loomis,Pratip K. Chattopadhyay,Harold Swerdlow,Rahul Satija,Peter Smibert
出处
期刊:Nature Methods
[Springer Nature]
日期:2017-07-31
卷期号:14 (9): 865-868
被引量:2424
摘要
Using established high-throughput single-cell RNA-seq platforms, CITE-seq combines highly multiplexed, antibody-based protein marker quantification with unbiased transcriptome profiling for thousands of single cells. High-throughput single-cell RNA sequencing has transformed our understanding of complex cell populations, but it does not provide phenotypic information such as cell-surface protein levels. Here, we describe cellular indexing of transcriptomes and epitopes by sequencing (CITE-seq), a method in which oligonucleotide-labeled antibodies are used to integrate cellular protein and transcriptome measurements into an efficient, single-cell readout. CITE-seq is compatible with existing single-cell sequencing approaches and scales readily with throughput increases.
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