@article {26,
	title = {Simultaneous epitope and transcriptome measurement in single cells.},
	journal = {Nat Methods},
	volume = {14},
	year = {2017},
	month = {2017 Sep},
	pages = {865-868},
	abstract = {<p>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.</p>},
	keywords = {Epitope Mapping, Epitopes, Gene Expression Profiling, High-Throughput Nucleotide Sequencing, Sequence Analysis, RNA, Tissue Array Analysis, Transcriptome},
	issn = {1548-7105},
	doi = {10.1038/nmeth.4380},
	author = {Stoeckius, Marlon and Hafemeister, Christoph and Stephenson, William and Houck-Loomis, Brian and Chattopadhyay, Pratip K and Swerdlow, Harold and Satija, Rahul and Smibert, Peter}
}
