Multiplexed detection of proteins, transcriptomes, clonotypes and CRISPR perturbations in single cells.

Multiplexed detection of proteins, transcriptomes, clonotypes and CRISPR perturbations in single cells.

Mimitou, Eleni P;Cheng, Anthony;Montalbano, Antonino;Hao, Stephanie;Stoeckius, Marlon;Legut, Mateusz;Roush, Timothy;Herrera, Alberto;Papalexi, Efthymia;Ouyang, Zhengqing;Satija, Rahul;Sanjana, Neville E;Koralov, Sergei B;Smibert, Peter;
Nature Methods 2019 Vol. 16 pp. 409-412
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mimitou2019multiplexednature

Abstract

Multimodal single-cell assays provide high-resolution snapshots of complex cell populations, but are mostly limited to transcriptome plus an additional modality. Here, we describe expanded CRISPR-compatible cellular indexing of transcriptomes and epitopes by sequencing (ECCITE-seq) for the high-throughput characterization of at least five modalities of information from each single cell. We demonstrate application of ECCITE-seq to multimodal CRISPR screens with robust direct single-guide RNA capture and to clonotype-aware multimodal phenotyping of cancer samples.

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