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Pooled CRISPR screening with single-cell transcriptome read-out

CRISPR-based genetic screens are accelerating biological discovery, but current methods have inherent limitations. Widely used pooled screens are restricted to simple readouts including cell proliferation and sortable marker proteins. Arrayed screens allow for comprehensive molecular readouts such a...

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Detalles Bibliográficos
Autores principales: Datlinger, Paul, Rendeiro, André F, Schmidl, Christian, Krausgruber, Thomas, Traxler, Peter, Klughammer, Johanna, Schuster, Linda C, Kuchler, Amelie, Alpar, Donat, Bock, Christoph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5334791/
https://www.ncbi.nlm.nih.gov/pubmed/28099430
http://dx.doi.org/10.1038/nmeth.4177
Descripción
Sumario:CRISPR-based genetic screens are accelerating biological discovery, but current methods have inherent limitations. Widely used pooled screens are restricted to simple readouts including cell proliferation and sortable marker proteins. Arrayed screens allow for comprehensive molecular readouts such as transcriptome profiling, but at much lower throughput. Here we combine pooled CRISPR screening with single-cell RNA sequencing into a broadly applicable workflow, directly linking guide-RNA expression to transcriptome responses in thousands of individual cells. Our method for CRISPR droplet sequencing (CROP-seq) enables pooled CRISPR screens with single-cell transcriptome resolution, which will facilitate high-throughput functional dissection of complex regulatory mechanisms and heterogeneous cell populations.