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Tumor Dissociation of Highly Viable Cell Suspensions for Single-cell Omic Analyses in Mouse Models of Breast Cancer

Overview
Journal STAR Protoc
Publisher Cell Press
Date 2021 Sep 29
PMID 34585168
Citations 8
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Abstract

Cell preparation with a high rate of viable cells is required to obtain reliable single-cell transcriptomic and epigenomic data. This protocol describes a technique for digestion and single-cell isolation from mouse mammary tumors to achieve ∼90% of viable cells, which can be subsequently processed in a diverse array of high-throughput single-cell "omic platforms," both in an unbiased manner or after selection of a specific cell population. For complete details on the use and execution of this protocol, please refer to Valdes-Mora et al. (2021).

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References
1.
Salomon R, Kaczorowski D, Valdes-Mora F, Nordon R, Neild A, Farbehi N . Droplet-based single cell RNAseq tools: a practical guide. Lab Chip. 2019; 19(10):1706-1727. DOI: 10.1039/c8lc01239c. View

2.
Valdes-Mora F, Salomon R, Gloss B, Law A, Venhuizen J, Castillo L . Single-cell transcriptomics reveals involution mimicry during the specification of the basal breast cancer subtype. Cell Rep. 2021; 35(2):108945. DOI: 10.1016/j.celrep.2021.108945. View