谱系(遗传)
单细胞分析
计算生物学
人口
克隆(Java方法)
转录组
细胞
转导(生物物理学)
生物
遗传学
DNA
基因表达
基因
生物化学
社会学
人口学
作者
Wenjun Kong,Brent A. Biddy,Kenji Kamimoto,Junedh Amrute,Emily G. Butka,Samantha A. Morris
出处
期刊:Nature Protocols
[Springer Nature]
日期:2020-02-12
卷期号:15 (3): 750-772
被引量:86
标识
DOI:10.1038/s41596-019-0247-2
摘要
Single-cell technologies are offering unparalleled insight into complex biology, revealing the behavior of rare cell populations that are masked in bulk population analyses. One current limitation of single-cell approaches is that lineage relationships are typically lost as a result of cell processing. We recently established a method, CellTagging, permitting the parallel capture of lineage information and cell identity via a combinatorial cell indexing approach. CellTagging integrates with high-throughput single-cell RNA sequencing, where sequential rounds of cell labeling enable the construction of multi-level lineage trees. Here, we provide a detailed protocol to (i) generate complex plasmid and lentivirus CellTag libraries for labeling of cells; (ii) sequentially CellTag cells over the course of a biological process; (iii) profile single-cell transcriptomes via high-throughput droplet-based platforms; and (iv) generate a CellTag expression matrix, followed by clone calling and lineage reconstruction. This lentiviral-labeling approach can be deployed in any organism or in vitro culture system that is amenable to viral transduction to simultaneously profile lineage and identity at single-cell resolution. This protocol describes a lentiviral tagging approach that permits sequential rounds of cell labeling and lineage reconstruction in cells amenable to viral transduction. Transcriptomes and CellTags are captured simultaneously on a droplet-based scRNA-seq platform.
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