CellTag Indexing: genetic barcode-based sample multiplexing for single-cell genomics

被引:55
作者
Guo, Chuner [1 ,2 ,3 ]
Kong, Wenjun [1 ,2 ,3 ]
Kamimoto, Kenji [1 ,2 ,3 ]
Rivera-Gonzalez, Guillermo C. [1 ,2 ,3 ]
Yang, Xue [1 ,2 ,3 ]
Kirita, Yuhei [2 ,4 ]
Morris, Samantha A. [1 ,2 ,3 ]
机构
[1] Washington Univ, Dept Dev Biol, Sch Med St Louis, 660 S Euclid Ave,Campus Box 8103, St Louis, MO 63110 USA
[2] Washington Univ, Dept Genet, Sch Med St Louis, 660 S Euclid Ave,Campus Box 8103, St Louis, MO 63110 USA
[3] Washington Univ, Ctr Regenerat Med, Sch Med St Louis, 660 S Euclid Ave,Campus Box 8103, St Louis, MO 63110 USA
[4] Washington Univ, Div Nephrol, Dept Med, Sch Med St Louis, 660 S Euclid Ave,Campus Box 8103, St Louis, MO 63110 USA
基金
美国国家卫生研究院; 日本学术振兴会;
关键词
STEM-CELLS; NEGATIVE REGULATOR; EXPRESSION; LRIG1; MARKER; IDENTITY; FATE; CONVERSION; LINEAGES; CIRCUITS;
D O I
10.1186/s13059-019-1699-y
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
High-throughput single-cell assays increasingly require special consideration in experimental design, sample multiplexing, batch effect removal, and data interpretation. Here, we describe a lentiviral barcode-based multiplexing approach, CellTag Indexing, which uses predefined genetic barcodes that are heritable, enabling cell populations to be tagged, pooled, and tracked over time in the same experimental replicate. We demonstrate the utility of CellTag Indexing by sequencing transcriptomes using a variety of cell types, including long-term tracking of cell engraftment and differentiation in vivo. Together, this presents CellTag Indexing as a broadly applicable genetic multiplexing tool that is complementary with existing single-cell technologies.
引用
收藏
页数:13
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