Department of Cell and Molecular Biology, Karolinska Institutet, Stockholm, Sweden.
Nat Biotechnol. 2022 Oct;40(10):1452-1457. doi: 10.1038/s41587-022-01311-4. Epub 2022 May 30.
Current single-cell RNA sequencing (scRNA-seq) methods with high cellular throughputs sacrifice full-transcript coverage and often sensitivity. Here we describe Smart-seq3xpress, which miniaturizes and streamlines the Smart-seq3 protocol to substantially reduce reagent use and increase cellular throughput. Smart-seq3xpress analysis of peripheral blood mononuclear cells resulted in a granular atlas complete with common and rare cell types. Compared with droplet-based single-cell RNA sequencing that sequences RNA ends, the additional full-transcript coverage revealed cell-type-associated isoform variation.
目前具有高通量的单细胞 RNA 测序 (scRNA-seq) 方法牺牲了全长转录本的覆盖度,而且通常也牺牲了灵敏度。在此,我们描述了 Smart-seq3xpress,它将 Smart-seq3 方案小型化和简化,从而大大减少试剂的使用并增加细胞的吞吐量。对外周血单核细胞的 Smart-seq3xpress 分析产生了一个完整的颗粒图谱,其中包括常见和罕见的细胞类型。与基于液滴的单细胞 RNA 测序(仅对 RNA 末端进行测序)相比,额外的全长转录本覆盖度揭示了与细胞类型相关的异构体变异。