Single-Cell Toolkits Opening a New Era for Cell Engineering

被引:14
作者
Lee, Sean [1 ]
Kim, Jireh [1 ]
Park, Jong-Eun [1 ]
机构
[1] Korea Adv Inst Sci & Technol KAIST, Grad Sch Med Sci & Engn, Daejeon 34141, South Korea
关键词
cell engineering; CRISPR screening; lineage tracing; single-cell multi-omics; RNA-SEQ; CHROMATIN ACCESSIBILITY; TRANSCRIPTOME; PROTEINS; CIRCUITS; LINEAGE;
D O I
10.14348/molcells.2021.0002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Since the introduction of RNA sequencing (RNA-seq) as a high-throughput mRNA expression analysis tool, this procedure has been increasingly implemented to identify cell -level transcriptome changes in a myriad of model systems. However, early methods processed cell samples in bulk, and therefore the unique transcriptomic patterns of individual cells would be lost due to data averaging. Nonetheless, the recent and continuous development of new single-cell RNA sequencing (scRNA-seq) toolkits has enabled researchers to compare transcriptomes at a single-cell resolution, thus facilitating the analysis of individual cellular features and a deeper understanding of cellular functions. Nonetheless, the rapid evolution of high throughput single-cell ?omics? tools has created the need for effective hypothesis verification strategies. Particularly, this issue could be addressed by coupling cell engineering techniques with single-cell sequencing. This approach has been successfully employed to gain further insights into disease pathogenesis and the dynamics of differentiation trajectories. Therefore, this review will discuss the current status of cell engineering toolkits and their contributions to single-cell and genome-wide data collection and analyses.
引用
收藏
页码:127 / 135
页数:9
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