Microfluidics as a Strategic Player to Decipher Single-Cell Omics?

被引:18
作者
Caen, Ouriel [1 ]
Lu, Heng [1 ]
Nizard, Philippe [1 ]
Taly, Valerie [1 ]
机构
[1] Paris Descartes Univ, CNRS SNC5014, INSERM UMR S1147, Equipe Labellisee Ligue Natl Canc, Paris, France
关键词
DROPLET-BASED MICROFLUIDICS; WHOLE-GENOME AMPLIFICATION; LARGE-SCALE INTEGRATION; HIGH-THROUGHPUT; RNA-SEQ; MULTIPARAMETER ANALYSIS; SIGNALING PATHWAYS; NANOLITER DROPLETS; DRUG DISCOVERY; TUMOR-CELLS;
D O I
10.1016/j.tibtech.2017.05.004
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
Most cell studies are performed at a population level, relying on the assumption of a normal distribution of the function and fate of a cell among a population. However, technologies allowing single-cell analysis (SCA) have recently arisen and have led to increasing evidence of cell population heterogeneity and its importance. Tremendous amounts of new data could now be uncovered to redefine our understanding of cell omics. Microfluidics has emerged as a major technological player in this new era and is gradually increasing in use among biology laboratories, mainly due to the single-cell high-throughput handling solutions it offers. In this review, we assess its use and relevance for omics analysis at the single-cell level, with a specific focus on compartment-based microfluidic approaches.
引用
收藏
页码:713 / 727
页数:15
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