Microfluidics for single-cell genetic analysis

被引:48
|
作者
Thompson, A. M. [1 ]
Paguirigan, A. L. [2 ]
Kreutz, J. E. [1 ]
Radich, J. P. [2 ]
Chiu, D. T. [1 ]
机构
[1] Univ Washington, Dept Chem, Seattle, WA 98195 USA
[2] Fred Hutchinson Canc Res Ctr, Div Clin Res, Seattle, WA 98104 USA
基金
美国国家卫生研究院;
关键词
SELF-DIGITIZATION; EXPRESSION; ENCAPSULATION; PROGRESSION; DIVERSITY; EVOLUTION;
D O I
10.1039/c4lc00175c
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The ability to correlate single-cell genetic information to cellular phenotypes will provide the kind of detailed insight into human physiology and disease pathways that is not possible to infer from bulk cell analysis. Microfluidic technologies are attractive for single-cell manipulation due to precise handling and low risk of contamination. Additionally, microfluidic single-cell techniques can allow for high-throughput and detailed genetic analyses that increase accuracy and decrease reagent cost compared to bulk techniques. Incorporating these microfluidic platforms into research and clinical laboratory workflows can fill an unmet need in biology, delivering the highly accurate, highly informative data necessary to develop new therapies and monitor patient outcomes. In this perspective, we describe the current and potential future uses of microfluidics at all stages of single-cell genetic analysis, including cell enrichment and capture, single-cell compartmentalization and manipulation, and detection and analyses.
引用
收藏
页码:3135 / 3142
页数:8
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