Scalable microfluidics for single-cell RNA printing and sequencing

被引:92
|
作者
Bose, Sayantan [1 ]
Wan, Zhenmao [2 ]
Carr, Ambrose [2 ]
Rizvi, Abbas H. [3 ]
Vieira, Gregory [1 ]
Pe'er, Dana [1 ,2 ]
Sims, Peter A. [1 ,3 ,4 ]
机构
[1] Columbia Univ, Med Ctr, Dept Syst Biol, New York, NY 10032 USA
[2] Columbia Univ, Dept Biol Sci, New York, NY 10027 USA
[3] Columbia Univ, Med Ctr, Dept Biochem & Mol Biophys, New York, NY 10032 USA
[4] Columbia Univ, Med Ctr, Sulzberger Columbia Genome Ctr, New York, NY 10032 USA
来源
GENOME BIOLOGY | 2015年 / 16卷
基金
美国国家科学基金会;
关键词
POLYMERASE-CHAIN-REACTION; IN-SITU; SEQ; TRANSCRIPTS; MICROREACTORS; HETEROGENEITY; AMPLIFICATION; ARRAYS;
D O I
10.1186/s13059-015-0684-3
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
Many important biological questions demand single-cell transcriptomics on a large scale. Hence, new tools are urgently needed for efficient, inexpensive manipulation of RNA from individual cells. We report a simple platform for trapping single-cell lysates in sealed, picoliter microwells capable of printing RNA on glass or capturing RNA on beads. We then develop a scalable technology for genome-wide, single-cell RNA-Seq. Our device generates pooled libraries from hundreds of individual cells with consumable costs of $0.10 $0.20 per cell and includes five lanes for simultaneous experiments. We anticipate that this system will serve as a general platform for single-cell imaging and sequencing.
引用
收藏
页数:16
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