Droplet barcoding for massively parallel single-molecule deep sequencing

被引:78
作者
Lan, Freeman [1 ,2 ]
Haliburton, John R. [1 ,3 ]
Yuan, Aaron [1 ,4 ]
Abate, Adam R. [1 ,2 ,3 ,5 ]
机构
[1] Univ Calif San Francisco, Dept Bioengn & Therapeut Sci, Calif Inst Quantitat Biosci QB3, San Francisco, CA 94158 USA
[2] Univ Calif San Francisco, UCSF Bioengn Grad Program, UC Berkeley, San Francisco, CA 94158 USA
[3] Univ Calif San Francisco, Integrat Program Quantitat Biol iPQB Biophys Grad, San Francisco, CA 94158 USA
[4] Univ Calif Berkeley, Dept Elect Engn & Comp Sci EECS, Comp Sci Div CS, Berkeley, CA 94720 USA
[5] Univ Calif San Francisco, Dept Bioengn & Therapeut Sci, 1700 4th St, San Francisco, CA 94158 USA
来源
NATURE COMMUNICATIONS | 2016年 / 7卷
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
GENOME ASSEMBLIES; CANCER GENOMES; DNA; READS; QUANTIFICATION; MICROFLUIDICS; TRANSPOSITION; AMPLIFICATION; LIBRARIES; PARTICLES;
D O I
10.1038/ncomms11784
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The ability to accurately sequence long DNA molecules is important across biology, but existing sequencers are limited in read length and accuracy. Here, we demonstrate a method to leverage short-read sequencing to obtain long and accurate reads. Using droplet microfluidics, we isolate, amplify, fragment and barcode single DNA molecules in aqueous picolitre droplets, allowing the full-length molecules to be sequenced with multi-fold coverage using short-read sequencing. We show that this approach can provide accurate sequences of up to 10 kb, allowing us to identify rare mutations below the detection limit of conventional sequencing and directly link them into haplotypes. This barcoding methodology can be a powerful tool in sequencing heterogeneous populations such as viruses.
引用
收藏
页数:10
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