Sequence specific sorting of DNA molecules with FACS using 3dPCR

被引:26
作者
Sukovich, David J. [1 ,2 ]
Lance, Shea T. [1 ,2 ,3 ]
Abate, Adam R. [1 ,2 ,3 ]
机构
[1] Univ Calif San Francisco, Bioengn & Therapeut Sci, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Calif Inst Quantitat Biosci, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, UC Berkeley UCSF Grad Program Bioengn, San Francisco, CA 94143 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
DIGITAL PCR; ENRICHMENT; EVOLUTION; BACTERIAL; PLASMA; WATER;
D O I
10.1038/srep39385
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
Genetic heterogeneity is an important feature of many biological systems, but introduces technical challenges to their characterization. Even with the best modern instruments, only a small fraction of DNA molecules present in a sample can be read, and they are recovered in the form of short, hundred-base reads. In this paper, we introduce 3dPCR, a method to sort DNA molecules with sequence specificity. 3dPCR allows heterogeneous populations of DNA to be sorted to recover long targets for deep sequencing. It is valuable whenever a target sequence is rare in a mixed population, such as for characterizing mutations in heterogeneous cancer cell populations or identifying cells containing a specific genetic sequence or infected with a target virus.
引用
收藏
页数:9
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