A Quantitative Comparison of Single-Cell Whole Genome Amplification Methods

被引:217
|
作者
de Bourcy, Charles F. A. [1 ]
De Vlaminck, Iwijn [1 ,2 ,4 ]
Kanbar, Jad N. [2 ,4 ]
Wang, Jianbin [2 ]
Gawad, Charles [1 ,2 ,3 ]
Quake, Stephen R. [1 ,2 ,4 ]
机构
[1] Stanford Univ, Dept Appl Phys, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Dept Pediat, Div Hematol Oncol Stem Cell Transplantat & Canc B, Stanford, CA 94305 USA
[4] Stanford Univ, Howard Hughes Med Inst, Stanford, CA 94305 USA
来源
PLOS ONE | 2014年 / 9卷 / 08期
基金
美国能源部; 美国国家科学基金会;
关键词
MULTIPLE DISPLACEMENT AMPLIFICATION; EVOLUTION; ALIGNMENT; CLONING; RARE;
D O I
10.1371/journal.pone.0105585
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
Single-cell sequencing is emerging as an important tool for studies of genomic heterogeneity. Whole genome amplification (WGA) is a key step in single-cell sequencing workflows and a multitude of methods have been introduced. Here, we compare three state-of-the-art methods on both bulk and single-cell samples of E. coli DNA: Multiple Displacement Amplification (MDA), Multiple Annealing and Looping Based Amplification Cycles (MALBAC), and the PicoPLEX single-cell WGA kit (NEB-WGA). We considered the effects of reaction gain on coverage uniformity, error rates and the level of background contamination. We compared the suitability of the different WGA methods for the detection of copy-number variations, for the detection of single-nucleotide polymorphisms and for de-novo genome assembly. No single method performed best across all criteria and significant differences in characteristics were observed; the choice of which amplifier to use will depend strongly on the details of the type of question being asked in any given experiment.
引用
收藏
页数:9
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