Inexpensive Multiplexed Library Preparation for Megabase-Sized Genomes

被引:466
作者
Baym, Michael [1 ]
Kryazhimskiy, Sergey [2 ,3 ]
Lieberman, Tami D. [1 ]
Chung, Hattie [1 ]
Desai, Michael M. [2 ,3 ,4 ]
Kishony, Roy [1 ,5 ,6 ]
机构
[1] Harvard Univ, Sch Med, Dept Syst Biol, Boston, MA USA
[2] Harvard Univ, Dept Organism & Evolutionary Biol, Cambridge, MA 02138 USA
[3] Harvard Univ, FAS Ctr Syst Biol, Cambridge, MA 02138 USA
[4] Harvard Univ, Dept Phys, Cambridge, MA 02138 USA
[5] Technion Israel Inst Technol, Fac Biol, Haifa, Israel
[6] Technion Israel Inst Technol, Dept Comp Sci, IL-32000 Haifa, Israel
基金
欧洲研究理事会; 美国国家科学基金会; 美国国家卫生研究院;
关键词
EXPERIMENTAL EVOLUTION; LOW-INPUT; PCR;
D O I
10.1371/journal.pone.0128036
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
Whole-genome sequencing has become an indispensible tool of modern biology. However, the cost of sample preparation relative to the cost of sequencing remains high, especially for small genomes where the former is dominant. Here we present a protocol for rapid and inexpensive preparation of hundreds of multiplexed genomic libraries for Illumina sequencing. By carrying out the Nextera tagmentation reaction in small volumes, replacing costly reagents with cheaper equivalents, and omitting unnecessary steps, we achieve a cost of library preparation of $ 8 per sample, approximately 6 times cheaper than the standard Nextera XT protocol. Furthermore, our procedure takes less than 5 hours for 96 samples. Several hundred samples can then be pooled on the same HiSeq lane via custom barcodes. Our method will be useful for re-sequencing of microbial or viral genomes, including those from evolution experiments, genetic screens, and environmental samples, as well as for other sequencing applications including large amplicon, open chromosome, artificial chromosomes, and RNA sequencing.
引用
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页数:15
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