DNA测序
微流控
计算生物学
基因组
计算机科学
基因组DNA
可扩展性
DNA
生物
纳米技术
遗传学
数据库
基因
材料科学
作者
Hanyoup Kim,Mais J. Jebrail,Anupama Sinha,Zachary Bent,Owen D. Solberg,Kelly P. Williams,Stanley A. Langevin,Ronald F. Renzi,James L. Van De Vreugde,Robert J. Meagher,Joseph S. Schoeniger,Todd W. Lane,Steven S. Branda,Michael Bartsch,Kamlesh D. Patel
出处
期刊:PLOS ONE
[Public Library of Science]
日期:2013-07-22
卷期号:8 (7): e68988-e68988
被引量:101
标识
DOI:10.1371/journal.pone.0068988
摘要
Next-generation sequencing (NGS) is emerging as a powerful tool for elucidating genetic information for a wide range of applications. Unfortunately, the surging popularity of NGS has not yet been accompanied by an improvement in automated techniques for preparing formatted sequencing libraries. To address this challenge, we have developed a prototype microfluidic system for preparing sequencer-ready DNA libraries for analysis by Illumina sequencing. Our system combines droplet-based digital microfluidic (DMF) sample handling with peripheral modules to create a fully-integrated, sample-in library-out platform. In this report, we use our automated system to prepare NGS libraries from samples of human and bacterial genomic DNA. E. coli libraries prepared on-device from 5 ng of total DNA yielded excellent sequence coverage over the entire bacterial genome, with >99% alignment to the reference genome, even genome coverage, and good quality scores. Furthermore, we produced a de novo assembly on a previously unsequenced multi-drug resistant Klebsiella pneumoniae strain BAA-2146 (KpnNDM). The new method described here is fast, robust, scalable, and automated. Our device for library preparation will assist in the integration of NGS technology into a wide variety of laboratories, including small research laboratories and clinical laboratories.
科研通智能强力驱动
Strongly Powered by AbleSci AI