仆从
基因组
纳米孔测序
生物
基因组
计算生物学
Illumina染料测序
多路复用
硅胶PCR
DNA测序
深度测序
寨卡病毒
全基因组测序
遗传学
多重聚合酶链反应
病毒
聚合酶链反应
基因
作者
Josh Quick,Nathan D. Grubaugh,Steven T. Pullan,Ingra Morales Claro,Andrew D. Smith,Karthik Gangavarapu,Glenn Oliveira,Refugio Robles‐Sikisaka,Thomas F. Rogers,Nathan Beutler,Dennis R. Burton,Lia Laura Lewis‐Ximenez,Jaqueline Góes de Jesus,Marta Giovanetti,Sarah C. Hill,Allison Black,Trevor Bedford,Miles W. Carroll,Márcio Roberto Teixeira Nunes,Luíz Carlos Júnior Alcântara
出处
期刊:
[Cold Spring Harbor Laboratory]
日期:2017-01-09
被引量:60
摘要
Genome sequencing has become a powerful tool for studying emerging infectious diseases; however, genome sequencing directly from clinical samples without isolation remains challenging for viruses such as Zika, where metagenomic sequencing methods may generate insufficient numbers of viral reads. Here we present a protocol for generating coding-sequence complete genomes comprising an online primer design tool, a novel multiplex PCR enrichment protocol, optimised library preparation methods for the portable MinION sequencer (Oxford Nanopore Technologies) and the Illumina range of instruments, and a bioinformatics pipeline for generating consensus sequences. The MinION protocol does not require an internet connection for analysis, making it suitable for field applications with limited connectivity. Our method relies on multiplex PCR for targeted enrichment of viral genomes from samples containing as few as 50 genome copies per reaction. Viral consensus sequences can be achieved starting with clinical samples in 1-2 days following a simple laboratory workflow. This method has been successfully used by several groups studying Zika virus evolution and is facilitating an understanding of the spread of the virus in the Americas.
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