Illumina染料测序
基因组
DNA测序
计算生物学
深度测序
工作流程
霰弹枪测序
大规模并行测序
杂交基因组组装
生物
计算机科学
基因组
遗传学
DNA
基因
数据库
作者
Alessandra Modi,Stefania Vai,David Caramelli,Martina Lari
标识
DOI:10.1007/978-1-0716-1099-2_2
摘要
The NovaSeq 6000 is a sequencing platform from Illumina that enables the sequencing of short reads with an output up to 6 Tb. The NovaSeq 6000 uses the typical Illumina sequencing workflow based on library preparation, cluster generation by in situ amplification, and sequencing by synthesis. Flexibility is one of the major features of the NovaSeq 6000. Several types of sequencing kits coupled with dual flow cell mode enable high scalability of sequencing outputs to match a wide range of applications from complete genome sequencing to metagenomics analysis. In this chapter, after explaining how to assemble a normalized pool of libraries for sequencing, we will describe the experimental steps required to run the pools on the NovaSeq 6000 platform.
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