纳米孔测序
DNA测序
杂交基因组组装
结扎测序
计算生物学
仆从
基因组
转座酶
DNA
基因组学
霰弹枪测序
顺序装配
基因组文库
DNA纳米球测序
生物
DNA测序器
杂交测序
单分子实时测序
纳米孔
遗传学
转座因子
基因
纳米技术
转录组
基序列
材料科学
基因表达
作者
Liang Gong,Chee-Hong Wong,Jennifer Idol,Chew Yee Ngan,Chia‐Lin Wei
摘要
Third generation single-molecule DNA sequencing technologies offer significantly longer read length that can facilitate the assembly of complex genomes and analysis of complex structural variants. Nanopore platforms perform single-molecule sequencing by directly measuring the current changes mediated by DNA passage through the pores and can generate hundreds of kilobase (kb) reads with minimal capital cost. This platform has been adopted by many researchers for a variety of applications. Achieving longer sequencing read lengths is the most critical factor to leverage the value of nanopore sequencing platforms. To generate ultra-long reads, special consideration is required to avoid DNA breakages and gain efficiency to generate productive sequencing templates. Here, we provide the detailed protocol of ultra-long DNA sequencing including high molecular weight (HMW) DNA extraction from fresh or frozen cells, library construction by mechanical shearing or transposase fragmentation, and sequencing on a nanopore device. From 20-25 µg of HMW DNA, the method can achieve N50 read length of 50-70 kb with mechanical shearing and N50 of 90-100 kb read length with transposase mediated fragmentation. The protocol can be applied to DNA extracted from mammalian cells to perform whole genome sequencing for the detection of structural variants and genome assembly. Additional improvements on the DNA extraction and enzymatic reactions will further increase the read length and expand its utility.
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