仆从
纳米孔测序
生物
DNA提取
DNA测序
计算生物学
DNA
纳米孔
遗传学
纳米技术
聚合酶链反应
材料科学
基因
作者
Inswasti Cahyani,John J. Tyson,Nadine Holmes,Joshua Quick,Christopher Moore,Nick Loman,Matthew Loose
出处
期刊:Genome Research
[Cold Spring Harbor Laboratory Press]
日期:2025-03-24
卷期号:35 (5): 1154-1166
被引量:1
标识
DOI:10.1101/gr.279943.124
摘要
Since the advent of long-read sequencing, achieving longer read lengths has been a key goal for many users. Ultra-long-read sets (N50 ≥ 100 kb) produced from Oxford Nanopore sequencers have improved genome assemblies in recent years. However, despite progress in extraction protocols and library preparation methods, ultra-long sequencing remains challenging for many sample types. Here, we compare various methods and introduce the FindingNemo protocol that: (1) optimizes ultra-high-molecular-weight (UHMW) DNA extraction and library cleanup by using glass beads and hexamminecobalt(III) chloride (CoHex), (2) can deliver high ultra-long sequencing yield of >20 Gb of reads from a single MinION flow cell or >100 Gb from PromethION devices (R9.4-R10.4 pore variants), and (3) is scalable to using fewer input cells or lower DNA amounts, with extraction to sequencing possible in a single working day. By comparison, we demonstrate that this protocol surpasses previous methods by enabling precise determination of input DNA quantity and quality through cell counting, sample dilution, and homogenization techniques.
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