Deschamps Stéphane, Mudge Joann, Cameron Connor, Ramaraj Thiruvarangan, Anand Ajith, Fengler Kevin, Hayes Kevin, Llaca Victor, Jones Todd J, May Gregory
DuPont Pioneer, Johnston, IA, USA.
National Center for Genome Resources, Santa Fe, NM, USA.
Sci Rep. 2016 Jun 28;6:28625. doi: 10.1038/srep28625.
The MinION is a portable single-molecule DNA sequencing instrument that was released by Oxford Nanopore Technologies in 2014, producing long sequencing reads by measuring changes in ionic flow when single-stranded DNA molecules translocate through the pores. While MinION long reads have an error rate substantially higher than the ones produced by short-read sequencing technologies, they can generate de novo assemblies of microbial genomes, after an initial correction step that includes alignment of Illumina sequencing data or detection of overlaps between Oxford Nanopore reads to improve accuracy. In this study, MinION reads were generated from the multi-chromosome genome of Agrobacterium tumefaciens strain LBA4404. Errors in the consensus two-directional (sense and antisense) "2D" sequences were first characterized by way of comparison with an internal reference assembly. Both Illumina-based correction and self-correction were performed and the resulting corrected reads assembled into high-quality hybrid and non-hybrid assemblies. Corrected read datasets and assemblies were subsequently compared. The results shown here indicate that both hybrid and non-hybrid methods can be used to assemble Oxford Nanopore reads into informative multi-chromosome assemblies, each with slightly different outcomes in terms of contiguity and accuracy.
MinION是牛津纳米孔技术公司于2014年推出的一款便携式单分子DNA测序仪,它通过测量单链DNA分子穿过孔隙时离子流的变化来生成长测序读段。虽然MinION长读段的错误率远高于短读测序技术产生的读段,但在经过包括比对Illumina测序数据或检测牛津纳米孔读段之间的重叠以提高准确性的初始校正步骤后,它们能够生成微生物基因组的从头组装。在本研究中,从根癌农杆菌菌株LBA4404的多染色体基因组生成了MinION读段。首先通过与内部参考组装进行比较来表征一致双向(正向和反向)“2D”序列中的错误。进行了基于Illumina的校正和自我校正,并将得到的校正读段组装成高质量的混合和非混合组装。随后比较了校正读段数据集和组装。此处显示的结果表明,混合和非混合方法均可用于将牛津纳米孔读段组装成信息丰富的多染色体组装,每种方法在连续性和准确性方面的结果略有不同。