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使用 MinION 和 Illumina 测序进行基因组学研究可实现基因组的完成和纠错。

Genomics Using MinION and Illumina Sequencing Enables Genome Completion and Correction.

机构信息

Department of Biomedical Sciences and Pathology, Virginia-Maryland College of Veterinary Medicine, Blacksburg, Virginia, USA.

Advanced Research Computing, Virginia Polytechnic Institute and State University, Blacksburg, Virginia, USA.

出版信息

mSphere. 2018 Jul 5;3(4):e00269-18. doi: 10.1128/mSphere.00269-18.

Abstract

Understanding the virulence mechanisms of human pathogens from the genus has been hindered by a lack of properly assembled and annotated genomes. Here we report the first complete genomes for seven strains, as well as resequencing of the reference strain subsp. ATCC 25586 (total of seven species; total of eight genomes). A highly efficient and cost-effective sequencing pipeline was achieved using sample multiplexing for short-read Illumina (150 bp) and long-read Oxford Nanopore MinION (>80 kbp) platforms, coupled with genome assembly using the open-source software Unicycler. Compared to currently available draft assemblies (previously 24 to 67 contigs), these genomes are highly accurate and consist of only one complete chromosome. We present the complete genome sequence of subsp. ATCC 23726, a genetically tractable and biomedically important strain and, in addition, reveal that the previous subsp. ATCC 25586 genome assembly contains a 452-kb genomic inversion that has been corrected using our sequencing and assembly pipeline. To enable genomic analyses by the scientific community, we concurrently used these genomes to launch FusoPortal, a repository of interactive and downloadable genomic data, genome maps, gene annotations, and protein functional analyses and classifications. In summary, this report provides detailed methods for accurately sequencing, assembling, and annotating genomes, while focusing on using open-source software to foster the availability of reproducible and open data. This resource will enhance efforts to properly identify virulence proteins that may contribute to a repertoire of diseases that includes periodontitis, preterm birth, and colorectal cancer. spp. are Gram-negative, oral bacteria that are increasingly associated with human pathologies as diverse as periodontitis, preterm birth, and colorectal cancer. While a recent surge in research has increased our understanding of this human pathogen, a lack of complete genomes has hindered the identification and characterization of associated host-pathogen virulence factors. Here we report the first eight complete genomes sequenced using an Oxford Nanopore MinION and Illumina sequencing pipeline and assembled using the open-source program Unicycler. These genomes are highly accurate, and seven of the genomes represent the first complete sequences for each strain. In summary, the FusoPortal resource provides a publicly available resource that will guide future genetic, bioinformatic, and biochemical experiments to characterize this genus of emerging human pathogens.

摘要

从 属种理解人类病原体的毒力机制一直受到缺乏适当组装和注释基因组的阻碍。在这里,我们报告了七个 菌株的第一个完整基因组,以及参考菌株 subsp. ATCC 25586 的重测序(共七种物种;共八种基因组)。通过使用短读长 Illumina(150bp)和长读长 Oxford Nanopore MinION(>80kbp)平台的样本多路复用,结合使用开源软件 Unicycler 进行基因组组装,实现了一种高效且具有成本效益的测序管道。与当前可用的草图组装相比(以前是 24 到 67 个 contigs),这些基因组高度准确,仅由一个完整的染色体组成。我们介绍了 subsp. ATCC 23726 的完整基因组序列,这是一种遗传上可操作和具有重要生物医学意义的菌株,此外,我们还揭示了以前的 subsp. ATCC 25586 基因组组装包含一个 452kb 的基因组倒位,我们使用测序和组装管道对其进行了纠正。为了使科学界能够进行基因组分析,我们同时使用这些基因组启动了 FusoPortal,这是一个交互式和可下载基因组数据、基因组图谱、基因注释和蛋白质功能分析和分类的存储库。总之,本报告提供了详细的方法来准确测序、组装和注释 基因组,同时专注于使用开源软件来促进可重复和开放数据的可用性。该资源将增强正确识别可能导致牙周炎、早产和结直肠癌等多种疾病的毒力蛋白的努力。 spp. 是革兰氏阴性的口腔细菌,与牙周炎、早产和结直肠癌等多种人类病理越来越相关。尽管最近对 的研究激增增加了我们对这种人类病原体的理解,但缺乏完整的基因组阻碍了相关宿主-病原体毒力因子的鉴定和表征。在这里,我们报告了使用 Oxford Nanopore MinION 和 Illumina 测序管道测序并使用开源程序 Unicycler 组装的前八个完整 基因组。这些基因组高度准确,其中七个基因组代表每个菌株的第一个完整序列。总之,FusoPortal 资源提供了一个公开可用的资源,将指导未来的遗传、生物信息学和生物化学实验,以表征这个新兴的人类病原体属。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a880/6034080/bf389126fdd2/sph0041825850001.jpg

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