首页> 外文期刊>Frontiers in Marine Science >MinION-in-ARMS: Nanopore Sequencing to Expedite Barcoding of Specimen-Rich Macrofaunal Samples From Autonomous Reef Monitoring Structures
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MinION-in-ARMS: Nanopore Sequencing to Expedite Barcoding of Specimen-Rich Macrofaunal Samples From Autonomous Reef Monitoring Structures

机译:碎裂的武器:纳米孔测序,加快自主珊瑚礁监测结构的富含样品富含富含型宏观样品的条形码

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Autonomous Reef Monitoring Structure (ARMS) are standardised devices for sampling biodiversity in complex marine benthic habitats such as coral reefs. When coupled with DNA sequencing, these devices greatly expand our ability to document marine biodiversity. Unfortunately, the existing workflow for processing macrofaunal samples (2-mm) in the ARMS pipeline—which involves Sanger sequencing—is expensive, laborious, and thus prohibitive for ARMS researchers. Here, we propose a faster, more cost-effective alternative by demonstrating a successful application of the MinION-based barcoding approach on the 2mm-size fraction of ARMS samples. All data were available within 3.5–4 h, and sequencing costs relatively low at approximately US$3 per MinION barcode. We sequenced the 313-bp fragment of the cytochrome c oxidase subunit I (COI) for 725 samples on both MinION and Illumina platforms, and retrieved 507–584 overlapping barcodes. MinION barcodes were highly accurate (~99.9%) when compared with Illumina reference barcodes. Molecular operational taxonomic units inferred between MinION and Illumina barcodes were consistently stable, and match ratios demonstrated highly congruent clustering patterns (≥0.96). Our method would make ARMS more accessible to researchers, and greatly expedite the processing of macrofaunal samples; it can also be easily applied to other small-to-moderate DNA barcoding projects (10,000 specimens) for rapid species identification and discovery.
机译:自主礁监测结构(武器)是用于在复杂的海洋底栖栖息地(如珊瑚礁)中的生物多样性的标准化装置。当与DNA测序结合时,这些器件大大扩大了我们记录海洋生物多样性的能力。遗憾的是,用于在武器管道中加工宏指令样品(> 2毫米)的现有工作流程 - 这涉及桑格测序 - 昂贵,艰巨,从而对武器研究人员来说令人望而却步。在这里,我们通过证明在> 2mm尺寸的武器样品分数上成功地应用了一种更快,更具成本效益的替代方案。所有数据都在3.5-4小时内获得,并且每块条形码约为3美元,测序成本相对较低。我们对矿物和Illumina平台进行了725个样品的细胞色素C氧化酶亚基I(COI)的313-BP片段,并检索了507-584重叠条形码。与Illumina参考条形码相比,甲基条子区高精度(〜99.9%)。分子运行分类单位推断在甲基和illumina条形码之间始终稳定,并且匹配比率表现出高度全体聚类模式(≥0.96)。我们的方法将使武器更加访问研究人员,并大大加快加工宏观式样本;它也可以很容易地应用于其他小于适度的DNA条形码项目(<10,000个标本),用于快速物种鉴定和发现。

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