在洪流中寻找条形码:从COI到NGS平台上的完整有丝分裂基因组

DNA Barcodes Pub Date : 1900-01-01 DOI:10.1515/DNA-2015-0019
D. Hinsinger, R. Debruyne, Maeva Thomas, G. Denys, M. Mennesson, Jose Utage, A. Dettai
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引用次数: 29

摘要

示例,适用于任何桌面NGS平台。它能够从流行的条形码方法扩展,从单一的COI转移到完整的有丝分裂基因组测序。摘要:采用经典COI条形码与基于sanger的测序方法相结合的新一代测序方法。在这里,我们描述了一个在NGS平台上对有丝分裂基因组进行测序和多路复用的框架,该框架实现了(I)基于通用远程pcr的扩增技术,(II)两级多路复用方法(即基于发散和特定标签索引),以及(III)来自Ion Torrent测序平台的专用多路复用和组装脚本。我们提供了一个有丝分裂基因组的案例研究,该案例研究获得了两个有丝分裂基因组的保证个体,并表明该工作流程可以在PGM测序仪上恢复每个测序芯片上超过100个有丝分裂基因组,将每个有丝分裂基因组的个体成本降至7,50欧元以下(截至目前的2015年测序成本)。在我们提出的改进dna条形码中,使用数千个碱基进行识别,强调了数据可靠性的需要,特别是通过元数据。基于科学和经济的考虑,该框架提出了一种相关的复用方法
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fishing for barcodes in the Torrent: from COI to complete mitogenomes on NGS platforms
samples, adaptable on any desktop NGS platform. It enables to extend from the prevalent barcoding approach by shifting from the single COI to complete mitogenome sequencing. Abstract: The adoption of Next-Generation Sequencing by the fit between the classical COI barcode and the Sanger-based sequencing method. Here we describe a framework for the sequencing and multiplexing of mitogenomes on NGS platforms that implements (I) a universal long-range PCR-based amplification technique, (II) a two-level multiplexing approach ( i.e. divergence-based and specific tag indexing), and (III) a dedicated demultiplexing and assembling script from an Ion Torrent sequencing platform. We provide a case study of mitogenomes obtained for two vouchered individuals of daces Leuciscus burdigalensis and L. oxyrrhis and show that this workflow enables to recover over 100 mitogenomes per sequencing chip on a PGM sequencer, bringing the individual cost down below 7,50€ per mitogenome (as of current 2015 sequencing costs). The use of several kilobases for identification purposes, as involved in the improved DNA-barcode we propose, stress the need for data reliability, especially through metadata. Based on both scientific and economic considerations, this framework presents a relevant approach for multiplexing
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