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nanoMLST: accurate multilocus sequence typing using Oxford Nanopore Technologies MinION with a dual-barcode approach to multiplex large numbers of samples

机译:Nanomlst:准确使用牛津纳米孔技术沟通的多层序列,用双条码方法进行多元条码方法来复用大量样品

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Multilocus sequence typing (MLST) is one of the most commonly used methods for studying microbial lineage worldwide. However, the traditional MLST process using Sanger sequencing is time-consuming and expensive. We have designed a workflow that simultaneously sequenced seven full-length housekeeping genes of 96 meticillin-resistant Staphylococcus aureus isolates with dual-barcode multiplexing using just a single flow cell of an Oxford Nanopore Technologies MinION system, and then we performed bioinformatic analysis for strain typing. Fifty-one of the isolates comprising 34 sequence types had been characterized using Sanger sequencing. We demonstrate that the allele assignments obtained by our nanopore workflow (nanoMLST, available at https://github.com/jade-nhri/nanoMLST) were identical to those obtained by Sanger sequencing (359/359, with 100 % agreement rate). In addition, we estimate that our multiplex system is able to perform MLST for up to 1000 samples simultaneously; thus, providing a rapid and cost-effective solution for molecular typing.
机译:多焦序列键入(MLST)是在全球研究微生物谱系的最常用方法之一。然而,使用Sanger测序的传统MLST过程是耗时和昂贵的。我们设计了一种工作流程,其同时使用牛津纳米孔技术成型系统的单个流量电池进行了与双条码多路复用的96个型耐含有96个抗性金黄色葡萄球菌的全长家用基因,然后进行生物信息分析进行应变键入。使用Sanger测序表征了包含34种序列类型的50-一体的分离物。我们证明我们的纳米孔工作流程(Nanomlst,Https://github.com/jade-nhri/nanomlst获得的等位基因分配与Sanger测序(359/359,达100%协议率)获得的等位基因分配相同。此外,我们估计我们的多路复用系统能够同时执行高达1000个样本的MLST;因此,为分子打字提供了一种快速且经济效益的解决方案。

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