首页> 外文期刊>Journal of Clinical Microbiology >A Bioinformatics Whole-Genome Sequencing Workflow for Clinical Mycobacterium tuberculosis Complex Isolate Analysis, Validated Using a Reference Collection Extensively Characterized with Conventional Methods and In Silico Approaches
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A Bioinformatics Whole-Genome Sequencing Workflow for Clinical Mycobacterium tuberculosis Complex Isolate Analysis, Validated Using a Reference Collection Extensively Characterized with Conventional Methods and In Silico Approaches

机译:生物信息学全基因组测序工作流程用于临床<命名含量含量型=“属型”>分枝杆菌结核病复杂的分离分析,使用具有传统方法和<斜体切换= <斜体切换=的参考集合验证。 “是”>在Silico 方法中

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ABSTRACT The use of whole-genome sequencing (WGS) for routine typing of bacterial isolates has increased substantially in recent years. For Mycobacterium tuberculosis (MTB), in particular, WGS has the benefit of drastically reducing the time required to generate results compared to most conventional phenotypic methods. Consequently, a multitude of solutions for analyzing WGS MTB data have been developed, but their successful integration in clinical and national reference laboratories is hindered by the requirement for their validation, for which a consensus framework is still largely absent. We developed a bioinformatics workflow for (Illumina) WGS-based routine typing of MTB complex (MTBC) member isolates allowing complete characterization, including (sub)species confirmation and identification (16S, csb /RD, hsp65 ), single nucleotide polymorphism (SNP)-based antimicrobial resistance (AMR) prediction, and pathogen typing (spoligotyping, SNP barcoding, and core genome multilocus sequence typing). Workflow performance was validated on a per-assay basis using a collection of 238 in-house-sequenced MTBC isolates, extensively characterized with conventional molecular biology-based approaches supplemented with public data. For SNP-based AMR prediction, results from molecular genotyping methods were supplemented with in silico modified data sets, allowing us to greatly increase the set of evaluated mutations. The workflow demonstrated very high performance with performance metrics of &99% for all assays, except for spoligotyping, where sensitivity dropped to ~90%. The validation framework for our WGS-based bioinformatics workflow can aid in the standardization of bioinformatics tools by the MTB community and other SNP-based applications regardless of the targeted pathogen(s). The bioinformatics workflow is available for academic and nonprofit use through the Galaxy instance of our institute at https://galaxy.sciensano.be .
机译:摘要近年来,对常规键入细菌分离株的常规键入的全基因组测序(WGS)的使用增加。对于结核分枝杆菌(MTB),特别是WGS具有大大减少与大多数常规表型方法相比产生结果所需的时间的益处。因此,已经开发了用于分析WGS MTB数据的多种解决方案,但他们在临床和国家参考实验室中的成功整合因其验证的要求而受到阻碍,其中一项共识框架仍然很大程度上。我们开发了一种(Illumina)的基于MTB复合物(MTBC)成员分离物的生物信息学工作流程,允许完全表征,包括(子)物种确认和鉴定(16s,CSB / Rd,Hsp65),单核苷酸多态性(SNP)基于抗微生物抗性(AMR)预测和病原体键入(Spoligotyping,SNP条形码和核心基因组多层序列键入)。使用238个内部测序的MTBC隔离物的集合验证了工作流程,以238个内部测序的MTBC分离液进行广泛的特征,以常规的基于分子生物学的方法补充有公共数据。对于基于SNP的AMR预测,在硅改性数据集中补充了分子基因分型方法的结果,使我们能够大大增加评估突变。工作流程表现出非常高的性能,性能度量为&amp; 所有测定的99%,除了尖锐型分析,敏感性降至〜90%。基于WGS的生物信息学工作流程的验证框架可以帮助MTB社区和其他基于SNP的应用程序的生物信息学工具的标准化,而不管有针对性的病原体。生物信息学工作流程可通过在Https://galaxy.sciensano.be的学院的Galaxy实例中使用学术和非营利组织。

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