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Validation of a Bioinformatics Workflow for Routine Analysis of Whole-Genome Sequencing Data and Related Challenges for Pathogen Typing in a European National Reference Center: Neisseria meningitidis as a Proof-of-Concept

机译:在欧洲国家参考中心对全基因组测序数据进行例行分析的生物信息学工作流程的验证以及病原体分型的相关挑战:脑膜炎奈瑟氏菌作为概念验证

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摘要

Despite being a well-established research method, the use of whole-genome sequencing (WGS) for routine molecular typing and pathogen characterization remains a substantial challenge due to the required bioinformatics resources and/or expertise. Moreover, many national reference laboratories and centers, as well as other laboratories working under a quality system, require extensive validation to demonstrate that employed methods are “fit-for-purpose” and provide high-quality results. A harmonized framework with guidelines for the validation of WGS workflows does currently, however, not exist yet, despite several recent case studies highlighting the urgent need thereof. We present a validation strategy focusing specifically on the exhaustive characterization of the bioinformatics analysis of a WGS workflow designed to replace conventionally employed molecular typing methods for microbial isolates in a representative small-scale laboratory, using the pathogen Neisseria meningitidis as a proof-of-concept. We adapted several classically employed performance metrics specifically toward three different bioinformatics assays: resistance gene characterization (based on the ARG-ANNOT, ResFinder, CARD, and NDARO databases), several commonly employed typing schemas (including, among others, core genome multilocus sequence typing), and serogroup determination. We analyzed a core validation dataset of 67 well-characterized samples typed by means of classical genotypic and/or phenotypic methods that were sequenced in-house, allowing to evaluate repeatability, reproducibility, accuracy, precision, sensitivity, and specificity of the different bioinformatics assays. We also analyzed an extended validation dataset composed of publicly available WGS data for 64 samples by comparing results of the different bioinformatics assays against results obtained from commonly used bioinformatics tools. We demonstrate high performance, with values for all performance metrics >87%, >97%, and >90% for the resistance gene characterization, sequence typing, and serogroup determination assays, respectively, for both validation datasets. Our WGS workflow has been made publicly available as a “push-button” pipeline for Illumina data at to showcase its implementation for non-profit and/or academic usage. Our validation strategy can be adapted to other WGS workflows for other pathogens of interest and demonstrates the added value and feasibility of employing WGS with the aim of being integrated into routine use in an applied public health setting.
机译:尽管是成熟的研究方法,但是由于所需的生物信息学资源和/或专业知识,使用全基因组测序(WGS)进行常规分子分型和病原体表征仍然是一项重大挑战。此外,许多国家参考实验室和中心,以及在质量体系下工作的其他实验室,都需要进行广泛的验证,以证明所采用的方法“适合目的”并提供高质量的结果。尽管最近有一些案例研究强调了这一迫切需求,但目前尚不存在一个用于验证WGS工作流的准则的统一框架。我们提出一种验证策略,专门针对WGS工作流程的生物信息学分析进行详尽的表征,该工作流程旨在代替代表性的小型实验室中的微生物分离株使用微生物分离株的常规采用的分子分型方法,以病原体脑膜炎奈瑟氏菌为概念验证。我们针对三种不同的生物信息学检测方法调整了几种经典采用的性能指标:抗性基因表征(基于ARG-ANNOT,ResFinder,CARD和NDARO数据库),几种常用的输入模式(包括核心基因组多基因座序列类型) )和血清群测定。我们分析了67种特征明确的样本的核心验证数据集,这些样本通过内部测序的经典基因型和/或表型方法进行了分类,从而可以评估不同生物信息学测定法的重复性,再现性,准确性,精密度,敏感性和特异性。我们还通过比较不同生物信息学测定的结果与从常用生物信息学工具获得的结果,分析了由64个样品的公共WGS数据组成的扩展验证数据集。我们证明了高性能,两个验证数据集的所有性能指标值均分别大于87%,> 97%和> 90%,分别用于抗性基因表征,序列分型和血清群测定分析。我们的WGS工作流程已作为Illumina数据的“按钮”管道公开发布,以展示其在非营利和/或学术用途上的实施。我们的验证策略可适用于其他WGS工作流以处理其他感兴趣的病原体,并证明了采用WGS的附加价值和可行性,目的是将WGS整合到应用公共卫生环境中的常规使用中。

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