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PathoScope 2.0: a complete computational framework for strain identification in environmental or clinical sequencing samples

机译:PathoScope 2.0:用于环境或临床测序样品中菌株鉴定的完整计算框架

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Background Recent innovations in sequencing technologies have provided researchers with the ability to rapidly characterize the microbial content of an environmental or clinical sample with unprecedented resolution. These approaches are producing a wealth of information that is providing novel insights into the microbial ecology of the environment and human health. However, these sequencing-based approaches produce large and complex datasets that require efficient and sensitive computational analysis workflows. Many recent tools for analyzing metagenomic-sequencing data have emerged, however, these approaches often suffer from issues of specificity, efficiency, and typically do not include a complete metagenomic analysis framework. Results We present PathoScope 2.0, a complete bioinformatics framework for rapidly and accurately quantifying the proportions of reads from individual microbial strains present in metagenomic sequencing data from environmental or clinical samples. The pipeline performs all necessary computational analysis steps; including reference genome library extraction and indexing, read quality control and alignment, strain identification, and summarization and annotation of results. We rigorously evaluated PathoScope 2.0 using simulated data and data from the 2011 outbreak of Shiga-toxigenic Escherichia coli O104:H4. Conclusions The results show that PathoScope 2.0 is a complete, highly sensitive, and efficient approach for metagenomic analysis that outperforms alternative approaches in scope, speed, and accuracy. The PathoScope 2.0 pipeline software is freely available for download at: http://sourceforge.net/projects/pathoscope/ webcite.
机译:背景技术测序技术的最新创新为研究人员提供了以前所未有的分辨率快速表征环境或临床样品中微生物含量的能力。这些方法产生了大量的信息,这些信息为环境和人类健康的微生物生态学提供了新颖的见解。但是,这些基于排序的方法会产生庞大而复杂的数据集,需要高效而敏感的计算分析工作流程。已经出现了许多用于分析宏基因组测序数据的最新工具,但是,这些方法经常遭受特异性,效率问题的困扰,并且通常不包括完整的宏基因组分析框架。结果我们提出了PathoScope 2.0,这是一个完整的生物信息学框架,可用于快速,准确地量化环境或临床样品的宏基因组测序数据中单个微生物菌株的读数比例。管道执行所有必要的计算分析步骤;包括参考基因组文库的提取和索引编制,读取质量控制和比对,菌株鉴定以及结果的汇总和注释。我们使用模拟数据和2011年志贺毒素大肠杆菌O104:H4爆发的数据严格评估了PathoScope 2.0。结论结果表明,PathoScope 2.0是一种完整,高度灵敏,高效的宏基因组分析方法,在范围,速度和准确性方面均优于其他方法。可从以下位置免费下载PathoScope 2.0管道软件:http://sourceforge.net/projects/pathoscope/webcite。

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