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MinION 16S datasets of a commercially available microbial community enables the evaluation of DNA extractions and data analyses

机译:Minion 16S商业微生物群落的数据集能够评估DNA提取和数据分析

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摘要

New advances in sequencing technology and bioinformatics analysis tools have significantly supported the culture-independent analysis of complex microbial communities associated with environmental, plant, animal and human samples. However, previous work has shown that DNA extraction can have a major influence in the community profile. As such there is a constant need for new methods to efficiently and rapidly prepare and analyze DNA for microbiome research, especially in the case new and emerging technology like the Oxford Nanopore Technologies (ONT) MinION. A commercial standard was used, in triplicate, to evaluate three DNA extraction protocols, including two commercially available and one ”in-house” DNA extraction method. All DNA extractions were done as per manufacturer's instructions and prepared with the same commercial ONT 16S sample preparation kit, prior to being analysed using MinION sequencing. Eight MinION 16S datasets of this microbial reference community were obtained. Reads were initially base called and demultiplexed using ONT's Guppy™ sequencing software (version 3.2.4), filtered using NanoFilt and then classified using Usearch. A set of R scripts are presented to process sintax files generated from Usearch and produce an OTU table that can be used for further analyses. All datasets were deposited into the SRA (NCBI) database. These datasets will allow future extraction kit comparisons using MinION sequencing since a standardize laboratory process using commercially available components, such as the MinION 16S sample preparation kit, microbial reference community and extraction kits, were used. The current ONT 16S workflow making use of the Epi2me agent only provides QC metrics and the ID's of the main genera identified and does not provide any tools currently for further downstream community comparison. The analyses scripts provided in the supplementary material will thus further enable the testing of new datasets against these reference sets and provide users the ability to compare their workflows with ours, thus standardizing comparisons and workflows.
机译:测序技术和生物信息学分析工具的新进展显着支持与环境,植物,动物和人类样品相关的复杂微生物社区的文化自主分析。然而,之前的工作表明,DNA提取可能对社区概况产生重大影响。因此,持续需要有效且迅速准备和分析DNA进行微生物组研究的新方法,特别是在牛津纳米孔技术(ONT)矿物等新的和新兴技术。将商业标准一式三份使用,以评估三种DNA提取方案,包括两种可商购和一个“内部”DNA提取方法。所有DNA提取物按照厂家的指示进行,并在使用碎片测序分析之前用相同的商业ONT 16S样品制备试剂盒制备。获得了八分钟的16S这种微生物参考社区的数据集。读取最初是由ONT的Guppy™测序软件(版本3.2.4)调用和解复用的基础,使用nanofilt过滤,然后使用usearch进行分类。展示了一组R脚本以处理从USearch生成的Sintax文件,并生成可用于进一步分析的OTU表。所有数据集都存放到SRA(NCBI)数据库中。由于使用商业上可用组分的标准化实验室方法,这些数据集将使用甲酸序测序的未来提取套件比较,例如使用商业上可用的组分,例如MOION 16S样品制备试剂盒,微生物参考群落和提取试剂盒。目前的ONT 16S工作流利用EPI2ME代理仅提供QC度量标准,并且所识别的主机的ID,并且不提供目前进一步下游社区比较的任何工具。因此,在补充材料中提供的分析脚本将进一步实现对这些参考集的新数据集的测试,并为用户提供与我们的工作流程进行比较的能力,从而标准化比较和工作流程。

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