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使用电子探针诊断核酸检测法筛选宏基因组数据中的病毒。

Screening metagenomic data for viruses using the e-probe diagnostic nucleic acid assay.

作者信息

Stobbe A H, Schneider W L, Hoyt P R, Melcher U

出版信息

Phytopathology. 2014 Oct;104(10):1125-9. doi: 10.1094/PHYTO-11-13-0310-R.

Abstract

Next generation sequencing (NGS) is not used commonly in diagnostics, in part due to the large amount of time and computational power needed to identify the taxonomic origin of each sequence in a NGS data set. By using the unassembled NGS data sets as the target for searches, pathogen-specific sequences, termed e-probes, could be used as queries to enable detection of specific viruses or organisms in plant sample metagenomes. This method, designated e-probe diagnostic nucleic acid assay, first tested with mock sequence databases, was tested with NGS data sets generated from plants infected with a DNA (Bean golden yellow mosaic virus, BGYMV) or an RNA (Plum pox virus, PPV) virus. In addition, the ability to detect and differentiate among strains of a single virus species, PPV, was examined by using probe sets that were specific to strains. The use of probe sets for multiple viruses determined that one sample was dually infected with BGYMV and Bean golden mosaic virus.

摘要

下一代测序(NGS)在诊断中并不常用,部分原因是要确定NGS数据集中每个序列的分类学来源需要大量时间和计算能力。通过将未组装的NGS数据集作为搜索目标,病原体特异性序列(称为电子探针)可作为查询工具,用于检测植物样本宏基因组中的特定病毒或生物体。这种方法称为电子探针诊断核酸检测法,首先在模拟序列数据库中进行测试,然后用感染了DNA病毒(菜豆金黄花叶病毒,BGYMV)或RNA病毒(李痘病毒,PPV)的植物所产生的NGS数据集进行测试。此外,通过使用针对毒株的探针组,研究了检测单一病毒物种PPV的毒株并进行区分的能力。针对多种病毒使用探针组确定了一个样本同时感染了BGYMV和菜豆金黄花叶病毒。

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