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Common Contaminants in Next-Generation Sequencing That Hinder Discovery of Low-Abundance Microbes

机译:下一代测序中的常见污染物阻碍了低丰度微生物的发现

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摘要

Unbiased high-throughput sequencing of whole metagenome shotgun DNA libraries is a promising new approach to identifying microbes in clinical specimens, which, unlike other techniques, is not limited to known sequences. Unlike most sequencing applications, it is highly sensitive to laboratory contaminants as these will appear to originate from the clinical specimens. To assess the extent and diversity of sequence contaminants, we aligned 57 “1000 Genomes Project” sequencing runs from six centers against the four largest NCBI BLAST databases, detecting reads of diverse contaminant species in all runs and identifying the most common of these contaminant genera (Bradyrhizobium) in assembled genomes from the NCBI Genome database. Many of these microorganisms have been reported as contaminants of ultrapure water systems. Studies aiming to identify novel microbes in clinical specimens will greatly benefit from not only preventive measures such as extensive UV irradiation of water and cross-validation using independent techniques, but also a concerted effort to sequence the complete genomes of common contaminants so that they may be subtracted computationally.
机译:完整的基因组shot弹枪DNA文库的无偏高通量测序是鉴定临床标本中微生物的一种有前途的新方法,与其他技术不同,该方法不限于已知序列。与大多数测序应用不同,它对实验室污染物高度敏感,因为这些污染物似乎源自临床标本。为了评估序列污染物的程度和多样性,我们将来自六个中心的57个“ 1000个基因组计划”测序运行与四个最大的NCBI BLAST数据库进行比对,检测所有运行中各种污染物种类的读数,并确定这些污染物属中最常见的(来自NCBI Genome数据库的已组装基因组中的Bradyrhizobium)。据报道,其中许多微生物是超纯水系统的污染物。旨在识别临床标本中新微生物的研究不仅会受益于预防措施,例如广泛的紫外线照射和使用独立技术的交叉验证,而且还将共同努力对常见污染物的完整基因组进行测序,以便计算上减去。

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