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引用次数: 0
摘要
外源 DNA 污染是单一生物古 DNA(aDNA)研究中的一个重大挑战。如果不能解决微生物、试剂和现今来源的污染问题,就会影响结果的解读。虽然已有野外和实验室规程来限制污染,但仍需要通过计算来准确区分内源和外源数据。在此,我们提出了一种基于元基因组分类器减少外源污染的工作流程。以往的方法完全依赖DNA测序读数与单一参考基因组的特异性映射来去除污染读数,而我们的方法则不同,在映射到参考基因组之前使用基于Kraken2的过滤。我们使用模拟和经验霰弹枪 aDNA 数据表明,这种工作流程是一种简单高效的方法,可用于各种计算环境,包括个人计算机。我们提出了建立用于测序数据分析的特定数据库的策略,其中考虑到了可用的计算资源以及关于目标类群和可能污染物的先验知识。我们的工作流程大大减少了测绘过程中所需的总体计算资源,并将总运行时间减少了约 94%。在低内源性样本中观察到的影响最为明显。重要的是,使用我们的策略可以过滤掉会映射到参考文献的污染物,从而减少假阳性比对。我们还表明,我们的方法导致的内源数据损失可以忽略不计,对下游群体遗传学分析没有明显影响。
Filtering out the noise: metagenomic classifiers optimize ancient DNA mapping.
Contamination with exogenous DNA presents a significant challenge in ancient DNA (aDNA) studies of single organisms. Failure to address contamination from microbes, reagents, and present-day sources can impact the interpretation of results. Although field and laboratory protocols exist to limit contamination, there is still a need to accurately distinguish between endogenous and exogenous data computationally. Here, we propose a workflow to reduce exogenous contamination based on a metagenomic classifier. Unlike previous methods that relied exclusively on DNA sequencing reads mapping specificity to a single reference genome to remove contaminating reads, our approach uses Kraken2-based filtering before mapping to the reference genome. Using both simulated and empirical shotgun aDNA data, we show that this workflow presents a simple and efficient method that can be used in a wide range of computational environments-including personal machines. We propose strategies to build specific databases used to profile sequencing data that take into consideration available computational resources and prior knowledge about the target taxa and likely contaminants. Our workflow significantly reduces the overall computational resources required during the mapping process and reduces the total runtime by up to ~94%. The most significant impacts are observed in low endogenous samples. Importantly, contaminants that would map to the reference are filtered out using our strategy, reducing false positive alignments. We also show that our method results in a negligible loss of endogenous data with no measurable impact on downstream population genetics analyses.
期刊介绍:
Briefings in Bioinformatics is an international journal serving as a platform for researchers and educators in the life sciences. It also appeals to mathematicians, statisticians, and computer scientists applying their expertise to biological challenges. The journal focuses on reviews tailored for users of databases and analytical tools in contemporary genetics, molecular and systems biology. It stands out by offering practical assistance and guidance to non-specialists in computerized methodologies. Covering a wide range from introductory concepts to specific protocols and analyses, the papers address bacterial, plant, fungal, animal, and human data.
The journal's detailed subject areas include genetic studies of phenotypes and genotypes, mapping, DNA sequencing, expression profiling, gene expression studies, microarrays, alignment methods, protein profiles and HMMs, lipids, metabolic and signaling pathways, structure determination and function prediction, phylogenetic studies, and education and training.