Daniel G Barber, Harry T Child, Gabrielle R Joslin, Lucy Wierzbicki, Richard K Tennant
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引用次数: 0
摘要
元基因组分析有助于深入了解土壤群落结构和动态。用于元基因组学的长读数测序可以改进分类、基因组组装和功能注释,从而提高微生物生态学的水平。然而,从土壤中纯化高分子量 DNA 的方案尚未得到优化。我们采用统计实验设计方法来提高土壤样本的机械裂解率,从而增加纯化 DNA 片段的长度。在机械裂解过程中输入低能量可提高 DNA 的完整性,从而获得更长的测序读数。与制造商的建议相比,我们的优化设置为 4 m s-1 10 秒,片段长度增加了 70%。低强度裂解产生的更长读数在组装后能产生更长的连续序列,从而可能改善一系列下游分析。重要的是,由于裂解效率的不同,微生物群落组成的偏差极小。因此,我们提出了一个改进从不同土壤类型中纯化的 DNA 片段长度的框架,从而利用长序列测序改进土壤科学研究。
Metagenomic analysis has enabled insights into soil community structure and dynamics. Long-read sequencing for metagenomics can enhance microbial ecology by improving taxonomic classification, genome assembly, and functional annotation. However, protocols for purifying high-molecular weight DNA from soil are not yet optimised. We used a statistical design of experiments approach to enhance mechanical lysis of soil samples, increasing the length of purified DNA fragments. Low energy input into mechanical lysis improved DNA integrity, resulting in longer sequenced reads. Our optimized settings of 4 m s-1 for 10 s increased fragment length by 70% compared to the manufacturer's recommendations. Longer reads from low intensity lysis produced longer contiguous sequences after assembly, potentially improving a range of down-stream analyses. Importantly, there was minimal bias exhibited in the microbial community composition due to lysis efficiency variations. We therefore propose a framework for improving the fragment lengths of DNA purified from diverse soil types, improving soil science research with long-read sequencing.
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