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Individual genome assembly from complex community short-read metagenomic datasets

机译:来自复杂社区的短基因组学数据集的单个基因组组装

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摘要

Assembling individual genomes from complex community metagenomic data remains a challenging issue for environmental studies. We evaluated the quality of genome assemblies from community short read data (Illumina 100 bp pair-ended sequences) using datasets recovered from freshwater and soil microbial communities as well as in silico simulations. Our analyses revealed that the genome of a single genotype (or species) can be accurately assembled from a complex metagenome when it shows at least about 20 × coverage. At lower coverage, however, the derived assemblies contained a substantial fraction of non-target sequences (chimeras), which explains, at least in part, the higher number of hypothetical genes recovered in metagenomic relative to genomic projects. We also provide examples of how to detect intrapopulation structure in metagenomic datasets and estimate the type and frequency of errors in assembled genes and contigs from datasets of varied species complexity.
机译:从复杂的社区宏基因组学数据组装单个基因组对于环境研究仍然是一个具有挑战性的问题。我们使用从淡水和土壤微生物群落中回收的数据集以及计算机模拟,从群落短读数据(Illumina 100 bp对末端序列)评估了基因组装配的质量。我们的分析表明,当单个基因型(或物种)的基因组显示至少约20倍的覆盖率时,它可以从复杂的基因组中准确组装。但是,在较低的覆盖率下,衍生的程序集包含相当一部分非靶序列(嵌合体),这至少部分地解释了相对于基因组计划,在宏基因组学中回收的假想基因数量更高。我们还提供了一些示例,说明如何在宏基因组数据集中检测种群内结构,并根据各种物种复杂性的数据集估算组装基因和重叠群中错误的类型和频率。

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