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De Novo Draft Genome Assembly Using Fuzzy K-mers

机译:使用模糊K-MERS的DE NOVO草案基因组组装

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Although second generation sequencing technology can be used to rapidly sequence an entire genome, assembly algorithms require a high level of coverage to produce a complete genomic sequence. We describe a fuzzy k-mer approach that is capable of rapidly ordering and orientating low coverage sequence reads with a high level of accuracy. Using this approach, a draft genome of Mycoplasma genitalium, sampled at varying low levels of coverage, was accurately anchored against the genome of Mycoplasma pneumoniae. The anchored reads were assembled into scaffolds with a vastly increased N50 length and an error rate of <1.5%.
机译:尽管第二代排序技术可用于快速序列整个基因组,但组装算法需要高水平的覆盖物以产生完整的基因组序列。我们描述了一种能够快速排序和定向低覆盖序列的模糊K-MER方法,其具有高水平的精度读取。使用这种方法,在不同低水平的覆盖范围内取样的支原体基因产生的草案被精确地固定在支原体肺炎的基因组上。将锚定的读数组装成支架,其N50长度大幅增加,误差率<1.5%。

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