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De novo genome sequence assembly of a filamentous fungus using Sanger, 454 and Illumina sequence data

机译:使用Sanger,454和Illumina序列数据进行丝状真菌的从头基因组序列组装

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ABSTRACT: Sequencing-by-synthesis technologies can reduce the cost of generating de novo genome assemblies. We report a method for assembling draft genome sequences of eukaryotic organisms that integrates sequence information from different sources, and demonstrate its effectiveness by assembling a ~32.5 Mb draft genome sequence for the forest pathogen Grosmannia clavigera, an ascomycete fungus. We also developed a method for assessing draft assemblies using Illumina paired end read data and demonstrate how we are using it to guide future sequence finishing. Our results demonstrate that eukaryotic genome sequences can be accurately assembled by combining Illumina, 454 and Sanger sequence data.
机译:摘要:合成测序技术可以降低产生从头基因组装配的成本。我们报告了一种方法,它整合了来自不同来源的序列信息,整合了真核生物的基因组草稿序列,并通过组装〜32.5 Mb的草木病原体罗汉果,一种子囊真菌,证明了其有效性。我们还开发了一种使用Illumina配对末端读取数据评估草图装配的方法,并演示了如何使用它来指导将来的序列完成。我们的结果表明,通过结合Illumina,454和Sanger序列数据可以准确地组装真核生物基因组序列。

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