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An Effective Pipeline Based on Relative Coverage for the Genome Assembly of Phytoplasmas and Other Fastidious Prokaryotes

机译:一种基于相对覆盖度的有效方法来检测植物原虫和其他优良原核生物的基因组组装

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Background For the plant pathogenic phytoplasmas, as well as for several fastidious prokaryotes, axenic cultivation is extremely difficult or not possible yet; therefore, even with second generation sequencing methods, obtaining the sequence of their genomes is challenging due to host sequence contamination. Objective With the Phytoassembly pipeline here presented, we aim to provide a method to obtain high quality genome drafts for the phytoplasmas and other uncultivable plant pathogens, by exploiting the coverage differential in the ILLUMINA sequences from the pathogen and the host, and using the sequencing of a healthy, isogenic plant as a filter. Validation The pipeline has been benchmarked using simulated and real ILLUMINA runs from phytoplasmas whose genome is known, and it was then used to obtain high quality drafts for three new phytoplasma genomes. Conclusion For phytoplasma infected samples containing &2-4% of pathogen DNA and an isogenic reference healthy sample, the resulting assemblies can be next to complete. The Phytoassembly source code is available on GitHub at https://github.com/cpolano/phytoassembly .
机译:背景技术对于植物病原体质原体以及一些有营养的原核生物来说,过氧化物酶的培养极为困难或尚不可能。因此,即使采用第二代测序方法,由于宿主序列的污染,获得其基因组的序列也是具有挑战性的。目的通过本文介绍的植物组装管道,我们旨在提供一种方法,通过利用病原体和宿主的ILLUMINA序列的覆盖差异,并利用植物的测序方法来获得植物原质和其他不可栽培植物病原体的高质量基因组草图。健康的等基因植物作为过滤器。验证该管道已使用模拟和真实ILLUMINA进行了基准测试,该运行来自已知基因组的植物原质,然后用​​于获得三个新植物原质基因组的高质量草图。结论对于包含> 2-4%的病原体DNA的被质体感染的样品和等基因的参考健康样品,所得的组装可以接近完成。 Phytoassembly源代码可从GitHub上的https://github.com/cpolano/phytoassembly获得。

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