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A long PCR–based approach for DNA enrichment prior to next-generation sequencing for systematic studies

机译:在下一代测序之前进行基于长PCR的DNA富集方法进行系统研究

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摘要

• Premise of the study: We present an alternative approach for molecular systematic studies that combines long PCR and next-generation sequencing. Our approach can be used to generate templates from any DNA source for next-generation sequencing. Here we test our approach by amplifying complete chloroplast genomes, and we present a set of 58 potentially universal primers for angiosperms to do so. Additionally, this approach is likely to be particularly useful for nuclear and mitochondrial regions.• Methods and Results: Chloroplast genomes of 30 species across angiosperms were amplified to test our approach. Amplification success varied depending on whether PCR conditions were optimized for a given taxon. To further test our approach, some amplicons were sequenced on an Illumina HiSeq 2000.• Conclusions: Although here we tested this approach by sequencing plastomes, long PCR amplicons could be generated using DNA from any genome, expanding the possibilities of this approach for molecular systematic studies.
机译:•研究前提:我们为分子系统研究提供了另一种方法,该方法将长PCR和下一代测序相结合。我们的方法可用于从任何DNA来源生成模板,用于下一代测序。在这里,我们通过扩增完整的叶绿体基因组来测试我们的方法,并提出了一组58种潜在的通用被子植物引物。此外,该方法可能对核和线粒体区域特别有用。•方法与结果:扩增了被子植物中30种物种的叶绿体基因组,以测试我们的方法。扩增成功取决于对特定分类群是否优化了PCR条件。为了进一步测试我们的方法,在Illumina HiSeq 2000上对一些扩增子进行了测序。•结论:尽管这里我们通过对质体组测序来测试该方法,但是可以使用任何基因组的DNA生成长PCR扩增子,从而扩大了该方法在分子系统中的可能性。学习。

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