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Multiple group-specific sequencing primers for reliable and rapid DNA sequencing.

机译:多种组特异性测序引物,可实现可靠,快速的DNA测序。

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摘要

Pyrosequencing technology is a bioluminometric DNA sequencing method that employs a cascade of four enzymes to deliver sequence signals. To date this technology has been limited to the sequencing of short stretches of DNA. As an improvement to this technique, we have introduced a bacterial group-specific, multiple sequencing primer approach that circumvents sequencing of less informative semi-conservative regions of the 16S rRNA gene. This new approach is suitable for challenging templates, improving sequence data quality, avoiding sequencing of non-specific amplification products, lessening sequencing time, and moreover, this strategy should open the way for many new applications in the future. The group-specific, multiple sequencing primers can be applied in the Sanger dideoxy sequencing method as well. In addition, we have improved the chemistry of the Pyrosequencing system enabling sequencing of longer stretches of DNA, which allows numerous new applications.
机译:焦磷酸测序技术是一种生物发光DNA测序方法,它采用四种酶的级联传递序列信号。迄今为止,该技术仅限于短片段DNA的测序。作为对此技术的改进,我们引入了一种细菌特定组的多重测序引物方法,该方法可绕过16S rRNA基因信息较少的半保守区的测序。这种新方法适用于具有挑战性的模板,提高序列数据质量,避免对非特异性扩增产物进行测序,减少测序时间,此外,该策略应为将来的许多新应用开辟道路。特定于组的多种测序引物也可用于Sanger双脱氧测序方法。此外,我们改进了焦磷酸测序系统的化学性能,可对更长的DNA片段进行测序,从而可以进行许多新的应用。

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