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Novel computational methods for increasing PCR primer design effectiveness in directed sequencing

机译:在定向测序中提高PCR引物设计效率的新型计算方法

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Background Polymerase chain reaction (PCR) is used in directed sequencing for the discovery of novel polymorphisms. As the first step in PCR directed sequencing, effective PCR primer design is crucial for obtaining high-quality sequence data for target regions. Since current computational primer design tools are not fully tuned with stable underlying laboratory protocols, researchers may still be forced to iteratively optimize protocols for failed amplifications after the primers have been ordered. Furthermore, potentially identifiable factors which contribute to PCR failures have yet to be elucidated. This inefficient approach to primer design is further intensified in a high-throughput laboratory, where hundreds of genes may be targeted in one experiment. Results We have developed a fully integrated computational PCR primer design pipeline that plays a key role in our high-throughput directed sequencing pipeline. Investigators may specify target regions defined through a rich set of descriptors, such as Ensembl accessions and arbitrary genomic coordinates. Primer pairs are then selected computationally to produce a minimal amplicon set capable of tiling across the specified target regions. As part of the tiling process, primer pairs are computationally screened to meet the criteria for success with one of two PCR amplification protocols. In the process of improving our sequencing success rate, which currently exceeds 95% for exons, we have discovered novel and accurate computational methods capable of identifying primers that may lead to PCR failures. We reveal the laboratory protocols and their associated, empirically determined computational parameters, as well as describe the novel computational methods which may benefit others in future primer design research. Conclusion The high-throughput PCR primer design pipeline has been very successful in providing the basis for high-quality directed sequencing results and for minimizing costs associated with labor and reprocessing. The modular architecture of the primer design software has made it possible to readily integrate additional primer critique tests based on iterative feedback from the laboratory. As a result, the primer design software, coupled with the laboratory protocols, serves as a powerful tool for low and high-throughput primer design to enable successful directed sequencing.
机译:背景技术聚合酶链反应(PCR)用于直接测序中,以发现新的多态性。作为PCR定向测序的第一步,有效的PCR引物设计对于获得目标区域的高质量序列数据至关重要。由于目前的计算引物设计工具尚未完全通过稳定的基础实验室规程进行调整,因此在订购引物后,研究人员可能仍被迫迭代优化扩增失败的规程。此外,尚未阐明导致PCR失败的潜在可识别因素。这种高效率的引物设计方法在高通量实验室中得到了进一步加强,该实验室可以在一个实验中靶向数百个基因。结果我们开发了一个完全集成的计算PCR引物设计管线,该管线在我们的高通量定向测序管线中起着关键作用。研究人员可以指定通过丰富的描述符集定义的目标区域,例如Ensembl入藏和任意基因组坐标。然后通过计算选择引物对,以产生最小的扩增子集,该扩增子集能够在指定的目标区域内平铺。作为切片过程的一部分,对引物对进行计算筛选,以符合两种PCR扩增方案之一的成功标准。在提高测序成功率(目前外显子超过95%)的过程中,我们发现了新颖,准确的计算方法,能够识别可能导致PCR失败的引物。我们揭示了实验室规程及其相关的,凭经验确定的计算参数,并描述了可能在未来引物设计研究中受益的新颖计算方法。结论高通量PCR引物设计流程非常成功,为高质量的定向测序结果提供了基础,并最大程度地减少了与人工和后处理相关的成本。引物设计软件的模块化体系结构使基于实验室的反复反馈,可以轻松地集成其他引物评论测试。因此,引物设计软件与实验室规程结合在一起,可作为低通量和高通量引物设计的强大工具,从而能够成功进行定向测序。

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