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擎天柱引物:用于人类外显子区域下一代测序的PCR富集引物设计程序。

Optimus Primer: A PCR enrichment primer design program for next-generation sequencing of human exonic regions.

作者信息

Brown Andrew Mk, Lo Ken Sin, Guelpa Paul, Beaudoin Mélissa, Rioux John D, Tardif Jean-Claude, Phillips Michael S, Lettre Guillaume

机构信息

Université de Montréal, Montreal, Quebec, Canada.

出版信息

BMC Res Notes. 2010 Jul 7;3:185. doi: 10.1186/1756-0500-3-185.

Abstract

BACKGROUND

Polymerase chain reaction (PCR) remains a simple, flexible, and inexpensive method for enriching genomic regions of interest for next-generation sequencing. In order to utilize PCR in this context, a major challenge facing researchers is how to generate a very large number of functional PCR primers that will successfully generate useable amplicons. For instance, in an exon-only re-sequencing project targeting 100 genes, each with 10 exons, 1,000 pairs of primers are required. In fact, the reality is often more complex as each gene might have several isoforms and large exons need to be divided to maintain the desired amplicon size. With only a list of gene names, our program Optimus Primer (OP) automatically takes into account all these variables, and can generate primers with no need to provide genome coordinates. More importantly however, OP, unlike other primer design programs, uniquely utilizes Primer3 in an iterative manner that allows the user to progressively design up to four iterations of primer designs. Through a single interface, the user can specify up to four different design parameters with different stringencies, thus increasing the probability that a functional PCR primer pair will be designed for all regions of interest in a single pass of the pipeline.

FINDINGS

To demonstrate the effectiveness of the program, we designed PCR primers against 77 genes located in loci associated with ulcerative colitis as part of a candidate gene re-sequencing experiment. We achieved an experimental success rate of 93% or 472 out of 508 amplicons spanning the exonic regions of the 77 genes. Moreover, by automatically passing amplicons that failed primer design through three additional iterations of design parameters, we achieved an additional 170 successful primer pairs or 34% more in a single pass of OP than by conventional methods.

CONCLUSION

With only a gene list and PCR parameters, a user can produce hundreds of PCR primer designs for regions of interest with a high probability of success in a very short amount of time. Optimus Primer is an essential tool for researchers who want to pursue PCR-based enrichment strategies for next-generation re-sequencing applications. The program can be accessed via website at http://op.pgx.ca.

摘要

背景

聚合酶链反应(PCR)仍然是一种简单、灵活且廉价的方法,用于为下一代测序富集感兴趣的基因组区域。为了在这种情况下使用PCR,研究人员面临的一个主要挑战是如何生成大量能够成功产生可用扩增子的功能性PCR引物。例如,在一个仅针对外显子的重测序项目中,目标是100个基因,每个基因有10个外显子,则需要1000对引物。实际上,情况往往更复杂,因为每个基因可能有几种异构体,并且大的外显子需要分割以维持所需的扩增子大小。仅通过基因名称列表,我们的程序Optimus Primer(OP)会自动考虑所有这些变量,并且无需提供基因组坐标即可生成引物。然而,更重要的是,与其他引物设计程序不同,OP独特地以迭代方式使用Primer3,允许用户逐步设计多达四轮引物设计。通过单个界面,用户可以指定多达四个具有不同严格程度的不同设计参数,从而增加在流水线的单次运行中为所有感兴趣区域设计出功能性PCR引物对的概率。

研究结果

为了证明该程序的有效性,作为候选基因重测序实验的一部分,我们针对位于与溃疡性结肠炎相关位点的77个基因设计了PCR引物。我们在跨越这77个基因外显子区域的508个扩增子中获得了93%或472个的实验成功率。此外,通过自动将引物设计失败的扩增子通过另外三轮设计参数,我们在OP的单次运行中比传统方法又获得了170个成功的引物对,即多出34%。

结论

仅通过基因列表和PCR参数,用户就能在极短时间内以高成功率为感兴趣的区域生成数百个PCR引物设计。Optimus Primer是希望为下一代重测序应用采用基于PCR的富集策略的研究人员的必备工具。该程序可通过网站http://op.pgx.ca访问。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa72/2916007/7755d72501b2/1756-0500-3-185-1.jpg

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