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BatchPrimer3: A high throughput web application for PCR and sequencing primer design

机译:BatchPrimer3:用于PCR和测序引物设计的高通量Web应用程序

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Background Microsatellite (simple sequence repeat – SSR) and single nucleotide polymorphism (SNP) markers are two types of important genetic markers useful in genetic mapping and genotyping. Often, large-scale genomic research projects require high-throughput computer-assisted primer design. Numerous such web-based or standard-alone programs for PCR primer design are available but vary in quality and functionality. In particular, most programs lack batch primer design capability. Such a high-throughput software tool for designing SSR flanking primers and SNP genotyping primers is increasingly demanded. Results A new web primer design program, BatchPrimer3, is developed based on Primer3. BatchPrimer3 adopted the Primer3 core program as a major primer design engine to choose the best primer pairs. A new score-based primer picking module is incorporated into BatchPrimer3 and used to pick position-restricted primers. BatchPrimer3 v1.0 implements several types of primer designs including generic primers, SSR primers together with SSR detection, and SNP genotyping primers (including single-base extension primers, allele-specific primers, and tetra-primers for tetra-primer ARMS PCR), as well as DNA sequencing primers. DNA sequences in FASTA format can be batch read into the program. The basic information of input sequences, as a reference of parameter setting of primer design, can be obtained by pre-analysis of sequences. The input sequences can be pre-processed and masked to exclude and/or include specific regions, or set targets for different primer design purposes as in Primer3Web and primer3Plus. A tab-delimited or Excel-formatted primer output also greatly facilitates the subsequent primer-ordering process. Thousands of primers, including wheat conserved intron-flanking primers, wheat genome-specific SNP genotyping primers, and Brachypodium SSR flanking primers in several genome projects have been designed using the program and validated in several laboratories. Conclusion BatchPrimer3 is a comprehensive web primer design program to develop different types of primers in a high-throughput manner. Additional methods of primer design can be easily integrated into future versions of BatchPrimer3. The program with source code and thousands of PCR and sequencing primers designed for wheat and Brachypodium are accessible at http://wheat.pw.usda.gov/demos/BatchPrimer3/ .
机译:背景微卫星(简单序列重复-SSR)和单核苷酸多态性(SNP)标记是可用于遗传作图和基因分型的两种重要遗传标记。通常,大规模的基因组研究项目需要高通量计算机辅助引物设计。可使用许多此类基于Web或标准的程序来进行PCR引物设计,但它们的质量和功能各不相同。特别是,大多数程序缺少批处理引物设计功能。越来越需要用于设计SSR侧翼引物和SNP基因分型引物的高通量软件工具。结果基于Primer3,开发了一个新的Web底漆设计程序BatchPrimer3。 BatchPrimer3采用Primer3核心程序作为主要的引物设计引擎,以选择最佳的引物对。 BatchPrimer3中集成了一个新的基于分数的引物选择模块,用于选择位置受限的引物。 BatchPrimer3 v1.0实现了几种引物设计,包括通用引物,SSR引物和SSR检测以及SNP基因分型引物(包括单碱基延伸引物,等位基因特异性引物和用于四引物ARMS PCR的四引物),以及DNA测序引物。可以将FASTA格式的DNA序列批量读取到程序中。输入序列的基本信息可以作为引物设计参数设置的参考,可以通过序列的预先分析获得。可以对输入序列进行预处理和屏蔽,以排除和/或包括特定区域,或为Primer3Web和primer3Plus中的不同引物设计目的设置目标。制表符分隔或Excel格式的引物输出也极大地方便了随后的引物排序过程。使用该程序设计了数千个引物,包括小麦保守的内含子侧翼引物,小麦基因组特异性SNP基因分型引物和短臂孢子SSR侧翼引物,并在多个实验室中进行了验证。结论BatchPrimer3是一个全面的Web引物设计程序,可以以高通量方式开发不同类型的引物。引物设计的其他方法可以轻松地集成到BatchPrimer3的未来版本中。可通过http://wheat.pw.usda.gov/demos/BatchPrimer3/访问该程序,该程序带有源代码以及数千个针对小麦和短茎线虫的PCR和测序引物。

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