Wangkumhang Pongsakorn, Chaichoompu Kridsadakorn, Ngamphiw Chumpol, Ruangrit Uttapong, Chanprasert Juntima, Assawamakin Anunchai, Tongsima Sissades
Biostatistics and Informatics Laboratory, Genomics Institute, National Center for Genetic Engineering and Biotechnology, Thailand Science Park, Pathumtani, Thailand.
BMC Genomics. 2007 Aug 14;8:275. doi: 10.1186/1471-2164-8-275.
Allele-specific (AS) Polymerase Chain Reaction is a convenient and inexpensive method for genotyping Single Nucleotide Polymorphisms (SNPs) and mutations. It is applied in many recent studies including population genetics, molecular genetics and pharmacogenomics. Using known AS primer design tools to create primers leads to cumbersome process to inexperience users since information about SNP/mutation must be acquired from public databases prior to the design. Furthermore, most of these tools do not offer the mismatch enhancement to designed primers. The available web applications do not provide user-friendly graphical input interface and intuitive visualization of their primer results.
This work presents a web-based AS primer design application called WASP. This tool can efficiently design AS primers for human SNPs as well as mutations. To assist scientists with collecting necessary information about target polymorphisms, this tool provides a local SNP database containing over 10 million SNPs of various populations from public domain databases, namely NCBI dbSNP, HapMap and JSNP respectively. This database is tightly integrated with the tool so that users can perform the design for existing SNPs without going off the site. To guarantee specificity of AS primers, the proposed system incorporates a primer specificity enhancement technique widely used in experiment protocol. In particular, WASP makes use of different destabilizing effects by introducing one deliberate 'mismatch' at the penultimate (second to last of the 3'-end) base of AS primers to improve the resulting AS primers. Furthermore, WASP offers graphical user interface through scalable vector graphic (SVG) draw that allow users to select SNPs and graphically visualize designed primers and their conditions.
WASP offers a tool for designing AS primers for both SNPs and mutations. By integrating the database for known SNPs (using gene ID or rs number), this tool facilitates the awkward process of getting flanking sequences and other related information from public SNP databases. It takes into account the underlying destabilizing effect to ensure the effectiveness of designed primers. With user-friendly SVG interface, WASP intuitively presents resulting designed primers, which assist users to export or to make further adjustment to the design. This software can be freely accessed at http://bioinfo.biotec.or.th/WASP.
等位基因特异性(AS)聚合酶链反应是一种用于对单核苷酸多态性(SNP)和突变进行基因分型的便捷且廉价的方法。它被应用于许多近期的研究中,包括群体遗传学、分子遗传学和药物基因组学。使用已知的AS引物设计工具来创建引物,对于缺乏经验的用户来说过程繁琐,因为在设计之前必须从公共数据库获取有关SNP/突变的信息。此外,这些工具中的大多数都没有为设计的引物提供错配增强功能。现有的网络应用程序没有提供用户友好的图形输入界面以及引物结果的直观可视化。
这项工作展示了一个基于网络的AS引物设计应用程序,称为WASP。该工具可以有效地为人类SNP以及突变设计AS引物。为了帮助科学家收集有关目标多态性的必要信息,该工具提供了一个本地SNP数据库,其中包含分别来自公共领域数据库(即NCBI dbSNP、HapMap和JSNP)的超过1000万个不同人群的SNP。该数据库与工具紧密集成,以便用户无需离开该网站即可对现有SNP进行设计。为了保证AS引物的特异性,所提出的系统纳入了一种在实验方案中广泛使用的引物特异性增强技术。具体而言,WASP通过在AS引物的倒数第二个(3'端的倒数第二个)碱基处引入一个故意的“错配”来利用不同的去稳定化效应,以改进所得的AS引物。此外,WASP通过可缩放矢量图形(SVG)绘图提供图形用户界面,允许用户选择SNP并以图形方式可视化设计的引物及其条件。
WASP提供了一种为SNP和突变设计AS引物的工具。通过整合已知SNP的数据库(使用基因ID或rs编号),该工具简化了从公共SNP数据库获取侧翼序列和其他相关信息的繁琐过程。它考虑了潜在的去稳定化效应,以确保设计引物的有效性。通过用户友好的SVG界面,WASP直观地展示所得的设计引物,帮助用户导出或对设计进行进一步调整。该软件可在http://bioinfo.biotec.or.th/WASP上免费访问。