Zhang Ruifang, Zhu Zanhua, Zhu Hongming, Nguyen Tu, Yao Fengxia, Xia Kun, Liang Desheng, Liu Chunyu
National Laboratory of Medical Genetics of China, Central South University Changsha, Hunan, People's Republic of China.
Nucleic Acids Res. 2005 Jul 1;33(Web Server issue):W489-92. doi: 10.1093/nar/gki358.
The Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) is a relatively simple and inexpensive method for genotyping single nucleotide polymorphisms (SNPs). It requires minimal investment in instrumentation. Here, we describe a web application, 'SNP Cutter,' which designs PCR-RFLP assays on a batch of SNPs from the human genome. NCBI dbSNP rs IDs or formatted SNPs are submitted into the SNP Cutter which then uses restriction enzymes from a pre-selected list to perform enzyme selection. The program is capable of designing primers for either natural PCR-RFLP or mismatch PCR-RFLP, depending on the SNP sequence data. SNP Cutter generates the information needed to evaluate and perform genotyping experiments, including a PCR primers list, sizes of original amplicons and different allelic fragment after enzyme digestion. Some output data is tab-delimited, therefore suitable for database archiving. The SNP Cut-ter is available at http://bioinfo.bsd.uchicago.edu/SNP_cutter.htm.
聚合酶链反应-限制性片段长度多态性(PCR-RFLP)是一种用于对单核苷酸多态性(SNP)进行基因分型的相对简单且成本低廉的方法。它在仪器设备方面所需的投入极少。在此,我们描述一个网络应用程序“SNP Cutter”,它可针对一批来自人类基因组的SNP设计PCR-RFLP分析方法。将NCBI dbSNP rs ID或格式化的SNP提交给“SNP Cutter”,然后它会使用预先选定列表中的限制性内切酶进行酶的选择。该程序能够根据SNP序列数据为天然PCR-RFLP或错配PCR-RFLP设计引物。“SNP Cutter”生成评估和进行基因分型实验所需的信息,包括PCR引物列表、原始扩增子的大小以及酶切后不同等位基因片段的大小。一些输出数据是以制表符分隔的,因此适合存档到数据库。可通过http://bioinfo.bsd.uchicago.edu/SNP_cutter.htm获取“SNP Cutter”。