Chang Hsueh-Wei, Chuang Li-Yeh, Cheng Yu-Huei, Hung Yu-Chen, Wen Cheng-Hao, Gu De-Leung, Yang Cheng-Hong
Department of Biomedical Science and Environmental Biology, Kaohsiung Medical University, Taiwan.
Biotechniques. 2009 May;46(6):421-31. doi: 10.2144/000113092.
Many kinds of primer design (PD) software tools have been developed, but most of them lack a single nucleotide polymorphism (SNP) genotyping service. Here, we introduce the web-based freeware "Prim-SNPing," which, in addition to general PD, provides three kinds of primer design functions for cost-effective SNP genotyping: natural PD, mutagenic PD, and confronting two-pair primers (CTPP) PD. The natural PD and mutagenic PD provide primers and restriction enzyme mining for polymerase chain reaction-restriction fragment of length polymorphism (PCR-RFLP), while CTPP PD provides primers for restriction enzyme-free SNP genotyping. The PCR specificity and efficiency of the designed primers are improved by BLAST searching and evaluating secondary structure (such as GC clamps, dimers, and hairpins), respectively. The length pattern of PCR-RFLP using natural PD is user-adjustable, and the restriction sites of the RFLP enzymes provided by Prim-SNPing are confirmed to be absent within the generated PCR product. In CTPP PD, the need for a separate digestion step in RFLP is eliminated, thus making it faster and cheaper. The output of Prim-SNPing includes the primer list, melting temperature (Tm) value, GC percentage, and amplicon size with enzyme digestion information. The reference SNP (refSNP, or rs) clusters from the Single Nucleotide Polymorphism database (dbSNP) at the National Center for Biotechnology Information (NCBI), and multiple other formats of human, mouse, and rat SNP sequences are acceptable input. In summary, Prim-SNPing provides interactive, user-friendly and cost-effective primer design for SNP genotyping. It is freely available at http://bio.kuas.edu.tw/prim-snping.
人们已经开发了多种引物设计(PD)软件工具,但其中大多数都缺乏单核苷酸多态性(SNP)基因分型服务。在此,我们介绍基于网络的免费软件“Prim-SNPing”,它除了常规的引物设计外,还提供三种用于经济高效SNP基因分型的引物设计功能:自然引物设计、诱变引物设计和双引物对(CTPP)引物设计。自然引物设计和诱变引物设计为聚合酶链反应-限制性片段长度多态性(PCR-RFLP)提供引物和限制性酶挖掘,而CTPP引物设计为无限制性酶的SNP基因分型提供引物。通过BLAST搜索和评估二级结构(如GC夹、二聚体和发夹结构)分别提高了所设计引物的PCR特异性和效率。使用自然引物设计的PCR-RFLP的长度模式可由用户调整,并且确认Prim-SNPing提供的RFLP酶的限制性位点在所生成的PCR产物中不存在。在CTPP引物设计中,消除了RFLP中单独消化步骤的需要,从而使其更快且更便宜。Prim-SNPing的输出包括引物列表、熔解温度(Tm)值、GC百分比以及带有酶切信息的扩增子大小。来自美国国立生物技术信息中心(NCBI)的单核苷酸多态性数据库(dbSNP)的参考SNP(refSNP,或rs)簇以及人类、小鼠和大鼠SNP序列的多种其他格式都是可接受的输入。总之,Prim-SNPing为SNP基因分型提供了交互式、用户友好且经济高效的引物设计。可在http://bio.kuas.edu.tw/prim-snping免费获取。