Kalendar Ruslan, Muterko Alexandr, Shamekova Malika, Zhambakin Kabyl
National Center for Biotechnology, 010000, Astana, Kazakhstan.
PrimerDigital Ltd, 00710, Helsinki, Finland.
Methods Mol Biol. 2017;1620:1-31. doi: 10.1007/978-1-4939-7060-5_1.
The polymerase chain reaction (PCR) is fundamental to molecular biology and is the most important practical molecular technique for the research laboratory. The principle of this technique has been further used and applied in plenty of other simple or complex nucleic acid amplification technologies (NAAT). In parallel to laboratory "wet bench" experiments for nucleic acid amplification technologies, in silico or virtual (bioinformatics) approaches have been developed, among which in silico PCR analysis. In silico NAAT analysis is a useful and efficient complementary method to ensure the specificity of primers or probes for an extensive range of PCR applications from homology gene discovery, molecular diagnosis, DNA fingerprinting, and repeat searching. Predicting sensitivity and specificity of primers and probes requires a search to determine whether they match a database with an optimal number of mismatches, similarity, and stability. In the development of in silico bioinformatics tools for nucleic acid amplification technologies, the prospects for the development of new NAAT or similar approaches should be taken into account, including forward-looking and comprehensive analysis that is not limited to only one PCR technique variant. The software FastPCR and the online Java web tool are integrated tools for in silico PCR of linear and circular DNA, multiple primer or probe searches in large or small databases and for advanced search. These tools are suitable for processing of batch files that are essential for automation when working with large amounts of data. The FastPCR software is available for download at http://primerdigital.com/fastpcr.html and the online Java version at http://primerdigital.com/tools/pcr.html .
聚合酶链反应(PCR)是分子生物学的基础,也是研究实验室中最重要的实用分子技术。该技术的原理已在许多其他简单或复杂的核酸扩增技术(NAAT)中得到进一步应用。与核酸扩增技术的实验室“湿实验台”实验并行,已经开发了计算机模拟或虚拟(生物信息学)方法,其中包括计算机模拟PCR分析。计算机模拟NAAT分析是一种有用且高效的补充方法,可确保引物或探针在从同源基因发现、分子诊断、DNA指纹识别和重复序列搜索等广泛的PCR应用中的特异性。预测引物和探针的敏感性和特异性需要进行搜索,以确定它们是否与具有最佳错配数、相似性和稳定性的数据库匹配。在开发用于核酸扩增技术的计算机模拟生物信息学工具时,应考虑新的NAAT或类似方法的发展前景,包括不限于仅一种PCR技术变体的前瞻性和全面分析。FastPCR软件和在线Java网络工具是用于线性和环状DNA的计算机模拟PCR、在大型或小型数据库中进行多个引物或探针搜索以及高级搜索的集成工具。这些工具适用于处理批处理文件,在处理大量数据时,批处理文件对于自动化至关重要。FastPCR软件可从http://primerdigital.com/fastpcr.html下载,在线Java版本可从http://primerdigital.com/tools/pcr.html获取。