Gorelenkov V, Antipov A, Lejnine S, Daraselia N, Yuryev A
InforMax, Bethesda, MD, USA.
Biotechniques. 2001 Dec;31(6):1326-30. doi: 10.2144/01316bc04.
We have developed a new package of computer programs and algorithms for different PCR applications, including allele-specific PCR, multiplex PCR, and long PCR. The package is included in the upcoming VectorNTI suite software and attempts to incorporate most of the current knowledge about PCR primer design. A wide range of primer characteristics is available for user manipulation to provide improved efficiency and increased flexibility of primer design. To accelerate the primer calculations, we have optimized algorithms using recent advances in computer science such as dynamic trees and lazy evaluation. Proper structural organization of input parameters provides further program acceleration. New Vector NTI primer design software allows calculations of primer pairs for long PCR amplification of 120-kb genomic DNA in 5 min under most stringent input parameters and clustering 435 primer pairs for multiplex PCR within 30 min on a standard Pentium III PC. Our program allows the user to take advantage of molecule annotation by applying different kinds of filtering features during PCR primer design.
我们已经针对不同的PCR应用开发了一套新的计算机程序和算法,包括等位基因特异性PCR、多重PCR和长片段PCR。该软件包包含在即将推出的VectorNTI套件软件中,并尝试纳入目前关于PCR引物设计的大部分知识。用户可以操控多种引物特性,以提高引物设计的效率并增加其灵活性。为了加速引物计算,我们利用计算机科学的最新进展(如动态树和惰性求值)对算法进行了优化。输入参数的合理结构组织进一步加快了程序运行速度。新版Vector NTI引物设计软件能够在最严格的输入参数下,在5分钟内计算出用于长片段PCR扩增120-kb基因组DNA的引物对,并在标准奔腾III计算机上于30分钟内对435对多重PCR引物进行聚类。我们的程序允许用户在PCR引物设计过程中通过应用不同类型的筛选功能来利用分子注释。