一种改进的自然PCR-RFLP引物设计方法

Li-Yeh Chuang, Yu-Da Lin, Hsueh-Wei Chang, Cheng-Hong Yang
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引用次数: 0

摘要

聚合酶链反应限制性片段长度多态性(PCR-RFLP)技术常用于实验室和许多与单核苷酸多态性(SNP)相关的复杂遗传疾病的基础研究。在进行PCR-RFLP SNP基因分型时,可行的引物对受到许多限制,并且需要限制性内切酶来区分目标SNP。在本研究中,我们开发了一种基于粒子群优化算法的自然PCR-RFLP引物设计方法,用于SNP基因分型。SLC6A4基因的单核苷酸多态性的计算机模拟表明,该方法可靠地设计出最适合常见引物约束的天然PCR-RFLP引物,并识别出可用的限制性内切酶。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An Improved Natural PCR-RFLP Primer Design Method
The polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP) technique is often used in laboratories and many basic research studies of complex genetic diseases associated with single nucleotide polymorphisms (SNP). When performing PCR-RFLP for SNP genotyping, feasible primer pairs are subject to numerous constraints and require a restriction enzyme for discriminating the target SNP. In this study, we develop a method for natural PCR-RFLP primer design for SNP genotyping using a particle swarm optimization algorithm. The in silico simulation with SNPs of the SLC6A4 gene demonstrates that this method reliably produces designs for natural PCR-RFLP primers which best fit the common primer constraints and also identifies available restriction enzymes.
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