ARMSprimer3: An open-source primer design Python program for amplification refractory mutation system PCR (ARMS-PCR)

Q2 Medicine
Jingwen Guo , Jeremy Grojean , Huazhang Guo
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引用次数: 0

Abstract

Single nucleotide polymorphisms (SNPs) are DNA sequence variations of a single base pair. They are the underlying mechanism of most human genetic variation and etiology of many heritable human diseases. SNPs can be reliably detected by amplification refractory mutation system PCR (ARMS-PCR). ARMS-PCR is based on allele-specific PCR primers that only amplify DNA samples with the target allele and do not amplify DNA samples without the target allele. In addition to the allele-specific mismatch at the 3′ end, ARMS-PCR introduces additional deliberate mismatches near the 3′ end of the allele-specific primers to further destabilize the non-specific binding and priming on non-target alleles. This modification increases the specificity for SNP detection, but also increases the complexity of PCR primer design. We developed ARMSprimer3, a Python program to automate the ARMS-PCR primer design process. The validity of ARMSprimer3 was confirmed by successfully using it to develop diagnostic tests in our clinical molecular diagnostic lab. ARMSprimer3 is open-source software and can be freely downloaded from https://github.com/PCRPrimerDesign/ARMSprimer3.
armsprer3:用于扩增难解突变系统PCR (ARMS-PCR)的开源引物设计Python程序
单核苷酸多态性是指单个碱基对的DNA序列变异。它们是大多数人类遗传变异的潜在机制和许多遗传性人类疾病的病因。扩增难解突变系统PCR (ARMS-PCR)可以可靠地检测snp。ARMS-PCR是基于等位基因特异性PCR引物,只扩增带有目标等位基因的DNA样本,而不扩增没有目标等位基因的DNA样本。除了3 ‘端等位基因特异性错配之外,ARMS-PCR在等位基因特异性引物的3 ’端附近引入了额外的故意错配,以进一步破坏非目标等位基因的非特异性结合和引物的稳定性。这种修饰提高了SNP检测的特异性,但也增加了PCR引物设计的复杂性。我们开发了armsprer3,一个Python程序来自动化ARMS-PCR引物设计过程。通过在临床分子诊断实验室成功开发诊断测试,验证了armsprer3的有效性。armsprimer是开源软件,可以从https://github.com/PCRPrimerDesign/ARMSprimer3免费下载。
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来源期刊
Journal of Pathology Informatics
Journal of Pathology Informatics Medicine-Pathology and Forensic Medicine
CiteScore
3.70
自引率
0.00%
发文量
2
审稿时长
18 weeks
期刊介绍: The Journal of Pathology Informatics (JPI) is an open access peer-reviewed journal dedicated to the advancement of pathology informatics. This is the official journal of the Association for Pathology Informatics (API). The journal aims to publish broadly about pathology informatics and freely disseminate all articles worldwide. This journal is of interest to pathologists, informaticians, academics, researchers, health IT specialists, information officers, IT staff, vendors, and anyone with an interest in informatics. We encourage submissions from anyone with an interest in the field of pathology informatics. We publish all types of papers related to pathology informatics including original research articles, technical notes, reviews, viewpoints, commentaries, editorials, symposia, meeting abstracts, book reviews, and correspondence to the editors. All submissions are subject to rigorous peer review by the well-regarded editorial board and by expert referees in appropriate specialties.
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