{"title":"ARMSprimer3: An open-source primer design Python program for amplification refractory mutation system PCR (ARMS-PCR)","authors":"Jingwen Guo , Jeremy Grojean , Huazhang Guo","doi":"10.1016/j.jpi.2025.100442","DOIUrl":null,"url":null,"abstract":"<div><div>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 <span><span>https://github.com/PCRPrimerDesign/ARMSprimer3</span><svg><path></path></svg></span>.</div></div>","PeriodicalId":37769,"journal":{"name":"Journal of Pathology Informatics","volume":"17 ","pages":"Article 100442"},"PeriodicalIF":0.0000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Pathology Informatics","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2153353925000276","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Medicine","Score":null,"Total":0}
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.
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.