{"title":"V-primer: software for the efficient design of genome-wide InDel and SNP markers from multi-sample variant call format (VCF) genotyping data.","authors":"Satoshi Natsume, Kaori Oikawa, Chihiro Nomura, Kazue Ito, Hiroe Utsushi, Motoki Shimizu, Ryohei Terauchi, Akira Abe","doi":"10.1270/jsbbs.23018","DOIUrl":null,"url":null,"abstract":"<p><p>DNA markers are indispensable tools in genetics and genomics research as well as in crop breeding, particularly for marker-assisted selection. Recent advances in next-generation sequencing technology have made it easier to obtain genome sequences for various crop species, enabling the large-scale identification of DNA polymorphisms among varieties, which in turn has made DNA marker design more accessible. However, existing primer design software is not suitable for designing many types of genome-wide DNA markers from next-generation sequencing data. Here, we describe the development of V-primer, high-throughput software for designing insertion/deletion, cleaved amplified polymorphic sequence, and single-nucleotide polymorphism (SNP) markers. We validated the applicability of these markers in different crops. In addition, we performed multiplex PCR targeted amplicon sequencing using SNP markers designed with V-primer. Our results demonstrate that V-primer facilitates the efficient and accurate design of primers and is thus a useful tool for genetics, genomics, and crop breeding. V-primer is freely available at https://github.com/ncod3/vprimer.</p>","PeriodicalId":9258,"journal":{"name":"Breeding Science","volume":"1 1","pages":"415-420"},"PeriodicalIF":2.0000,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10722093/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Breeding Science","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1270/jsbbs.23018","RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/9/9 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"AGRONOMY","Score":null,"Total":0}
引用次数: 0
Abstract
DNA markers are indispensable tools in genetics and genomics research as well as in crop breeding, particularly for marker-assisted selection. Recent advances in next-generation sequencing technology have made it easier to obtain genome sequences for various crop species, enabling the large-scale identification of DNA polymorphisms among varieties, which in turn has made DNA marker design more accessible. However, existing primer design software is not suitable for designing many types of genome-wide DNA markers from next-generation sequencing data. Here, we describe the development of V-primer, high-throughput software for designing insertion/deletion, cleaved amplified polymorphic sequence, and single-nucleotide polymorphism (SNP) markers. We validated the applicability of these markers in different crops. In addition, we performed multiplex PCR targeted amplicon sequencing using SNP markers designed with V-primer. Our results demonstrate that V-primer facilitates the efficient and accurate design of primers and is thus a useful tool for genetics, genomics, and crop breeding. V-primer is freely available at https://github.com/ncod3/vprimer.
V-primer:从多样本变异调用格式(VCF)基因分型数据中高效设计全基因组 InDel 和 SNP 标记的软件。
DNA 标记是遗传学和基因组学研究以及作物育种不可或缺的工具,尤其是在标记辅助选择方面。近年来,下一代测序技术的发展使得获取各种作物物种的基因组序列变得更加容易,从而可以大规模鉴定品种间的 DNA 多态性,这反过来又使 DNA 标记的设计变得更加容易。然而,现有的引物设计软件并不适合从新一代测序数据中设计多种类型的全基因组 DNA 标记。在此,我们介绍了 V-primer 的开发情况,这是一款用于设计插入/缺失、裂解扩增多态性序列和单核苷酸多态性(SNP)标记的高通量软件。我们验证了这些标记在不同作物中的适用性。此外,我们还使用 V-primer 设计的 SNP 标记进行了多重 PCR 目标扩增片段测序。我们的研究结果表明,V-primer 可以高效、准确地设计引物,因此是遗传学、基因组学和作物育种的有用工具。V-primer 可在 https://github.com/ncod3/vprimer 免费获取。
期刊介绍:
Breeding Science is published by the Japanese Society of Breeding. Breeding Science publishes research papers, notes and reviews
related to breeding. Research Papers are standard original articles.
Notes report new cultivars, breeding lines, germplasms, genetic
stocks, mapping populations, database, software, and techniques
significant and useful for breeding. Reviews summarize recent and
historical events related breeding.
Manuscripts should be submitted by corresponding author. Corresponding author must have obtained permission from all authors
prior to submission. Correspondence, proofs, and charges of excess page and color figures should be handled by the corresponding author.