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NGS-PrimerPlex:高通量多重聚合酶链反应引物设计。

NGS-PrimerPlex: High-throughput primer design for multiplex polymerase chain reactions.

机构信息

Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russia.

Novosibirsk State University, Novosibirsk, Russia.

出版信息

PLoS Comput Biol. 2020 Dec 30;16(12):e1008468. doi: 10.1371/journal.pcbi.1008468. eCollection 2020 Dec.

DOI:10.1371/journal.pcbi.1008468
PMID:33378360
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7802936/
Abstract

Multiplex polymerase chain reaction (PCR) has multiple applications in molecular biology, including developing new targeted next-generation sequencing (NGS) panels. We present NGS-PrimerPlex, an efficient and versatile command-line application that designs primers for different refined types of amplicon-based genome target enrichment. It supports nested and anchored multiplex PCR, redistribution among multiplex reactions of primers constructed earlier, and extension of existing NGS-panels. The primer design process takes into consideration the formation of secondary structures, non-target amplicons between all primers of a pool, primers and high-frequent genome single-nucleotide polymorphisms (SNPs) overlapping. Moreover, users of NGS-PrimerPlex are free from manually defining input genome regions, because it can be done automatically from a list of genes or their parts like exon or codon numbers. Using the program, the NGS-panel for sequencing the LRRK2 gene coding regions was created, and 354 DNA samples were studied successfully with a median coverage of 97.4% of target regions by at least 30 reads. To show that NGS-PrimerPlex can also be applied for bacterial genomes, we designed primers to detect foodborne pathogens Salmonella enterica, Escherichia coli O157:H7, Listeria monocytogenes, and Staphylococcus aureus considering variable positions of the genomes.

摘要

多重聚合酶链反应(PCR)在分子生物学中有多种应用,包括开发新的靶向下一代测序(NGS)面板。我们介绍了 NGS-PrimerPlex,这是一种高效且通用的命令行应用程序,可用于设计基于扩增子的基因组靶向富集的不同细化类型的引物。它支持嵌套和锚定多重 PCR、先前构建的引物在多重反应中的重新分配,以及现有 NGS 面板的扩展。引物设计过程考虑了二级结构的形成、池中的所有引物之间的非靶标扩增子、引物和高频基因组单核苷酸多态性(SNP)重叠。此外,NGS-PrimerPlex 的用户无需手动定义输入基因组区域,因为它可以从基因列表或其部分(如外显子或密码子编号)自动完成。使用该程序创建了用于测序 LRRK2 基因编码区的 NGS 面板,并成功研究了 354 个 DNA 样本,目标区域的中位数覆盖率至少为 30 个读数的 97.4%。为了表明 NGS-PrimerPlex 也可用于细菌基因组,我们设计了引物以检测食源性病原体沙门氏菌、大肠杆菌 O157:H7、李斯特菌和金黄色葡萄球菌,同时考虑到基因组的可变位置。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54bd/7802936/8a968c6c0b77/pcbi.1008468.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54bd/7802936/81c702576dbf/pcbi.1008468.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54bd/7802936/b2b98b8b2444/pcbi.1008468.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54bd/7802936/86ced3c4b926/pcbi.1008468.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54bd/7802936/8a968c6c0b77/pcbi.1008468.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54bd/7802936/81c702576dbf/pcbi.1008468.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54bd/7802936/b2b98b8b2444/pcbi.1008468.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54bd/7802936/86ced3c4b926/pcbi.1008468.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54bd/7802936/8a968c6c0b77/pcbi.1008468.g004.jpg

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