• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

一种用于 SARS-CoV-2 PCR 引物设计的保守序列提取新方法,具有前瞻性突变预测。

A novel method for conserved sequence extraction with prospective mutation prediction for SARS-CoV-2 PCR primer design.

机构信息

Izmir University of Economics, Faculty of Engineering, Department of Biomedical Engineering, Izmir, Turkey.

Kocaeli University, Faculty of Medicine, Clinical Laboratory, PCR Unit, Kocaeli, Turkey; Turkish Republic of Northern Cyprus.

出版信息

J Virol Methods. 2021 Jul;293:114146. doi: 10.1016/j.jviromet.2021.114146. Epub 2021 Apr 1.

DOI:10.1016/j.jviromet.2021.114146
PMID:33812944
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8015351/
Abstract

While the whole genomic sequence of SARS-CoV-2 had been revealed, it was also demonstrated that the genome of SARS-CoV-2 exhibits identity with the genome of SARS-CoV and MERS-CoV with ratios of 80 % and 50 % respectively. In the light of SARS-CoV-2 infection and mortality data, diagnosis and treatment of COVID-19 came into prominence around the world. As such many RT-PCR kits have been developed by biotechnology scientists. However viruses are fast mutating organisms and in order to increase accuracy, feasibility in long term and avoid the off target results of RT-PCR assays, regions of viral genome with low mutation rate and designing of primers targeting these regions are quite important. In this scope, we are presenting a novel algorithm that could be used for finding low mutation rate regions of SARS-CoV-2 and primers that were designed according to findings from our algorithm in this study.

摘要

虽然 SARS-CoV-2 的全基因组序列已经被揭示,但也表明 SARS-CoV-2 的基因组与 SARS-CoV 和 MERS-CoV 的基因组分别具有 80%和 50%的同源性。鉴于 SARS-CoV-2 的感染和死亡率数据,COVID-19 的诊断和治疗在全球范围内变得突出。因此,许多生物技术科学家已经开发出了 RT-PCR 试剂盒。然而,病毒是快速变异的生物体,为了提高准确性、长期可行性并避免 RT-PCR 检测的非特异性结果,具有低突变率的病毒基因组区域和针对这些区域的引物设计非常重要。在这方面,我们提出了一种新的算法,可用于寻找 SARS-CoV-2 的低突变率区域,并根据我们在这项研究中的算法发现设计引物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fab0/8015351/a195acd0ce50/gr7_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fab0/8015351/4c77b8dbd629/ga1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fab0/8015351/08317e736e1f/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fab0/8015351/c3e52b2509aa/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fab0/8015351/8ccc3ecbfed1/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fab0/8015351/927a909b5faa/gr4_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fab0/8015351/decc00c46a00/gr5_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fab0/8015351/b1fa8302917e/gr6_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fab0/8015351/a195acd0ce50/gr7_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fab0/8015351/4c77b8dbd629/ga1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fab0/8015351/08317e736e1f/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fab0/8015351/c3e52b2509aa/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fab0/8015351/8ccc3ecbfed1/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fab0/8015351/927a909b5faa/gr4_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fab0/8015351/decc00c46a00/gr5_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fab0/8015351/b1fa8302917e/gr6_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fab0/8015351/a195acd0ce50/gr7_lrg.jpg

相似文献

1
A novel method for conserved sequence extraction with prospective mutation prediction for SARS-CoV-2 PCR primer design.一种用于 SARS-CoV-2 PCR 引物设计的保守序列提取新方法,具有前瞻性突变预测。
J Virol Methods. 2021 Jul;293:114146. doi: 10.1016/j.jviromet.2021.114146. Epub 2021 Apr 1.
2
Identification of nsp1 gene as the target of SARS-CoV-2 real-time RT-PCR using nanopore whole-genome sequencing.利用纳米孔全基因组测序鉴定 SARS-CoV-2 实时 RT-PCR 的 nsp1 基因靶标。
J Med Virol. 2020 Nov;92(11):2725-2734. doi: 10.1002/jmv.26140. Epub 2020 Jun 19.
3
How to choose the right real-time RT-PCR primer sets for the SARS-CoV-2 genome detection?如何选择用于 SARS-CoV-2 基因组检测的合适实时 RT-PCR 引物?
J Virol Methods. 2021 Sep;295:114197. doi: 10.1016/j.jviromet.2021.114197. Epub 2021 May 24.
4
Design and in silico validation of polymerase chain reaction primers to detect severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2).设计并在计算机上验证聚合酶链反应引物以检测严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)。
Sci Rep. 2021 Jun 15;11(1):12565. doi: 10.1038/s41598-021-91817-9.
5
Deepening of In Silico Evaluation of SARS-CoV-2 Detection RT-qPCR Assays in the Context of New Variants.在新变种背景下对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)检测逆转录定量聚合酶链反应(RT-qPCR)检测方法进行深入的计算机模拟评估
Genes (Basel). 2021 Apr 13;12(4):565. doi: 10.3390/genes12040565.
6
Comparison of SARS-CoV-2 N gene real-time RT-PCR targets and commercially available mastermixes.比较 SARS-CoV-2 N 基因实时 RT-PCR 靶标和市售主混合物。
J Virol Methods. 2021 Sep;295:114215. doi: 10.1016/j.jviromet.2021.114215. Epub 2021 Jun 21.
7
Isothermal recombinase polymerase amplification-lateral flow detection of SARS-CoV-2, the etiological agent of COVID-19.恒温重组酶聚合酶扩增-侧向流动检测 SARS-CoV-2,COVID-19 的病原体。
J Virol Methods. 2021 Oct;296:114227. doi: 10.1016/j.jviromet.2021.114227. Epub 2021 Jul 2.
8
In-silico primer designing and PCR for detection of novel coronavirus-19.用于检测新型冠状病毒-19的电子引物设计与聚合酶链反应
J Infect Public Health. 2020 Dec;13(12):1885-1886. doi: 10.1016/j.jiph.2020.10.010. Epub 2020 Oct 23.
9
A simple method for detection of a novel coronavirus (SARS-CoV-2) using one-step RT-PCR followed by restriction fragment length polymorphism.一种使用一步 RT-PCR 结合限制性片段长度多态性检测新型冠状病毒(SARS-CoV-2)的简单方法。
J Med Virol. 2020 Nov;92(11):2839-2846. doi: 10.1002/jmv.26171. Epub 2020 Jun 29.
10
Comparative effects of viral-transport-medium heat inactivation upon downstream SARS-CoV-2 detection in patient samples.比较病毒运输介质热失活对患者样本中 SARS-CoV-2 后续检测的影响。
J Med Microbiol. 2021 Mar;70(3). doi: 10.1099/jmm.0.001301. Epub 2021 Mar 18.

引用本文的文献

1
Solid-state nanopore quantification of discrete sequence motifs from DNA and RNA targets in human plasma.人血浆中DNA和RNA靶标的离散序列基序的固态纳米孔定量分析。
Analyst. 2025 Jun 25. doi: 10.1039/d5an00373c.

本文引用的文献

1
Management and Treatment of COVID-19: The Chinese Experience.COVID-19 的管理和治疗:中国经验。
Can J Cardiol. 2020 Jun;36(6):915-930. doi: 10.1016/j.cjca.2020.04.010. Epub 2020 Apr 17.
2
Coding potential and sequence conservation of SARS-CoV-2 and related animal viruses.SARS-CoV-2 及相关动物病毒的编码潜力和序列保守性。
Infect Genet Evol. 2020 Sep;83:104353. doi: 10.1016/j.meegid.2020.104353. Epub 2020 May 5.
3
Analysis of therapeutic targets for SARS-CoV-2 and discovery of potential drugs by computational methods.
通过计算方法分析严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的治疗靶点并发现潜在药物
Acta Pharm Sin B. 2020 May;10(5):766-788. doi: 10.1016/j.apsb.2020.02.008. Epub 2020 Feb 27.
4
Structural and Functional Basis of SARS-CoV-2 Entry by Using Human ACE2.利用人血管紧张素转化酶 2 进入 SARS-CoV-2 的结构和功能基础
Cell. 2020 May 14;181(4):894-904.e9. doi: 10.1016/j.cell.2020.03.045. Epub 2020 Apr 9.
5
Coronavirus Disease 19 (COVID-19): Implications for Clinical Dental Care.新型冠状病毒病 19(COVID-19):对临床牙科护理的影响。
J Endod. 2020 May;46(5):584-595. doi: 10.1016/j.joen.2020.03.008. Epub 2020 Apr 6.
6
Genotype and phenotype of COVID-19: Their roles in pathogenesis.新型冠状病毒肺炎的基因型和表型:在发病机制中的作用。
J Microbiol Immunol Infect. 2021 Apr;54(2):159-163. doi: 10.1016/j.jmii.2020.03.022. Epub 2020 Mar 31.
7
COVID-19 infection: Origin, transmission, and characteristics of human coronaviruses.新型冠状病毒肺炎感染:人类冠状病毒的起源、传播及特征
J Adv Res. 2020 Mar 16;24:91-98. doi: 10.1016/j.jare.2020.03.005. eCollection 2020 Jul.
8
Neutralizing Antibodies against SARS-CoV-2 and Other Human Coronaviruses.针对 SARS-CoV-2 和其他人类冠状病毒的中和抗体。
Trends Immunol. 2020 May;41(5):355-359. doi: 10.1016/j.it.2020.03.007. Epub 2020 Apr 2.
9
Insight into 2019 novel coronavirus - An updated interim review and lessons from SARS-CoV and MERS-CoV.对 2019 年新型冠状病毒的洞察——来自 SARS-CoV 和 MERS-CoV 的更新中期综述和经验教训。
Int J Infect Dis. 2020 May;94:119-124. doi: 10.1016/j.ijid.2020.03.071. Epub 2020 Apr 1.
10
A Sequence Homology and Bioinformatic Approach Can Predict Candidate Targets for Immune Responses to SARS-CoV-2.一种序列同源性和生物信息学方法可预测针对 SARS-CoV-2 的免疫反应的候选靶点。
Cell Host Microbe. 2020 Apr 8;27(4):671-680.e2. doi: 10.1016/j.chom.2020.03.002. Epub 2020 Mar 16.