• 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

quantGenius:基于定量聚合酶链反应的基因定量决策支持系统的实现

quantGenius: implementation of a decision support system for qPCR-based gene quantification.

作者信息

Baebler Špela, Svalina Miha, Petek Marko, Stare Katja, Rotter Ana, Pompe-Novak Maruša, Gruden Kristina

机构信息

Department of Biotechnology and Systems Biology, National Institute of Biology, Ljubljana, 1000, SI, Slovenia.

出版信息

BMC Bioinformatics. 2017 May 25;18(1):276. doi: 10.1186/s12859-017-1688-7.

DOI:10.1186/s12859-017-1688-7
PMID:28545393
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5445471/
Abstract

BACKGROUND

Quantitative molecular biology remains a challenge for researchers due to inconsistent approaches for control of errors in the final results. Due to several factors that can influence the final result, quantitative analysis and interpretation of qPCR data are still not trivial. Together with the development of high-throughput qPCR platforms, there is a need for a tool allowing for robust, reliable and fast nucleic acid quantification.

RESULTS

We have developed "quantGenius" ( http://quantgenius.nib.si ), an open-access web application for a reliable qPCR-based quantification of nucleic acids. The quantGenius workflow interactively guides the user through data import, quality control (QC) and calculation steps. The input is machine- and chemistry-independent. Quantification is performed using the standard curve approach, with normalization to one or several reference genes. The special feature of the application is the implementation of user-guided QC-based decision support system, based on qPCR standards, that takes into account pipetting errors, assay amplification efficiencies, limits of detection and quantification of the assays as well as the control of PCR inhibition in individual samples. The intermediate calculations and final results are exportable in a data matrix suitable for further statistical analysis or visualization. We additionally compare the most important features of quantGenius with similar advanced software tools and illustrate the importance of proper QC system in the analysis of qPCR data in two use cases.

CONCLUSIONS

To our knowledge, quantGenius is the only qPCR data analysis tool that integrates QC-based decision support and will help scientists to obtain reliable results which are the basis for biologically meaningful data interpretation.

摘要

背景

由于在控制最终结果误差方面方法不一致,定量分子生物学对研究人员来说仍然是一项挑战。由于有几个因素会影响最终结果,qPCR数据的定量分析和解读仍然并非易事。随着高通量qPCR平台的发展,需要一种能够实现强大、可靠且快速的核酸定量的工具。

结果

我们开发了“quantGenius”(http://quantgenius.nib.si),这是一个基于qPCR的可靠核酸定量的开放获取网络应用程序。quantGenius工作流程以交互方式引导用户完成数据导入、质量控制(QC)和计算步骤。输入与仪器和化学方法无关。使用标准曲线法进行定量,并以一个或几个参考基因进行归一化。该应用程序的特殊之处在于基于qPCR标准实现了用户引导的基于QC的决策支持系统,该系统考虑了移液误差、检测方法的扩增效率、检测限和定量限以及单个样品中PCR抑制的控制。中间计算结果和最终结果可以导出为适合进一步统计分析或可视化的数据矩阵。我们还将quantGenius的最重要特征与类似的先进软件工具进行了比较,并在两个应用案例中说明了适当的QC系统在qPCR数据分析中的重要性。

结论

据我们所知,quantGenius是唯一集成了基于QC的决策支持的qPCR数据分析工具,将帮助科学家获得可靠的结果,这些结果是进行生物学意义数据解读的基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dba/5445471/b2f340658a46/12859_2017_1688_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dba/5445471/8c7dc4e44745/12859_2017_1688_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dba/5445471/e29c7fae4a6a/12859_2017_1688_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dba/5445471/1c26b6e602dd/12859_2017_1688_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dba/5445471/19ab5d2ec047/12859_2017_1688_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dba/5445471/b2f340658a46/12859_2017_1688_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dba/5445471/8c7dc4e44745/12859_2017_1688_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dba/5445471/e29c7fae4a6a/12859_2017_1688_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dba/5445471/1c26b6e602dd/12859_2017_1688_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dba/5445471/19ab5d2ec047/12859_2017_1688_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dba/5445471/b2f340658a46/12859_2017_1688_Fig5_HTML.jpg

相似文献

1
quantGenius: implementation of a decision support system for qPCR-based gene quantification.quantGenius:基于定量聚合酶链反应的基因定量决策支持系统的实现
BMC Bioinformatics. 2017 May 25;18(1):276. doi: 10.1186/s12859-017-1688-7.
2
Web-based LinRegPCR: application for the visualization and analysis of (RT)-qPCR amplification and melting data.基于网络的 LinRegPCR:用于可视化和分析(RT)-qPCR 扩增和熔解数据的应用程序。
BMC Bioinformatics. 2021 Aug 24;22(1):398. doi: 10.1186/s12859-021-04306-1.
3
Fluorescent amplification for next generation sequencing (FA-NGS) library preparation.荧光扩增下一代测序(FA-NGS)文库制备。
BMC Genomics. 2020 Jan 28;21(1):85. doi: 10.1186/s12864-020-6481-8.
4
The dilution effect and the importance of selecting the right internal control genes for RT-qPCR: a paradigmatic approach in fetal sheep.稀释效应以及为逆转录定量聚合酶链反应选择合适内参基因的重要性:绵羊胎儿中的一种典型方法
BMC Res Notes. 2015 Feb 27;8:58. doi: 10.1186/s13104-015-0973-7.
5
Chainy: an universal tool for standardized relative quantification in real-time PCR.Chainy:一种用于实时PCR标准化相对定量的通用工具。
Bioinformatics. 2017 May 1;33(9):1411-1413. doi: 10.1093/bioinformatics/btw839.
6
QPCR: Application for real-time PCR data management and analysis.QPCR:实时 PCR 数据管理与分析应用。
BMC Bioinformatics. 2009 Aug 27;10:268. doi: 10.1186/1471-2105-10-268.
7
New approaches for the standardization and validation of a real-time qPCR assay using TaqMan probes for quantification of yellow fever virus on clinical samples with high quality parameters.使用TaqMan探针进行实时定量PCR检测以对具有高质量参数的临床样本中的黄热病毒进行定量分析的标准化和验证的新方法。
Hum Vaccin Immunother. 2015;11(7):1865-71. doi: 10.4161/21645515.2014.990854.
8
QuantPrime--a flexible tool for reliable high-throughput primer design for quantitative PCR.QuantPrime——一种用于定量PCR可靠高通量引物设计的灵活工具。
BMC Bioinformatics. 2008 Nov 1;9:465. doi: 10.1186/1471-2105-9-465.
9
Direct qPCR quantification of unprocessed forensic casework samples.未经处理的法医案件样本的直接定量聚合酶链反应(qPCR)分析
Forensic Sci Int Genet. 2014 Jul;11:96-104. doi: 10.1016/j.fsigen.2014.03.003. Epub 2014 Mar 15.
10
Development and evaluation of a novel RT-qPCR based test for the quantification of HER2 gene expression in breast cancer.一种基于实时定量聚合酶链反应(RT-qPCR)的新型检测方法用于乳腺癌中HER2基因表达定量的开发与评估。
Gene. 2017 Mar 20;605:114-122. doi: 10.1016/j.gene.2016.12.027. Epub 2016 Dec 28.

引用本文的文献

1
Integration of multi-omics data and deep phenotyping provides insights into responses to single and combined abiotic stress in potato.多组学数据与深度表型分析的整合为洞察马铃薯对单一和复合非生物胁迫的响应提供了见解。
Plant Physiol. 2025 Mar 28;197(4). doi: 10.1093/plphys/kiaf126.
2
The Slovenian translational platform GlioBank for brain tumor research: Identification of molecular signatures of glioblastoma progression.用于脑肿瘤研究的斯洛文尼亚翻译平台Gliobank:胶质母细胞瘤进展分子特征的鉴定。
Neurooncol Adv. 2025 Jan 22;7(1):vdaf015. doi: 10.1093/noajnl/vdaf015. eCollection 2025 Jan-Dec.
3
Chloroplast Vesiculation and Induced and Expression During Tomato Flower Pedicel Abscission.

本文引用的文献

1
A survey of tools for the analysis of quantitative PCR (qPCR) data.定量聚合酶链反应(qPCR)数据分析工具综述。
Biomol Detect Quantif. 2014 Sep 6;1(1):23-33. doi: 10.1016/j.bdq.2014.08.002. eCollection 2014 Sep.
2
How good is a PCR efficiency estimate: Recommendations for precise and robust qPCR efficiency assessments.PCR效率估计的准确性如何:精确且稳健的qPCR效率评估建议
Biomol Detect Quantif. 2015 Mar 11;3:9-16. doi: 10.1016/j.bdq.2015.01.005. eCollection 2015 Mar.
3
The FAIR Guiding Principles for scientific data management and stewardship.
叶绿体囊泡化与番茄花柄脱落过程中的诱导及表达
Plant Direct. 2025 Jan 8;9(1):e70035. doi: 10.1002/pld3.70035. eCollection 2025 Jan.
4
Patient-derived tumor organoids mimic treatment-induced DNA damage response in glioblastoma.患者来源的肿瘤类器官模拟胶质母细胞瘤中治疗诱导的DNA损伤反应。
iScience. 2024 Jul 31;27(9):110604. doi: 10.1016/j.isci.2024.110604. eCollection 2024 Sep 20.
5
Stress Knowledge Map: A knowledge graph resource for systems biology analysis of plant stress responses.应激知识图谱:用于植物应激反应系统生物学分析的知识图谱资源。
Plant Commun. 2024 Jun 10;5(6):100920. doi: 10.1016/j.xplc.2024.100920. Epub 2024 Apr 15.
6
Anti-Vimentin Nanobody Decreases Glioblastoma Cell Invasion In Vitro and In Vivo.抗波形蛋白纳米抗体在体外和体内均可降低胶质母细胞瘤细胞的侵袭能力。
Cancers (Basel). 2023 Jan 17;15(3):573. doi: 10.3390/cancers15030573.
7
A mini-TGA protein modulates gene expression through heterogeneous association with transcription factors.一种微型 TGA 蛋白通过与转录因子的异质结合来调节基因表达。
Plant Physiol. 2023 Mar 17;191(3):1934-1952. doi: 10.1093/plphys/kiac579.
8
CRISPR/Cas9-mediated fine-tuning of miRNA expression in tetraploid potato.CRISPR/Cas9介导的四倍体马铃薯中微小RNA表达的微调
Hortic Res. 2022 Jun 30;9:uhac147. doi: 10.1093/hr/uhac147. eCollection 2022.
9
Chloroplast redox state changes mark cell-to-cell signaling in the hypersensitive response.叶绿体氧化还原状态变化标志着细胞间信号在超敏反应中的传递。
New Phytol. 2023 Jan;237(2):548-562. doi: 10.1111/nph.18425. Epub 2022 Sep 1.
10
Physiological and Transcriptional Responses to Saline Irrigation of Young 'Tempranillo' Vines Grafted Onto Different Rootstocks.嫁接到不同砧木上的幼龄“丹魄”葡萄藤对盐水灌溉的生理和转录反应
Front Plant Sci. 2022 Jun 6;13:866053. doi: 10.3389/fpls.2022.866053. eCollection 2022.
科学数据管理和保存的 FAIR 指导原则。
Sci Data. 2016 Mar 15;3:160018. doi: 10.1038/sdata.2016.18.
4
Tools and data services registry: a community effort to document bioinformatics resources.工具与数据服务注册库:记录生物信息学资源的社区协作项目。
Nucleic Acids Res. 2016 Jan 4;44(D1):D38-47. doi: 10.1093/nar/gkv1116. Epub 2015 Nov 3.
5
Robust regression methods for real-time polymerase chain reaction.实时聚合酶链反应的稳健回归方法
Anal Biochem. 2015 Jul 1;480:34-6. doi: 10.1016/j.ab.2015.04.001. Epub 2015 Apr 8.
6
limma powers differential expression analyses for RNA-sequencing and microarray studies.limma为RNA测序和微阵列研究提供差异表达分析的动力。
Nucleic Acids Res. 2015 Apr 20;43(7):e47. doi: 10.1093/nar/gkv007. Epub 2015 Jan 20.
7
Reliable gene expression analysis by reverse transcription-quantitative PCR: reporting and minimizing the uncertainty in data accuracy.通过逆转录定量PCR进行可靠的基因表达分析:报告并最小化数据准确性的不确定性
Plant Cell. 2014 Oct;26(10):3829-37. doi: 10.1105/tpc.114.130641. Epub 2014 Oct 31.
8
Variability of the reverse transcription step: practical implications.反转录步骤的变异性:实际意义。
Clin Chem. 2015 Jan;61(1):202-12. doi: 10.1373/clinchem.2014.230615. Epub 2014 Oct 31.
9
On non-detects in qPCR data.关于qPCR数据中的未检测到情况。
Bioinformatics. 2014 Aug 15;30(16):2310-6. doi: 10.1093/bioinformatics/btu239. Epub 2014 Apr 23.
10
Salicylic acid is an indispensable component of the Ny-1 resistance-gene-mediated response against Potato virus Y infection in potato.水杨酸是马铃薯中Ny-1抗性基因介导的抗马铃薯Y病毒感染反应中不可或缺的组成部分。
J Exp Bot. 2014 Mar;65(4):1095-109. doi: 10.1093/jxb/ert447. Epub 2014 Jan 13.