用于基因表达谱分析的高通量qPCR的自动化和小型化。

IF 2.5 4区 医学 Q3 BIOCHEMICAL RESEARCH METHODS SLAS Technology Pub Date : 2024-12-25 DOI:10.1016/j.slast.2024.100241
Santhi Raveendran, Asma Saeed, Mahesh Kumar Reddy Kalikiri, Harshitha Shobha Manjunath, Alia Al Massih, Muna Al Hashmi, Iman Al Azwani, Basirudeen Syed Ahamed Kabeer, Rebecca Mathew, Sara Tomei
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引用次数: 0

摘要

定量PCR (qPCR)是实验室和核心设施中常用的一种技术。在我们之前的研究中,我们已经展示了通过将蚊子HV与BioMark HD配对来自动化面板特异性基因表达工作流程步骤的可能性。在这里,我们的目标是自动化整个工作流并探索小型化功能。基因表达流程的每一步都在Mosquito HV基因组软件上编写脚本。我们进行了三种不同的自动化运行:i.在免疫学基因表达面板上运行参考RNA样本(通过汇集从10个健康个体分离的RNA获得)的复制。我们测试了全反应(FR)和3种小型化条件,即1.5倍、2.5倍和5倍;将自动FR重复获得的数据与手工处理获得的数据进行比较;2。生物RNA样本(从n=45个个体中分离)在免疫学基因表达面板上作为FR和1.5倍运行;3。生物RNA样本(从n=45个个体中分离)在妊娠基因表达面板上作为FR和1.5倍运行。采用2(- δ δ Ct)法计算各基因的表达量。在FR和1.5倍条件下,观察到参考样品扩增成功。2.5倍条件下扩增效果不佳,成功率较低,而5倍条件下没有扩增。2.5倍和5倍的小型化条件被排除在进一步的运行中。在参考RNA样本的手动和自动化工作流程之间观察到强烈的显著正相关,强调了基因表达测定的稳健性。在FR和1.5倍小型化条件下,45个个体样本的免疫学和妊娠基因表达面板的自动化成功率均为70%。在两个面板的FR和1.5倍小型化条件之间也观察到显著的正相关。我们的研究结果表明,采用蚊子HV系统自动化基因表达工作流程和1.5倍的小型化能力不会影响数据质量和可重复性。
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Automation and miniaturization of high-throughput qPCR for gene expression profiling.

Quantitative PCR (qPCR) is a technique commonly employed in laboratories and core facilities. In our previous study, we had shown the possibility to automate steps in a panel-specific gene expression workflow by pairing Mosquito HV with BioMark HD. Here we aimed to automate the full workflow and explore miniaturization capabilities. Each step of the gene expression workflow was scripted on Mosquito HV genomics software. We performed three different automated runs: i. Replicates of a Reference RNA sample (obtained by pooling RNA isolated from 10 healthy individuals) were run on an immunology gene expression panel. We tested the full reaction (FR) and three miniaturization conditions, namely: 1.5x, 2.5x and 5x; the data obtained from the automated FR replicates was compared to the data obtained from the manual processing; ii. Biological RNA samples (isolated from n = 45 individuals) were run as FR and 1.5x on the immunology gene expression panel; iii. Biological RNA samples (isolated from n = 45 individuals) were run as FR and 1.5x on a pregnancy gene expression panel. The expression of each gene was calculated using the 2(-delta Ct) method. Successful amplification was observed for the reference samples when using FR and 1.5x conditions. The 2.5x condition exhibited suboptimal amplification with a lower success rate while the 5x condition retrieved no amplification. The 2.5x and 5x miniaturization conditions were excluded from further runs. A strong significant positive correlation was observed between the manual and automated workflows for the reference RNA sample, underscoring the robustness of the gene expression assay. The automation of the immunology and pregnancy gene expression panels on the 45 individual samples retrieved a success rate >70 % for both the FR and the 1.5x miniaturization conditions. A significant positive correlation was also observed between the FR and 1.5x miniaturization conditions for both panels. Our results show that the adoption and the 1.5x miniaturization capabilities of Mosquito HV system for automating the gene expression workflow did not interfere with data quality and reproducibility.

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来源期刊
SLAS Technology
SLAS Technology Computer Science-Computer Science Applications
CiteScore
6.30
自引率
7.40%
发文量
47
审稿时长
106 days
期刊介绍: SLAS Technology emphasizes scientific and technical advances that enable and improve life sciences research and development; drug-delivery; diagnostics; biomedical and molecular imaging; and personalized and precision medicine. This includes high-throughput and other laboratory automation technologies; micro/nanotechnologies; analytical, separation and quantitative techniques; synthetic chemistry and biology; informatics (data analysis, statistics, bio, genomic and chemoinformatics); and more.
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