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利用 PCR.Ai 实现定量多重 PCR 检测的自动化和标准化

Automation and standardisation of a quantitative multiplex PCR assay using PCR.Ai.

机构信息

West of Scotland Specialist Virology Centre, New Lister Building, Glasgow Royal Infirmary, 10-16 Alexandra Parade, Glasgow G31 2ER, United Kingdom.

West of Scotland Specialist Virology Centre, New Lister Building, Glasgow Royal Infirmary, 10-16 Alexandra Parade, Glasgow G31 2ER, United Kingdom.

出版信息

J Virol Methods. 2024 Sep;329:114981. doi: 10.1016/j.jviromet.2024.114981. Epub 2024 Jul 14.

Abstract

BACKGROUND

We previously undertook a prospective clinical study to evaluate PCR.Ai's (www.pcr.ai) accuracy and impact when automating the manual data-analysis and quality control steps associated with routine clinical pathogen testing using a non-quantitative multiplex quantitative real-time PCR (qPCR). In this study we demonstrated 100 % concurrence between our manual routine analysis method and PCR.Ai. This paper expands the evaluation of PCR.Ai's (www.pcr.ai) accuracy and impact using a multiplex quantitative real-time PCR (qPCR).

OBJECTIVES

We evaluated the impact of PCR.Ai when used as the final interpretation/verification step for routine in-house multiplex quantitative qPCR tests for CMV, EBV and adenovirus from blood samples for a total of 1350 interpretations.

STUDY DESIGN

We compared PCR.Ai to our existing manual interpretation, to determine accuracy and hands on time savings.

RESULTS AND CONCLUSIONS

There was 100 % concurrence between validated CMV, EBV and adenovirus detection and quantitation by our manual routine analysis method and PCR.Ai. Furthermore, there were significant routine savings with PCR.Ai of 63 minutes/ run. Our conclusion is that for quantitative tests PCR.Ai is a highly accurate time-saving tool that reduces complexity of qPCR analysis and hence the need for specialists and hands-on time. It demonstrated capabilities to enable us to get results out more quickly with lower costs and less risk of errors.

摘要

背景

我们之前进行了一项前瞻性临床研究,以评估 PCR.Ai(www.pcr.ai)在自动化与常规临床病原体检测相关的手动数据分析和质量控制步骤时的准确性和影响,该检测使用非定量多重实时定量 PCR(qPCR)。在这项研究中,我们证明了我们的手动常规分析方法与 PCR.Ai 之间的 100%一致性。本文扩展了对 PCR.Ai(www.pcr.ai)准确性和影响的评估,使用了多重实时定量 PCR(qPCR)。

目的

我们评估了在总共 1350 次解释中,将 PCR.Ai 用作常规内部多重实时 qPCR 测试(用于血液样本中的 CMV、EBV 和腺病毒)的最终解释/验证步骤时的影响。

研究设计

我们将 PCR.Ai 与我们现有的手动解释进行了比较,以确定准确性和节省人工时间。

结果与结论

我们的手动常规分析方法和 PCR.Ai 对 CMV、EBV 和腺病毒的检测和定量完全一致。此外,使用 PCR.Ai 可以节省 63 分钟/运行的常规工作时间。我们的结论是,对于定量测试,PCR.Ai 是一种高度准确且节省时间的工具,可以减少 qPCR 分析的复杂性,从而减少对专家和人工时间的需求。它展示了使我们能够更快地获得结果、降低成本和减少错误风险的能力。

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