College of Science and Engineering, Flinders University, GPO Box 2100, Adelaide, SA 5001, Australia.
Forensic Science SA, GPO Box 2790, Adelaide, SA 5001, Australia.
Genes (Basel). 2024 Sep 12;15(9):1199. doi: 10.3390/genes15091199.
The introduction of PCR into forensic science and the rapid increases in the sensitivity, specificity and discrimination power of DNA profiling that followed have been fundamental in shaping the field of forensic biology. Despite these developments, the challenges associated with the DNA profiling of trace, inhibited and degraded samples remain. Thus, any improvement to the performance of sub-optimal samples in DNA profiling would be of great value to the forensic community. The potential exists to optimise the PCR performance of samples by altering the cycling conditions used. If the effects of changing cycling conditions upon the quality of a DNA profile can be well understood, then the PCR process can be manipulated to achieve a specific goal. This work is a proof-of-concept study for the development of a smart PCR system, the theoretical foundations of which are outlined in part 1 of this publication. The first steps needed to demonstrate the performance of our smart PCR goal involved the manual alteration of cycling conditions and assessment of the DNA profiles produced. In this study, the timing and temperature of the denaturation and annealing stages of the PCR were manually altered to achieve the goal of reducing PCR runtime while maintaining an acceptable quality and quantity of DNA product. A real-time feedback system was also trialled using an STR PCR and qPCR reaction mix, and the DNA profiles generated were compared to profiles produced using the standard STR PCR kits. The aim of this work was to leverage machine learning to enable real-time adjustments during a PCR, allowing optimisation of cycling conditions towards predefined user goals. A set of parameters was found that yielded similar results to the standard endpoint PCR methodology but was completed 30 min faster. The development of an intelligent system would have significant implications for the various biological disciplines that are reliant on PCR technology.
PCR 技术引入法庭科学以及随后 DNA 图谱分析的灵敏度、特异性和辨别能力的快速提高,是法庭生物学领域发展的基础。尽管有了这些发展,痕量、抑制和降解样本的 DNA 图谱分析仍然存在挑战。因此,任何提高 DNA 图谱分析中次优样本性能的方法都将对法庭科学界具有重要价值。通过改变使用的循环条件,可以优化样本的 PCR 性能。如果能够很好地理解改变循环条件对 DNA 图谱质量的影响,那么就可以操纵 PCR 过程以达到特定目标。这项工作是开发智能 PCR 系统的概念验证研究,其理论基础在本出版物的第 1 部分中概述。为了展示我们的智能 PCR 目标的性能,首先需要手动改变循环条件并评估产生的 DNA 图谱。在这项研究中,手动改变了 PCR 的变性和退火阶段的时间和温度,以达到在保持可接受的 DNA 产物质量和数量的同时减少 PCR 运行时间的目标。还使用实时反馈系统对 STR PCR 和 qPCR 反应混合物进行了试验,并将生成的 DNA 图谱与使用标准 STR PCR 试剂盒生成的图谱进行了比较。这项工作的目的是利用机器学习在 PCR 过程中进行实时调整,从而优化循环条件以满足预定义的用户目标。找到了一组参数,其结果与标准终点 PCR 方法相似,但完成时间快了 30 分钟。智能系统的开发将对依赖 PCR 技术的各种生物学学科产生重大影响。