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使用扩增子RX PCR后净化试剂盒提高法医案件工作中微量DNA图谱的回收率。

Enhancing trace DNA profile recovery in forensic casework using the amplicon RX post-PCR clean-up kit.

作者信息

Aljanahi Naeema S, Alketbi Salem K, Almheiri Maryam M, Alshehhi Suaad A, Sanqoor Afra N, Alghanim Hussein J

机构信息

The Biology and DNA Section, General Department of Forensic Science and Criminology, Dubai Police General Head Quarters, Dubai, United Arab Emirates.

出版信息

Sci Rep. 2025 Jan 27;15(1):3324. doi: 10.1038/s41598-025-88164-4.

Abstract

This study evaluated the effectiveness of the amplicon RX post-PCR clean-up kit in enhancing trace DNA profile recovery from forensic casework samples amplified using the GlobalFiler PCR amplification kit. The impact of post-PCR clean-up on allele recovery and signal intensity was assessed in both trace casework samples and control samples across a range of DNA concentrations. The results showed that the amplicon RX method significantly improved allele recovery compared to the 29-cycle protocol (p = 8.30 × 10) and achieved slightly better results than the 30-cycle protocol (p = 0.019). Additionally, the Amplicon RX method demonstrated a significant increase in signal intensity (p = 2.70 × 10), reflecting improved sensitivity in detecting trace DNA profiles compared to the 30-cycle protocol. In the evaluation of control samples, the amplicon RX method consistently outperformed both the 29- and 30-cycle protocols, especially at lower DNA concentrations (D3: 0.001 ng/µL). While the performance of all methods declined at the lowest concentration (D4: 0.0001 ng/µL), the Amplicon RX method still demonstrated superior allele recovery (p = 0.014 compared to 29 cycles; p = 0.011 compared to 30 cycles). Therefore, the Amplicon RX method should be widely adopted in forensic laboratories to enhance the analysis of extremely low-template and compromised samples. These findings highlight the potential of the amplicon RX post-PCR clean-up kit to improve trace DNA analysis in forensic casework. Further research is recommended to validate these results and explore its broader application in forensic DNA analysis, particularly in complex DNA mixtures and extremely low-template samples.

摘要

本研究评估了扩增子RX PCR后净化试剂盒在增强使用GlobalFiler PCR扩增试剂盒扩增的法医案件样本中微量DNA图谱回收方面的有效性。在一系列DNA浓度的微量案件样本和对照样本中,评估了PCR后净化对等位基因回收和信号强度的影响。结果表明,与29个循环的方案相比,扩增子RX方法显著提高了等位基因回收率(p = 8.30×10),并且比30个循环的方案取得了稍好的结果(p = 0.019)。此外,扩增子RX方法显示信号强度显著增加(p = 2.70×10),这反映出与30个循环的方案相比,在检测微量DNA图谱方面灵敏度有所提高。在对照样本的评估中,扩增子RX方法始终优于29个循环和30个循环的方案,尤其是在较低DNA浓度(D3:0.001 ng/µL)时。虽然所有方法在最低浓度(D4:0.0001 ng/µL)下性能均下降,但扩增子RX方法仍显示出优异的等位基因回收率(与29个循环相比,p = 0.014;与30个循环相比,p = 0.011)。因此,扩增子RX方法应在法医实验室中广泛采用,以加强对极低模板量和受损样本的分析。这些发现突出了扩增子RX PCR后净化试剂盒在改善法医案件微量DNA分析方面的潜力。建议进一步开展研究以验证这些结果,并探索其在法医DNA分析中的更广泛应用,特别是在复杂DNA混合物和极低模板量样本中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a01/11770088/521212245bb7/41598_2025_88164_Fig1_HTML.jpg

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