Senst Alina, Bonsiepe Hannah, Kron Sarah, Schulz Iris
Institute of Forensic Medicine, University Basel, Basel, Switzerland.
J Forensic Sci. 2024 Nov;69(6):2192-2196. doi: 10.1111/1556-4029.15601. Epub 2024 Aug 21.
Next-generation sequencing (NGS) technologies have expanded the spectrum of forensic DNA analysis by facilitating efficient and precise genotyping of a large number of genetic markers. Yet, challenges persist regarding complex sample processing and assurance of equal molar concentrations across pooled samples. Since optimal cluster density is crucial for sequencing performance, the determination of both quantity and quality is indispensable for library preparation. In this study, we investigated the application of the Agilent 2100 Bioanalyzer for library quality control, as studies for forensic approaches, particularly for highly degraded postmortem samples, are rare. Our analysis encompassed assessing total DNA concentrations, fluorescence unit (FU) values, and adapter dimer concentrations in purified DNA libraries derived from buccal swabs and tissue samples of decomposed corpses. The sensitivity study tested a serial dilution derived from buccal swabs and revealed a decrease in FU values and an increase in adapter dimers with declining DNA input concentrations. Deviations in total DNA concentrations and average peak heights between the Agilent 2100 Bioanalyzer runs indicated a lack of repeatability in data and presented challenges in accurate quantification, which was also observed in previous studies. Yet, the analysis of degraded samples from decomposed human remains has shown the ability to detect adapter dimer concentrations, which can be crucial for the quality of subsequent NGS library preparation and sequencing success. Therefore, the Agilent 2100 Bioanalyzer proves to be a valuable tool for NGS quality control.
下一代测序(NGS)技术通过促进对大量遗传标记进行高效、精确的基因分型,扩大了法医DNA分析的范围。然而,在复杂样本处理以及确保混合样本中具有相等摩尔浓度方面,挑战依然存在。由于最佳簇密度对测序性能至关重要,因此在文库制备过程中,确定DNA的数量和质量都是必不可少的。在本研究中,我们调查了安捷伦2100生物分析仪在文库质量控制中的应用,因为针对法医应用,特别是针对高度降解的死后样本的研究很少。我们的分析包括评估来自口腔拭子和腐烂尸体组织样本的纯化DNA文库中的总DNA浓度、荧光单位(FU)值和接头二聚体浓度。敏感性研究测试了一系列来自口腔拭子的稀释样本,结果显示随着DNA输入浓度的降低,FU值下降,接头二聚体增加。安捷伦2100生物分析仪各次运行之间的总DNA浓度和平均峰高存在偏差,表明数据缺乏可重复性,在准确定量方面存在挑战,这在以前的研究中也有观察到。然而,对来自腐烂人类遗骸的降解样本的分析表明,该方法能够检测接头二聚体浓度,这对于后续NGS文库制备的质量和测序成功至关重要。因此,安捷伦2100生物分析仪被证明是用于NGS质量控制的一种有价值的工具。