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开发用于大规模并行测序的多重法医身份鉴定面板及其使用实验设计的系统优化。

Development of a multiplex forensic identity panel for massively parallel sequencing and its systematic optimization using design of experiments.

机构信息

LABCON-OWL Analytik, Forschung und Consulting GmbH, Siemensstr. 40, 32105 Bad Salzuflen, Germany.

LABCON-OWL Analytik, Forschung und Consulting GmbH, Siemensstr. 40, 32105 Bad Salzuflen, Germany.

出版信息

Forensic Sci Int Genet. 2019 Mar;39:32-43. doi: 10.1016/j.fsigen.2018.11.023. Epub 2018 Nov 30.

Abstract

The application of massively parallel sequencing (MPS) in forensic sciences enables high-resolution short tandem repeat (STR) genotyping for the characterization of biological evidence. While MPS supports multiplexing of a large number of forensic markers, the performance of an MPS-STR panel depends on good primer design and optimal PCR conditions. However, conventional strategies for multifactorial assay optimization are labor-intensive and do not necessarily allow the experimenter to identify optimum factor settings. Here we describe our new multiplex PCR assay, monSTR, which supports the simultaneous amplification of 21 forensic markers followed by targeted sequencing on the Illumina MiSeq. The selection of STR markers adapts on the expanded European Standard Set (ESS), including the highly polymorphic locus SE33, for compatibility with existing forensic DNA databases. Primer engineering involved bioinformatics tools to create a multiplex-compatible primer set. Primer quality was evaluated in silico and in vitro. We demonstrate the systematic optimization of multiplex PCR thermocycling conditions using Design of Experiments (DOE) methodology. The objective was to yield a specific, balanced, low-noise amplification of forensic targets. A central composite face design of experiments enabled an efficient simultaneous investigation of multiple critical process parameters and their interactions. Optimal multiplex PCR conditions were predicted using software-aided modelling based on DOE data. Verification experiments suggested a balanced, reproducible amplification of all markers with reduced formation of artefacts. Fully concordant STR profiles were obtained for the investigated reference samples even with challenging input DNA concentrations. We found that application of DOE principles enabled an experimentally practical and economically justifiable assay development and optimization, even beyond the field of forensic genetics.

摘要

高通量测序(MPS)在法医学中的应用使我们能够对生物证据进行高分辨率短串联重复序列(STR)基因分型。虽然 MPS 支持大量法医标记物的多重检测,但 MPS-STR 面板的性能取决于良好的引物设计和最佳的 PCR 条件。然而,传统的多因素分析优化策略既繁琐又不能确保实验人员确定最佳的因子设置。在这里,我们描述了一种新的多重 PCR 检测方法 monSTR,它支持同时扩增 21 个法医标记物,然后在 Illumina MiSeq 上进行靶向测序。STR 标记的选择适用于扩展的欧洲标准集(ESS),包括高度多态性的 SE33 位点,以与现有的法医 DNA 数据库兼容。引物设计涉及生物信息学工具来创建一个多重兼容的引物集。我们通过计算机模拟和体外实验评估了引物质量。我们使用实验设计(DoE)方法来系统地优化多重 PCR 热循环条件。目标是获得特定、平衡、低噪声的法医靶标扩增。中心复合面设计的实验可以有效地同时研究多个关键过程参数及其相互作用。最优的多重 PCR 条件是基于 DOE 数据的软件辅助建模预测的。验证实验表明,所有标记的扩增都具有平衡、可重复的特点,并且减少了伪影的形成。即使在具有挑战性的输入 DNA 浓度下,对研究用参考样本也能获得完全一致的 STR 谱。我们发现,即使在法医遗传学领域之外,DoE 原理的应用也能实现具有实际实验可行性和经济合理性的检测方法的开发和优化。

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