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SeqStudioTM 遗传分析仪与 MiSeqTM FGx 法医基因组学系统在 Y-STR 分型中的一致性研究。

Concordance study on Y-STRs typing between SeqStudio™ genetic analyzer for HID and MiSeq™ FGx forensic genomics system.

机构信息

Department of Diagnostics and Public Health, Section of Forensic Medicine, Forensic Genetics Lab, University of Verona, Verona, Italy.

GM Lab, Department of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Verona, Italy.

出版信息

Mol Biol Rep. 2023 Dec;50(12):9779-9789. doi: 10.1007/s11033-023-08808-4. Epub 2023 Oct 9.

Abstract

BACKGROUND

Massively Parallel Sequencing (MPS) allowed an increased number of information to be retrieved from short tandem repeat (STR) analysis, expanding them not only to the size, as already performed in Capillary Electrophoresis (CE), but also to the sequence. MPS requires constant development and validation of the analytical parameters to ensure that the genotyping results of STRs correspond to those obtained by CE. Given the increased frequency of usage of Y-STRs as supplementary markers to the autosomal STRs analysis, it is urgent to validate the concordance of the typing results between CE and MPS analyses.

METHODS AND RESULTS

DNA extracted from 125 saliva samples of unrelated males was genotyped using Yfiler™ Plus PCR Amplification Kit and ForenSeq™ DNA Signature Prep Kit, which were analyzed by SeqStudio™ Genetic Analyzer for HID and MiSeq™ FGx Forensic Genomics System, respectively. For each shared Y-STR, allele designation, number of length- and sequence-based alleles per locus, stutter percentage, and the intra-locus balance of multicopy Y-STRs were screened.

CONCLUSIONS

Although the number of forensic genetics laboratories that are applying the MPS technique in routine analysis is small and does not allow a global assessment of MPS limitations, this comparative study highlights the ability of MPS to produce reliable profiles despite the generation of large amounts of raw data.

摘要

背景

高通量测序(MPS)允许从短串联重复序列(STR)分析中获取更多信息,不仅可以像毛细管电泳(CE)那样扩展 STR 的大小,还可以扩展到序列。MPS 需要不断开发和验证分析参数,以确保 STR 基因分型结果与 CE 获得的结果一致。鉴于 Y-STR 作为常染色体 STR 分析的补充标记的使用频率越来越高,迫切需要验证 CE 和 MPS 分析之间的分型结果的一致性。

方法和结果

使用 Yfiler ™ Plus PCR 扩增试剂盒和 ForenSeq ™ DNA 签名制备试剂盒对 125 名无关男性的唾液样本进行 DNA 分型,分别使用 SeqStudio ™ 遗传分析仪和 MiSeq ™ FGx 法医基因组系统进行 HID 和 MiSeq ™ FGx 法医基因组系统进行分析。筛选每个共享的 Y-STR 的等位基因指定、每个基因座的长度和基于序列的等位基因数量、等位基因突跳百分比以及多拷贝 Y-STR 的基因座内平衡。

结论

尽管应用 MPS 技术进行常规分析的法医遗传学实验室数量较少,无法全面评估 MPS 的局限性,但这项比较研究强调了 MPS 尽管生成了大量原始数据,但仍能产生可靠的图谱的能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/131b/10676315/ce93902798a2/11033_2023_8808_Fig1_HTML.jpg

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