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使用 Verogen 的 ForenSeq DNA Signature Prep Kit 和 MinION 对 STR 和 SNPs 进行法医纳米孔测序。

Forensic nanopore sequencing of STRs and SNPs using Verogen's ForenSeq DNA Signature Prep Kit and MinION.

机构信息

Beijing Institute of Radiation Medicine, Beijing, 100850, People's Republic of China.

School of Forensic Medicine, Shanxi Medical University, Taiyuan, 030001, People's Republic of China.

出版信息

Int J Legal Med. 2021 Sep;135(5):1685-1693. doi: 10.1007/s00414-021-02604-0. Epub 2021 May 5.

Abstract

The MinION nanopore sequencing device (Oxford Nanopore Technologies, Oxford, UK) is the smallest commercially available sequencer and can be used outside of conventional laboratories. The use of the MinION for forensic applications, however, is hindered by the high error rate of nanopore sequencing. One approach to solving this problem is to identify forensic genetic markers that can consistently be typed correctly based on nanopore sequencing. In this pilot study, we explored the use of nanopore sequencing for single nucleotide polymorphism (SNP) and short tandem repeat (STR) profiling using Verogen's (San Diego, CA, USA) ForenSeq DNA Signature Prep Kit. Thirty single-contributor samples and DNA standard material 2800 M were genotyped using the Illumina (San Diego, CA, USA) MiSeq FGx and MinION (with R9.4.1 flow cells) devices. With an optimized cutoff for allelic imbalance, all 94 identity-informative SNP loci could be genotyped reliably using the MinION device, with an overall accuracy of 99.958% (1 error among 2926 genotypes). STR typing was notably error prone, and its accuracy was locus dependent. We developed a custom-made bioinformatics workflow, and finally selected 13 autosomal STRs, 14 Y-STRs, and 4 X-STRs showing high consistency between nanopore and Illumina sequencing among the tested samples. These SNP and STR loci could be candidates for panel design for forensic analysis based on nanopore sequencing.

摘要

MinION 纳米孔测序仪(Oxford Nanopore Technologies,英国牛津)是目前市面上最小的商业化测序仪,可在常规实验室以外使用。然而,由于纳米孔测序的错误率较高,该仪器在法医应用中受到限制。解决这个问题的一种方法是,根据纳米孔测序确定能够始终正确分型的法医遗传标记。在这项初步研究中,我们使用 Verogen 的(美国加利福尼亚州圣地亚哥)ForenSeq DNA Signature Prep 试剂盒探索了纳米孔测序在单核苷酸多态性(SNP)和短串联重复序列(STR)分析中的应用。使用 Illumina(美国加利福尼亚州圣地亚哥)MiSeq FGx 和 MinION(配备 R9.4.1 流动池)设备对 30 个单份样本和 DNA 标准物质 2800M 进行了基因分型。通过优化等位基因失衡的截断值,使用 MinION 设备可以可靠地对 94 个身份信息 SNP 基因座进行基因分型,总体准确率为 99.958%(2926 个基因型中有 1 个错误)。STR 基因分型明显容易出错,且其准确性取决于基因座。我们开发了一种定制的生物信息学工作流程,并最终选择了 13 个常染色体 SNP、14 个 Y-STR 和 4 个 X-STR,这些 SNP 和 STR 基因座在经过测试的样本中显示出纳米孔和 Illumina 测序之间的高度一致性。这些 SNP 和 STR 基因座可作为基于纳米孔测序的法医分析面板设计的候选基因座。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5291/8098014/e8b10b417fc1/414_2021_2604_Fig1_HTML.jpg

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