• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

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.

DOI:10.1007/s00414-021-02604-0
PMID:33950286
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8098014/
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/f40148f491fe/414_2021_2604_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5291/8098014/e8b10b417fc1/414_2021_2604_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5291/8098014/29a3f754c27c/414_2021_2604_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5291/8098014/f40148f491fe/414_2021_2604_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5291/8098014/e8b10b417fc1/414_2021_2604_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5291/8098014/29a3f754c27c/414_2021_2604_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5291/8098014/f40148f491fe/414_2021_2604_Fig3_HTML.jpg

相似文献

1
Forensic nanopore sequencing of STRs and SNPs using Verogen's ForenSeq DNA Signature Prep Kit and MinION.使用 Verogen 的 ForenSeq DNA Signature Prep Kit 和 MinION 对 STR 和 SNPs 进行法医纳米孔测序。
Int J Legal Med. 2021 Sep;135(5):1685-1693. doi: 10.1007/s00414-021-02604-0. Epub 2021 May 5.
2
Nanopore sequencing of forensic short tandem repeats using QNome of Qitan Technology.利用齐碳科技的 QNome 对法医短串联重复序列进行纳米孔测序。
Electrophoresis. 2024 Sep;45(17-18):1535-1545. doi: 10.1002/elps.202300270. Epub 2024 Jun 17.
3
Massively parallel sequencing of forensic STRs and SNPs using the Illumina ForenSeq™ DNA Signature Prep Kit on the MiSeq FGx™ Forensic Genomics System.使用Illumina ForenSeq™ DNA签名制备试剂盒在MiSeq FGx™法医基因组系统上对法医STR和SNP进行大规模平行测序。
Forensic Sci Int Genet. 2017 Nov;31:135-148. doi: 10.1016/j.fsigen.2017.09.003. Epub 2017 Sep 8.
4
Developmental validation of the MiSeq FGx Forensic Genomics System for Targeted Next Generation Sequencing in Forensic DNA Casework and Database Laboratories.MiSeq FGx法医基因组学系统在法医DNA案件工作和数据库实验室中用于靶向新一代测序的发育验证。
Forensic Sci Int Genet. 2017 May;28:52-70. doi: 10.1016/j.fsigen.2017.01.011. Epub 2017 Jan 27.
5
Accurate profiling of forensic autosomal STRs using the Oxford Nanopore Technologies MinION device.利用牛津纳米孔技术 MinION 设备对法医常染色体 STR 进行准确分析。
Forensic Sci Int Genet. 2022 Jan;56:102629. doi: 10.1016/j.fsigen.2021.102629. Epub 2021 Nov 17.
6
Nanopore Sequencing of a Forensic STR Multiplex Reveals Loci Suitable for Single-Contributor STR Profiling.法医STR复合扩增的纳米孔测序揭示了适用于单供体STR分型的基因座。
Genes (Basel). 2020 Apr 1;11(4):381. doi: 10.3390/genes11040381.
7
Global patterns of STR sequence variation: Sequencing the CEPH human genome diversity panel for 58 forensic STRs using the Illumina ForenSeq DNA Signature Prep Kit.全球 STR 序列变异模式:使用 Illumina ForenSeq DNA Signature Prep Kit 对 CEPH 人类基因组多样性面板进行 58 个法医 STR 测序。
Electrophoresis. 2018 Nov;39(21):2708-2724. doi: 10.1002/elps.201800117. Epub 2018 Sep 3.
8
Evaluation of the Illumina ForenSeq™ DNA Signature Prep Kit - MPS forensic application for the MiSeq FGx™ benchtop sequencer.Illumina ForenSeq™ DNA 特征制备试剂盒在 MiSeq FGx™ 台式测序仪上的法医应用评估。
Forensic Sci Int Genet. 2017 May;28:188-194. doi: 10.1016/j.fsigen.2017.02.018. Epub 2017 Mar 1.
9
A closer look at Verogen's Forenseq™ DNA Signature Prep kit autosomal and Y-STR data for streamlined analysis of routine reference samples.深入了解 Verogen 的 Forenseq™ DNA Signature Prep 试剂盒的常染色体和 Y-STR 数据,以实现常规参考样本的简化分析。
Electrophoresis. 2018 Nov;39(21):2685-2693. doi: 10.1002/elps.201800087. Epub 2018 Aug 12.
10
Pilot validation of on-field STR typing and human identity testing by MinION nanopore sequencing.通过MinION纳米孔测序进行现场STR分型和人类身份测试的初步验证。
Electrophoresis. 2024 May;45(9-10):885-896. doi: 10.1002/elps.202300234. Epub 2024 Feb 14.

引用本文的文献

1
Sequencing the orthologs of human autosomal forensic short tandem repeats provides individual- and species-level identification in African great apes.对人类常染色体法医短串联重复序列的同源基因进行测序,可在非人类的大型猿类中进行个体和物种水平的鉴定。
BMC Ecol Evol. 2024 Oct 31;24(1):134. doi: 10.1186/s12862-024-02324-0.
2
NASTRA: accurate analysis of short tandem repeat markers by nanopore sequencing with repeat-structure-aware algorithm.NASTRA:利用具有重复结构感知算法的纳米孔测序技术对短串联重复标记进行精确分析。
Brief Bioinform. 2024 Sep 23;25(6). doi: 10.1093/bib/bbae472.
3
Forensic DNA phenotyping using Oxford Nanopore Sequencing system.

本文引用的文献

1
Developmental Validation of the ANDE 6C System for Rapid DNA Analysis of Forensic Casework and DVI Samples.法医生物检材和 DVI 样本快速 DNA 分析的 ANDE 6C 系统的开发验证。
J Forensic Sci. 2020 Jul;65(4):1056-1071. doi: 10.1111/1556-4029.14286. Epub 2020 Feb 10.
2
Human short tandem repeat identification using a nanopore-based DNA sequencer: a pilot study.利用基于纳米孔的 DNA 测序仪进行人类短串联重复序列鉴定:一项初步研究。
J Hum Genet. 2020 Jan;65(1):21-24. doi: 10.1038/s10038-019-0688-z. Epub 2019 Oct 24.
3
Developmental validation of the ANDE™ rapid DNA system with FlexPlex™ assay for arrestee and reference buccal swab processing and database searching.
使用牛津纳米孔测序系统进行法医DNA表型分析。
Electrophoresis. 2025 Feb;46(3-4):198-211. doi: 10.1002/elps.202300252. Epub 2024 May 25.
4
PHARE: a bioinformatics pipeline for compositional profiling of multiclonal Plasmodium falciparum infections from long-read Nanopore sequencing data.PHARE:一种生物信息学管道,用于从长读长 Nanopore 测序数据中对多克隆恶性疟原虫感染进行组成谱分析。
J Antimicrob Chemother. 2024 May 2;79(5):987-996. doi: 10.1093/jac/dkae060.
5
A novel 193-plex MPS panel integrating STRs and SNPs highlights the application value of forensic genetics in individual identification and paternity testing.一种新型的 193 重复合扩增试剂盒(MPS)面板,集成了 STRs 和 SNPs,突出了法医学遗传学在个体识别和亲子鉴定中的应用价值。
Hum Genet. 2024 Mar;143(3):371-383. doi: 10.1007/s00439-024-02658-1. Epub 2024 Mar 18.
6
The Revolution of Animal Genomics in Forensic Sciences.动物基因组学在法医学中的革命。
Int J Mol Sci. 2023 May 16;24(10):8821. doi: 10.3390/ijms24108821.
7
An Introduction to Nanopore Sequencing: Past, Present, and Future Considerations.纳米孔测序简介:过去、现在及未来考量
Micromachines (Basel). 2023 Feb 16;14(2):459. doi: 10.3390/mi14020459.
8
Recent advances in forensic biology and forensic DNA typing: INTERPOL review 2019-2022.法医生物学和法医DNA分型的最新进展:国际刑警组织2019 - 2022年综述
Forensic Sci Int Synerg. 2022 Dec 27;6:100311. doi: 10.1016/j.fsisyn.2022.100311. eCollection 2023.
9
Estimating individual mtDNA haplotypes in mixed DNA samples by combining MinION and MiSeq.利用 MinION 和 MiSeq 组合估算混合 DNA 样本中的个体 mtDNA 单倍型。
Int J Legal Med. 2022 Mar;136(2):423-432. doi: 10.1007/s00414-021-02763-0. Epub 2022 Jan 10.
10
Nanopore Technology and Its Applications in Gene Sequencing.纳米孔技术及其在基因测序中的应用。
Biosensors (Basel). 2021 Jun 30;11(7):214. doi: 10.3390/bios11070214.
与 FlexPlex™ 检测试剂盒联合应用,对被捕者和参考者口腔拭子处理和数据库搜索的 ANDE™ 快速 DNA 系统的开发验证。
Forensic Sci Int Genet. 2019 May;40:120-130. doi: 10.1016/j.fsigen.2019.02.016. Epub 2019 Feb 19.
4
Forensic tri-allelic SNP genotyping using nanopore sequencing.利用纳米孔测序进行法医三等位基因 SNP 基因分型。
Forensic Sci Int Genet. 2019 Jan;38:204-210. doi: 10.1016/j.fsigen.2018.11.012. Epub 2018 Nov 12.
5
Minimap2: pairwise alignment for nucleotide sequences.Minimap2:核苷酸序列的两两比对。
Bioinformatics. 2018 Sep 15;34(18):3094-3100. doi: 10.1093/bioinformatics/bty191.
6
Unbiased Strain-Typing of Arbovirus Directly from Mosquitoes Using Nanopore Sequencing: A Field-forward Biosurveillance Protocol.基于纳米孔测序的蚊虫中虫媒病毒无偏性血清型分析:一种现场前瞻性的生物监测方案。
Sci Rep. 2018 Apr 3;8(1):5417. doi: 10.1038/s41598-018-23641-7.
7
A 472-SNP panel for pairwise kinship testing of second-degree relatives.用于二级亲属亲缘关系检测的 472-SNP 面板。
Forensic Sci Int Genet. 2018 May;34:178-185. doi: 10.1016/j.fsigen.2018.02.019. Epub 2018 Mar 2.
8
Nanopore sequencing and assembly of a human genome with ultra-long reads.纳米孔测序和超长读长组装人类基因组。
Nat Biotechnol. 2018 Apr;36(4):338-345. doi: 10.1038/nbt.4060. Epub 2018 Jan 29.
9
On site DNA barcoding by nanopore sequencing.通过纳米孔测序进行现场DNA条形码分析。
PLoS One. 2017 Oct 4;12(10):e0184741. doi: 10.1371/journal.pone.0184741. eCollection 2017.
10
Multiplex PCR method for MinION and Illumina sequencing of Zika and other virus genomes directly from clinical samples.用于直接从临床样本中对寨卡病毒及其他病毒基因组进行MinION和Illumina测序的多重PCR方法。
Nat Protoc. 2017 Jun;12(6):1261-1276. doi: 10.1038/nprot.2017.066. Epub 2017 May 24.