• 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

D5S2500是一个特征不明确的短串联重复序列:基因组时代法医微卫星的鉴定与描述。

D5S2500 is an ambiguously characterized STR: Identification and description of forensic microsatellites in the genomics age.

作者信息

Phillips C, Parson W, Amigo J, King J L, Coble M D, Steffen C R, Vallone P M, Gettings K B, Butler J M, Budowle B

机构信息

Forensic Genetics Unit, Institute of Forensic Sciences, University of Santiago de Compostela, Santiago de Compostela, Spain.

Institute of Legal Medicine, Medical University of Innsbruck, Innsbruck, Austria; Forensic Science Program, The Pennsylvania State University, PA, USA.

出版信息

Forensic Sci Int Genet. 2016 Jul;23:19-24. doi: 10.1016/j.fsigen.2016.03.002. Epub 2016 Mar 9.

DOI:10.1016/j.fsigen.2016.03.002
PMID:26974236
Abstract

In the process of establishing short tandem repeat (STR) sequence variant nomenclature guidelines in anticipation of expanded forensic multiplexes for massively parallel sequencing (MPS), it was discovered that the STR D5S2500 has multiple positions and genomic characteristics reported. This ambiguity is because the marker named D5S2500 consists of two different microsatellites forming separate components in the capillary electrophoresis multiplexes of Qiagen's HDplex (Hilden, Germany) and AGCU ScienTech's non-CODIS STR 21plex (Wuxi, Jiangsu, China). This study outlines the genomic details used to identify each microsatellite and reveals the D5S2500 marker in HDplex has the correctly assigned STR name, while the D5S2500 marker in the AGCU 21plex, closely positioned a further 1643 nucleotides in the human reference sequence, is an unnamed microsatellite. The fact that the D5S2500 marker has existed as two distinct STR loci undetected for almost ten years, even with reported discordant genotypes for the standard control DNA, underlines the need for careful scrutiny of the genomic properties of forensic STRs, as they become adapted for sequence analysis with MPS systems. We make the recommendation that precise chromosome location data must be reported for any forensic marker under development but not in common use, so that the genomic characteristics of the locus are validated to the same level of accuracy as its allelic variation and forensic performance. To clearly differentiate each microsatellite, we propose the name D5S2800 be used to identify the Chromosome-5 STR in the AGCU 21plex.

摘要

在为大规模平行测序(MPS)建立扩展法医多重检测的短串联重复序列(STR)序列变异命名指南的过程中,发现STR D5S2500有多个已报道的位置和基因组特征。这种模糊性是因为名为D5S2500的标记由两个不同的微卫星组成,在Qiagen公司的HDplex(德国希尔德)和AGCU ScienTech公司的非CODIS STR 21plex(中国江苏无锡)的毛细管电泳多重检测中形成单独的组分。本研究概述了用于识别每个微卫星的基因组细节,并揭示HDplex中的D5S2500标记具有正确指定的STR名称,而AGCU 21plex中的D5S2500标记在人类参考序列中进一步定位了1643个核苷酸,是一个未命名的微卫星。即使标准对照DNA的基因型存在不一致报道,D5S2500标记作为两个不同的STR位点未被检测到近十年这一事实,强调了在法医STR适应MPS系统进行序列分析时,仔细审查其基因组特性的必要性。我们建议,对于任何正在开发但尚未普遍使用的法医标记,必须报告精确的染色体定位数据,以便将该位点的基因组特征验证到与其等位基因变异和法医性能相同的准确水平。为了清楚地区分每个微卫星,我们建议使用名称D5S2800来识别AGCU 21plex中的5号染色体STR。

相似文献

1
D5S2500 is an ambiguously characterized STR: Identification and description of forensic microsatellites in the genomics age.D5S2500是一个特征不明确的短串联重复序列:基因组时代法医微卫星的鉴定与描述。
Forensic Sci Int Genet. 2016 Jul;23:19-24. doi: 10.1016/j.fsigen.2016.03.002. Epub 2016 Mar 9.
2
Massively parallel sequencing of forensic STRs: Considerations of the DNA commission of the International Society for Forensic Genetics (ISFG) on minimal nomenclature requirements.法医 STRs 的大规模平行测序:国际法医遗传学会(ISFG)DNA 委员会关于最小命名要求的考虑。
Forensic Sci Int Genet. 2016 May;22:54-63. doi: 10.1016/j.fsigen.2016.01.009. Epub 2016 Jan 21.
3
Filipino DNA variation at 12 X-chromosome short tandem repeat markers.菲律宾人在 12 个 X 染色体短串联重复标记处的 DNA 变异。
Forensic Sci Int Genet. 2018 Sep;36:e8-e12. doi: 10.1016/j.fsigen.2018.06.008. Epub 2018 Jun 8.
4
A newly devised multiplex assay of novel polymorphic non-CODIS STRs as a valuable tool for forensic application.一种新设计的多聚酶链反应复合扩增检测新型多态性非 CODIS STR 基因座的方法,可作为法庭科学应用的有效工具。
Forensic Sci Int Genet. 2020 Sep;48:102341. doi: 10.1016/j.fsigen.2020.102341. Epub 2020 Jun 20.
5
Investigator HDplex (Qiagen) reference population database for forensic use in Argentina.用于阿根廷法医鉴定的Investigator HDplex(Qiagen)参考人群数据库。
Forensic Sci Int Genet. 2017 Jan;26:91-95. doi: 10.1016/j.fsigen.2016.10.009. Epub 2016 Oct 18.
6
A genomic audit of newly-adopted autosomal STRs for forensic identification.用于法医鉴定的新采用常染色体短串联重复序列的基因组审计。
Forensic Sci Int Genet. 2017 Jul;29:193-204. doi: 10.1016/j.fsigen.2017.04.011. Epub 2017 Apr 23.
7
Performance and concordance of the ForenSeq™ system for autosomal and Y chromosome short tandem repeat sequencing of reference-type specimens.ForenSeq™系统对参考型样本进行常染色体和Y染色体短串联重复序列测序的性能及一致性
Forensic Sci Int Genet. 2017 May;28:1-9. doi: 10.1016/j.fsigen.2017.01.001. Epub 2017 Jan 9.
8
Developmental validation of the AGCU 21+1 STR kit: a novel multiplex assay for forensic application.AGCU 21+1 STR试剂盒的发育验证:一种用于法医应用的新型多重检测方法。
Electrophoresis. 2015 Jan;36(2):271-6. doi: 10.1002/elps.201400333. Epub 2014 Dec 17.
9
Massively parallel sequencing of 17 commonly used forensic autosomal STRs and amelogenin with small amplicons.采用小扩增子对 17 个常用法医常染色体 STR 和 amelogenin 进行大规模平行测序。
Forensic Sci Int Genet. 2016 May;22:1-7. doi: 10.1016/j.fsigen.2016.01.001. Epub 2016 Jan 8.
10
Development of a novel forensic STR multiplex for ancestry analysis and extended identity testing.开发一种新型法医 STR 复合扩增试剂盒用于谱系分析和扩展身份检测
Electrophoresis. 2013 Apr;34(8):1151-62. doi: 10.1002/elps.201200621. Epub 2013 Mar 18.

引用本文的文献

1
Development and validation of a novel 133-plex forensic STR panel (52 STRs and 81 Y-STRs) using single-end 400 bp massive parallel sequencing.使用单端400bp大规模平行测序技术开发并验证一种新型的133重法医STR检测试剂盒(52个常染色体STR和81个Y染色体STR)
Int J Legal Med. 2022 Mar;136(2):447-464. doi: 10.1007/s00414-021-02738-1. Epub 2021 Nov 6.
2
The STRidER Report on Two Years of Quality Control of Autosomal STR Population Datasets.STRidER 报告:两年常染色体 STR 群体数据集的质量控制。
Genes (Basel). 2020 Aug 7;11(8):901. doi: 10.3390/genes11080901.
3
An evaluation of the SureID 23comp Human Identification Kit for kinship testing.
SureID 23comp 人类识别试剂盒在亲缘关系测试中的评估。
Sci Rep. 2019 Nov 14;9(1):16859. doi: 10.1038/s41598-019-52838-7.
4
Impact of DNA degradation on massively parallel sequencing-based autosomal STR, iiSNP, and mitochondrial DNA typing systems.基于大规模平行测序的常染色体 STR、iiSNP 和线粒体 DNA 分型系统中 DNA 降解的影响。
Int J Legal Med. 2019 Sep;133(5):1369-1380. doi: 10.1007/s00414-019-02110-4. Epub 2019 Jul 2.
5
A novel multiplex assay of SNP-STR markers for forensic purpose.用于法医目的的 SNP-STR 标记的新型多重分析。
PLoS One. 2018 Jul 18;13(7):e0200700. doi: 10.1371/journal.pone.0200700. eCollection 2018.