• 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

EDNAP小组关于以聚合酶链反应五重分析形式对Y染色体短串联重复序列DYS19、DYS389 I和II、DYS390及DYS393的再现性和稳定性的一项合作研究结果。

Results of a collaborative study of the EDNAP group regarding the reproducibility and robustness of the Y-chromosome STRs DYS19, DYS389 I and II, DYS390 and DYS393 in a PCR pentaplex format.

作者信息

Carracedo A, Beckmann A, Bengs A, Brinkmann B, Caglia A, Capelli C, Gill P, Gusmão L, Hagelberg C, Hohoff C, Hoste B, Kihlgren A, Kloosterman A, Myhre Dupuy B, Morling N, O'Donnell G, Parson W, Phillips C, Pouwels M, Scheithauer R, Schmitter H, Schneider P M, Schumm J, Skitsa I, Stradmann-Bellinghausen B, Stuart M, Syndercombe Court D, Vide C

机构信息

Institute of Legal Medicine, Faculty of Medicine 15705 Santiago de Compostela, Galicia, Spain.

出版信息

Forensic Sci Int. 2001 Jun 1;119(1):28-41. doi: 10.1016/s0379-0738(00)00395-9.

DOI:10.1016/s0379-0738(00)00395-9
PMID:11348791
Abstract

A collaborative exercise was carried out by the European DNA Profiling Group (EDNAP) in the frame work of the STADNAP program, i.e. standardization of DNA profiling in Europe, in order to evaluate the performance of a Y-chromosome STR pentaplex, which includes the loci DYS19, DYS389 I and II, DYS390 and DYS393 and to determine whether uniformity of results could be achieved among different European laboratories. Laboratories were asked to analyze the five Y-STRs using singleplex and multiplex conditions in three bloodstains and one mixed stain (95% female and 5% male). All the laboratories reported the same results even for the mixed stain included in the exercise. This demonstrates the reproducibility and robustness of Y-chromosome STR typing even with multiplex formats and proves the usefulness of Y-STR systems for analyzing mixed stains with a male component.A total of 930 male samples from 10 different populations from Europe were also analysed for all the loci included in the pentaplex. Eight of these ten populations also included haplotype data. As for single gene analysis, haplotype diversity was higher in Germany and Italy and lower in Western European countries and Finland. Pairwise haplotype analysis shows the Finnish departure from the rest of the populations and a relatively homogeneity in the other European populations with F(ST) estimates lower than 0.05.UPGMA analysis shows an association of Western European population (Ireland, UK, Portugal and Galicia) on the one hand and central European populations on the other.

摘要

欧洲DNA分析小组(EDNAP)在STADNAP项目(即欧洲DNA分析标准化项目)框架内开展了一项合作活动,以评估包含DYS19、DYS389 I和II、DYS390以及DYS393基因座的Y染色体STR五重试剂盒的性能,并确定不同欧洲实验室之间能否实现结果的一致性。要求各实验室在三种血迹样本和一种混合样本(95%为女性,5%为男性)中使用单重和多重条件分析这五个Y-STR。即使对于此次活动中包含的混合样本,所有实验室报告的结果也相同。这证明了即使采用多重检测形式,Y染色体STR分型仍具有可重复性和稳健性,并证明了Y-STR系统在分析含有男性成分的混合样本方面的实用性。还对来自欧洲10个不同人群的总共930份男性样本进行了该五重试剂盒中所有基因座的分析。这10个人群中有8个还包含单倍型数据。就单基因分析而言,德国和意大利的单倍型多样性较高,而在西欧国家和芬兰则较低。成对单倍型分析显示芬兰与其他人群存在差异,而其他欧洲人群相对同质,F(ST)估计值低于0.05。UPGMA分析显示,一方面是西欧人群(爱尔兰、英国、葡萄牙和加利西亚),另一方面是中欧人群,二者存在关联。

相似文献

1
Results of a collaborative study of the EDNAP group regarding the reproducibility and robustness of the Y-chromosome STRs DYS19, DYS389 I and II, DYS390 and DYS393 in a PCR pentaplex format.EDNAP小组关于以聚合酶链反应五重分析形式对Y染色体短串联重复序列DYS19、DYS389 I和II、DYS390及DYS393的再现性和稳定性的一项合作研究结果。
Forensic Sci Int. 2001 Jun 1;119(1):28-41. doi: 10.1016/s0379-0738(00)00395-9.
2
Robustness of the Y STRs DYS19, DYS389 I and II, DYS390 and DYS393: optimization of a PCR pentaplex.Y染色体短串联重复序列DYS19、DYS389 I和II、DYS390及DYS393的稳定性:聚合酶链式反应五重扩增的优化
Forensic Sci Int. 1999 Dec 20;106(3):163-72. doi: 10.1016/s0379-0738(99)00187-5.
3
Results of collaborative study regarding the standardization of the Y-linked STR system DYS385 by the European DNA Profiling (EDNAP) group.
Forensic Sci Int. 1999 Jun 28;102(2-3):159-65. doi: 10.1016/s0379-0738(99)00049-3.
4
Haplotype frequencies and population data of nine Y-chromosomal STR polymorphisms in a German and a Chinese population.德国和中国人群中9个Y染色体STR多态性的单倍型频率及群体数据。
Forensic Sci Int. 2000 Sep 11;113(1-3):47-53. doi: 10.1016/s0379-0738(00)00261-9.
5
Y chromosomal short tandem repeat (STR) loci in a representative group of males living in South Württemberg: a database for application in forensic medicine.居住在符腾堡南部的一组具有代表性男性群体中的Y染色体短串联重复序列(STR)基因座:一个应用于法医学的数据库。
Forensic Sci Int. 2000 Sep 11;113(1-3):43-6. doi: 10.1016/s0379-0738(00)00195-x.
6
Population studies of the Y-chromosome specific polymorphisms DYS19, DYS389 I + II, DYS390 and DYS393 in a western German population (Bonn area).对德国西部人群(波恩地区)Y染色体特异性多态性DYS19、DYS389 I + II、DYS390和DYS393的群体研究。
Forensic Sci Int. 1999 May 17;101(3):195-201. doi: 10.1016/s0379-0738(99)00029-8.
7
Y-chromosomal STR haplotypes in a population sample from Bavaria.巴伐利亚人群样本中的Y染色体短串联重复序列单倍型
Int J Legal Med. 2000;113(3):189-92. doi: 10.1007/s004140050296.
8
Y-STR haplotyping in two Hungarian populations.匈牙利两个群体中的Y染色体短串联重复序列单倍型分型
Int J Legal Med. 1999;113(1):38-42. doi: 10.1007/s004140050276.
9
Y-chromosome STR haplotypes from a Western Mediterranean population sample.来自西地中海人群样本的Y染色体短串联重复单倍型
Forensic Sci Int. 2001 Jun 15;119(2):254-7. doi: 10.1016/s0379-0738(00)00432-1.
10
Y-chromosome STR haplotype profiling in the Korean population.韩国人群的Y染色体短串联重复序列单倍型分析
Forensic Sci Int. 2001 Jan 15;115(3):231-7. doi: 10.1016/s0379-0738(00)00332-7.

引用本文的文献

1
Infant mortality and ethnicity in an indigenous European population: novel evidence from the Finnish population register.欧洲本土人口中的婴儿死亡率与种族:来自芬兰人口登记册的新证据
Sci Rep. 2014 Feb 27;4:4214. doi: 10.1038/srep04214.
2
Development and validation of a multiplex reaction analyzing eight miniSTRs of the X chromosome for identity and kinship testing with degraded DNA.开发并验证了一种多重反应分析试剂盒,可分析 X 染色体上的 8 个微 STR 用于降解 DNA 的个体识别和亲缘关系鉴定。
Int J Legal Med. 2013 Jul;127(4):735-9. doi: 10.1007/s00414-012-0795-2. Epub 2012 Nov 28.
3
Mutations or exclusion: an unusual case in paternity testing.
突变或排除:亲子鉴定中的一个特殊案例。
Int J Legal Med. 2006 Nov;120(6):360-3. doi: 10.1007/s00414-005-0045-y. Epub 2005 Nov 19.
4
Finnish Disease Heritage II: population prehistory and genetic roots of Finns.芬兰疾病遗产II:芬兰人的人口史前史与基因根源
Hum Genet. 2003 May;112(5-6):457-69. doi: 10.1007/s00439-002-0876-2. Epub 2003 Mar 8.