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一项由全球卫生流行病学合作组织(GHEP)与国际法医遗传学会(ISFG)开展的关于38个常染色体插入缺失(indel)基因变异用于不同大陆人群身份识别的合作研究。

A GHEP-ISFG collaborative study on the genetic variation of 38 autosomal indels for human identification in different continental populations.

作者信息

Pereira R, Alves C, Aler M, Amorim A, Arévalo C, Betancor E, Braganholi D, Bravo M L, Brito P, Builes J J, Burgos G, Carvalho E F, Castillo A, Catanesi C I, Cicarelli R M B, Coufalova P, Dario P, D'Amato M E, Davison S, Ferragut J, Fondevila M, Furfuro S, García O, Gaviria A, Gomes I, González E, Gonzalez-Liñan A, Gross T E, Hernández A, Huang Q, Jiménez S, Jobim L F, López-Parra A M, Marino M, Marques S, Martínez-Cortés G, Masciovecchio V, Parra D, Penacino G, Pinheiro M F, Porto M J, Posada Y, Restrepo C, Ribeiro T, Rubio L, Sala A, Santurtún A, Solís L S, Souto L, Streitemberger E, Torres A, Vilela-Lamego C, Yunis J J, Yurrebaso I, Gusmão L

机构信息

IPATIMUP (Institute of Molecular Pathology and Immunology of the University of Porto), Porto, Portugal; I3 s (Instituto de Investigação e Inovação em Saúde, Universidade do Porto), Porto, Portugal.

IPATIMUP (Institute of Molecular Pathology and Immunology of the University of Porto), Porto, Portugal; I3 s (Instituto de Investigação e Inovação em Saúde, Universidade do Porto), Porto, Portugal.

出版信息

Forensic Sci Int Genet. 2018 Jan;32:18-25. doi: 10.1016/j.fsigen.2017.09.012. Epub 2017 Sep 22.

Abstract

A collaborative effort was carried out by the Spanish and Portuguese Speaking Working Group of the International Society for Forensic Genetics (GHEP-ISFG) to promote knowledge exchange between associate laboratories interested in the implementation of indel-based methodologies and build allele frequency databases of 38 indels for forensic applications. These databases include populations from different countries that are relevant for identification and kinship investigations undertaken by the participating laboratories. Before compiling population data, participants were asked to type the 38 indels in blind samples from annual GHEP-ISFG proficiency tests, using an amplification protocol previously described. Only laboratories that reported correct results contributed with population data to this study. A total of 5839 samples were genotyped from 45 different populations from Africa, America, East Asia, Europe and Middle East. Population differentiation analysis showed significant differences between most populations studied from Africa and America, as well as between two Asian populations from China and East Timor. Low F values were detected among most European populations. Overall diversities and parameters of forensic efficiency were high in populations from all continents.

摘要

国际法医遗传学协会西班牙语和葡萄牙语工作组(GHEP - ISFG)开展了一项合作努力,以促进对基于插入缺失方法实施感兴趣的关联实验室之间的知识交流,并建立用于法医应用的38个插入缺失的等位基因频率数据库。这些数据库包括来自不同国家的人群,这些人群与参与实验室进行的身份鉴定和亲属关系调查相关。在汇编人群数据之前,要求参与者使用先前描述的扩增方案,对来自年度GHEP - ISFG能力验证测试的盲样中的38个插入缺失进行分型。只有报告正确结果的实验室才为本研究提供人群数据。共对来自非洲、美洲、东亚、欧洲和中东的45个不同人群的5839个样本进行了基因分型。群体分化分析显示,大多数来自非洲和美洲的研究人群之间以及来自中国和东帝汶的两个亚洲人群之间存在显著差异。在大多数欧洲人群中检测到低F值。所有大陆人群的总体多样性和法医效率参数都很高。

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