Willuweit Sascha, Roewer Lutz
Department of Forensic Genetics, Institute of Legal Medicine, Charité-Universitätsmedizin, Berlin, Germany.
Forensic Sci Int Genet. 2007 Jun;1(2):83-7. doi: 10.1016/j.fsigen.2007.01.017. Epub 2007 Mar 2.
The freely accessible YHRD (Y Chromosome Haplotype Reference Database, www.yhrd.org) is designed to store Y chromosome haplotypes from global populations and had replaced three earlier database versions collecting European, Asian and US American Y chromosomes separately. The focus is to disseminate haplotype frequency data to forensic analysts, researchers, and to everyone who is interested in historical and family genetics. YHRD considers reduction of the available number of polymorphisms on the Y chromosome to a uniform data string of 11 highly variable Y-STR loci as an efficient way to rapidly screen many world populations and to make their Y chromosome profiles comparable. Typing of the YHRD 11-locus core set is facilitated by commercial products, namely diagnostic PCR kits, and endorsed by scientific and forensic analyst's societies as ISFG or SWGDAM. YHRD is structured by the assignment of each submitted population sample to a set of populations sharing a common linguistic, demographic, genetic or geographic background (metapopulations). This principle facilitates the statistical evaluation of haplotype matches due to a significant enlargement of sample sizes. With the rapid growth of the database the definition of homogeneous metapopulations is now also feasible solely on the basis of the genetic data as exemplified for the whole dataset of YHRD, release 19 (August 2006). Large sample numbers within genetically defined metapopulations also allows the development of biostatistical methods to estimate the frequency of unobserved or rare haplotypes ("haplotype frequency surveying method"). Essential for the YHRD project is its collaborative character relying on the engagement of individual laboratories to make their data accessible via YHRD and to share the YHRD standards regarding data quality.
免费开放的YHRD(Y染色体单倍型参考数据库,www.yhrd.org)旨在存储全球人群的Y染色体单倍型,它取代了之前分别收集欧洲、亚洲和美国Y染色体的三个数据库版本。其重点是向法医分析师、研究人员以及所有对历史和家族遗传学感兴趣的人传播单倍型频率数据。YHRD认为,将Y染色体上可用的多态性数量减少为11个高度可变Y-STR基因座的统一数据串,是快速筛选众多世界人群并使他们的Y染色体图谱具有可比性的有效方法。商业产品,即诊断PCR试剂盒,便于对YHRD 11基因座核心集进行分型,并且得到了科学和法医分析师协会(如国际法医遗传学会或美国法医DNA分析科学工作组)的认可。YHRD通过将每个提交的人群样本分配到一组具有共同语言、人口统计学、遗传学或地理背景的人群(元种群)来构建。由于样本量显著增加,这一原则便于对单倍型匹配进行统计评估。随着数据库的快速增长,现在仅根据遗传数据来定义同质元种群也是可行的,如YHRD第19版(2006年8月)的整个数据集所示。基因定义的元种群中的大量样本数也使得开发生物统计学方法来估计未观察到或罕见单倍型的频率(“单倍型频率调查方法”)成为可能。YHRD项目的关键在于其协作性质,它依赖于各个实验室的参与,以便通过YHRD提供其数据,并共享有关数据质量的YHRD标准。