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首页> 外文期刊>International Journal of Legal Medicine >Combining results of forensic STR kits: HDplex validation including allelic association and linkage testing with NGM and Identifiler loci
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Combining results of forensic STR kits: HDplex validation including allelic association and linkage testing with NGM and Identifiler loci

机译:法医STR试剂盒的组合结果:HDplex验证,包括等位基因关联和与NGM和Identifiler基因座的连锁测试

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摘要

The autosomal short tandem repeat (STR) kits that are currently used in forensic science have a high discrimination power. However, this discrimination power is sometimes not sufficient for complex kinship analyses or decreases when alleles are missing due to degradation of the DNA. The Investigator HDplex kit contains nine STRs that are additional to the commonly used forensic markers, and we validated this kit to assist human identification. With the increasing number of markers it becomes inevitable that forensic and kinship analyses include two or more STRs present on the same chromosome. To examine whether such markers can be regarded as independent, we evaluated the 30 STRs present in NGM, Identifiler and HDplex. Among these 30 markers, 17 syntenic STR pairs can be formed. Allelic association between these pairs was examined using 335 Dutch reference samples and no linkage disequilibrium was detected, which makes it possible to use the product rule for profile probability calculations in unrelated individuals. Linkage between syntenic STRs was studied by determining the recombination fraction between them in five three-generation CEPH families. The recombination fractions were compared to the physical and genetic distances between the markers. For most types of pedigrees, the kinship analyses can be performed using the product rule, and for those cases that require an alternative calculation method (Gill et al., Forensic Sci Int Genet 6:477–486, 2011), the recombination fractions as determined in this study can be used. Finally, we calculated the (combined) match probabilities, for the supplementary genotyping results of HDplex, NGM and Identifiler.
机译:目前在法医科学中使用的常染色体短串联重复序列(STR)试剂盒具有很高的辨别力。但是,这种区分能力有时不足以进行复杂的亲缘关系分析,或者由于DNA的降解而导致等位基因缺失时,这种区分能力会降低。 Investigator HDplex试剂盒包含九种STR,是常用的法医标记物之外的另一种,我们验证了该试剂盒有助于人类识别。随着标记物数量的增加,法医和亲属关系分析不可避免地要包括存在于同一条染色体上的两个或多个STR。为了检查此类标记是否可以视为独立标记,我们评估了NGM,Identifiler和HDplex中存在的30个STR。在这30个标记中,可以形成17个同义STR对。使用335个荷兰参考样本检查了这些对之间的等位基因关联,未检测到连锁不平衡,这使得可以使用乘积规则来计算无关个体中的概貌概率。通过确定五个三代CEPH家族中同构STR之间的重组比例,研究了同构STR之间的联系。将重组级分与标记之间的物理和遗传距离进行比较。对于大多数类型的谱系,可以使用乘积规则进行亲缘关系分析,对于需要替代计算方法的情况(Gill等人,Forensic Sc​​i Int Genet 6:477–486,2011),重组分数为在这项研究中确定可以使用。最后,我们为HDplex,NGM和Identifiler的补充基因分型结果计算了(组合的)匹配概率。

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