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首页> 外文期刊>Forensic science international. Genetics >Thirty autosomal insertion-deletion polymorphisms analyzed using the Investigator (R) DIPplex Kit in populations from Iraq, Lithuania, Slovenia, and Turkey
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Thirty autosomal insertion-deletion polymorphisms analyzed using the Investigator (R) DIPplex Kit in populations from Iraq, Lithuania, Slovenia, and Turkey

机译:使用Investigator(R)DIPplex试剂盒分析了来自伊拉克,立陶宛,斯洛文尼亚和土耳其的人群的30种常染色体插入-缺失多态性

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Thirty autosomal insertion-deletion (InDel) polymorphisms were analyzed in four populations from Iraq, Lithuania, Slovenia, and Turkey using the commercial kit Investigator (R) DIPplex. Genotyping issues were encountered for five of the 30 InDels. They were most probably caused by polymorphisms located in the primer binding sites. Population and forensic parameters were calculated. No significant deviations from Hardy-Weinberg equilibrium or significant linkage disequilibrium were detected. The observed heterozygosities ranged from 33% to 61% depending on the marker and the population. The combined probability of exclusion for the 30 markers was 99.7% in all four populations and the matching probabilities were 1 in 3-4 x 10(12) individuals. The multidimensional scaling plot drawn from FST distances showed a good concordance between the relative position of the 15 populations included in the plot and their geographic locations. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
机译:使用商业试剂盒Investigator(R)DIPplex在来自伊拉克,立陶宛,斯洛文尼亚和土耳其的四个人群中分析了30个常染色体插入-缺失(InDel)多态性。 30个InDel中有五个遇到了基因分型问题。它们很可能是由位于引物结合位点的多态性引起的。计算人口和法医参数。没有发现与Hardy-Weinberg平衡有显着偏差或没有明显的连锁不平衡。观察到的杂合度在33%至61%之间,具体取决于标记和种群。在所有四个人群中,对30种标记物的排除总概率为99.7%,匹配概率为3-4 x 10(12)个个体中的1个。从FST距离绘制的多维比例尺图显示了该图中包括的15个人口的相对位置与其地理位置之间的良好一致性。 (C)2016 Elsevier Ireland Ltd.保留所有权利。

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