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Diversity of nuclear short tandem repeat loci in representative sample of North-eastern Bosnian and Herzegovina population

机译:波斯尼亚和黑塞哥维那东北部人口代表性样本中核短串联重复基因座的多样性

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Diversity of nuclear microsatellite markers were analyzed in a reference sample of the population of northeast Bosnia and Herzegovina. 437 samples taken from unrelated individuals were processed and three samples of paternity proof were shown. Detection effectiveness profile of the research, points to a valid choice of method of extraction, amplification and genotyping short tandem repeat (STR) loci with PowerPlextm16 kit. Genetic analysis of allelic variants of the 15 STR loci PowerPlextm16 kit detected 17 samples determined as rare allelic variants or microvariants. Samples were divided into 15 different allelic variants at 7 different loci, and are: in locus D7S820, D16S539, D3S1358, D18S51, PENTA D, PENTA E and in locus vWA. Genetic analysis of mutations in cases of paternity determined three examples of single-step mutations in the loci FGA, Penta D and D3S1358. Genetic analysis of observed STR loci detected three allelic variant of genotype combination 7/10/11.3 in locus D7S820 Type II. Population genetic analysis of STR loci in a representative sample of the population of northeast Bosnia and Herzegovina included the application of the assessment tests of within-population genetic diversity and interpopulation diversity, as well as genetic differentiation between populations: North-eastern Bosnia and Herzegovina (BH) and BH general reference, then the Croatian population, Macedonian, Serbian and Slovenian. Based on the result analysis of specific forensic parameters, it can be assumed that the most informative marker is PENTA E for population genetic analysis and forensic testing in the population of northeast Bosnia and Herzegovina. Research results fit regional STR database of this part of Europe.
机译:在波斯尼亚和黑塞哥维那东北部人口的参考样本中分析了核微卫星标记的多样性。处理了来自无关亲戚的437个样本,并显示了三个具有亲子关系的样本。该研究的检测有效性概况指出了使用PowerPlextm16试剂盒对短串联重复序列(STR)基因座进行提取,扩增和基因分型的方法的有效选择。对15个STR基因座PowerPlextm16试剂盒的等位基因变异进行遗传分析,检测到17个样品,确定为稀有等位基因变异或微变异。将样品分为7个不同基因座的15个不同等位基因变体,分别是:基因座D7S820,​​D16S539,D3S1358,D18S51,PENTA D,PENTA E和基因座vWA。亲子鉴定中突变的遗传分析确定了基因座FGA,Penta D和D3S1358中单步突变的三个例子。观察到的STR基因座的遗传分析在II型基因座D7S820中检测到基因型组合7/10 / 11.3的三个等位基因变体。在波斯尼亚和黑塞哥维那东北部人口的代表性样本中STR基因座的种群遗传分析包括应用种群内遗传多样性和种群间多样性以及种群之间的遗传分化评估测试:东北波斯尼亚和黑塞哥维那( BH)和BH一般参考,然后是克罗地亚人口,马其顿人,塞尔维亚人和斯洛文尼亚人。根据特定法医参数的结果分析,可以认为,对波斯尼亚和黑塞哥维那东北部人口进行的基因遗传和法医测试,信息最多的标记是PENTAE。研究结果符合欧洲该地区的区域STR数据库。

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