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首页> 外文期刊>Molecular and Cellular Probes: The Location, Diagnosis and Monitoring of Disease by Specific Molecules and Cell Lines >Allele frequency distributions at several variable number of tandem repeat (VNTR) and short tandem repeat (STR) loci in a restricted Caucasian population from south Italy and their evaluation for paternity and forensic use.
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Allele frequency distributions at several variable number of tandem repeat (VNTR) and short tandem repeat (STR) loci in a restricted Caucasian population from south Italy and their evaluation for paternity and forensic use.

机译:来自意大利南部的受限制的白种人人群中几个可变数目的串联重复序列(VNTR)和短串联重复序列(STR)位点的等位基因频率分布及其对亲子鉴定和法医使用的评估。

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摘要

Allele frequencies at six VNTR loci, 11 STR loci, and at the HLA-DQA1 locus were evaluated in a well-defined population from Campania (South Italy). The allele frequencies of three VNTR loci, 11 STR loci, and the HLA-DQA1 locus were compared with data obtained from a general Caucasian reference population in the USA. The aim of this study was to determine the power of each single locus and group of loci for forensic and paternity testing purposes. Significant differences between the allele frequencies of the two populations were found in two VNTR loci, four STR loci and in the HLA-DQA1 locus. The two populations were in Hardy-Weinberg equilibrium for the STR loci, but as expected, not for some VNTR loci. It was also found that: (i) the discriminatory power of two STR systems (nine and 11 loci, respectively) is similar in the two populations analysed; and (ii) that the allele frequencies for the STR systems of a large reference population can always be applied to subjects of a small subpopulation. In conclusion, for forensic purposes and for paternity testing, most of the 11 STR loci examined can be analysed using allele frequencies from a general Caucasian reference population without typing subpopulations, whereas the VNTR loci must be subtyped.
机译:在来自坎帕尼亚(意大利南部)的明确人群中,评估了六个VNTR基因座,11个STR基因座以及HLA-DQA1基因座的等位基因频率。将三个VNTR基因座,11个STR基因座和HLA-DQA1基因座的等位基因频率与从美国普通白种人参考人群获得的数据进行了比较。这项研究的目的是确定法医和亲子鉴定目的每个基因座和基因座组的功能。在两个VNTR基因座,四个STR基因座和HLA-DQA1基因座中发现了两个种群的等位基因频率之间的显着差异。对于STR基因座,两个种群处于Hardy-Weinberg平衡状态,但正如预期的那样,对于某些VNTR基因座而言,并非如此。还发现:(i)在所分析的两个种群中,两个STR系统(分别为9个和11个基因座)的区分能力相似; (ii)大参考人群的STR系统的等位基因频率始终可以应用于小亚群的受试者。总之,出于司法鉴定和亲子鉴定的目的,可以使用来自普通白种人参考人群的等位基因频率分析所检查的11个STR基因座中的大多数,而无需键入亚群,而VNTR基因座必须进行亚型分析。

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