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伏伊伏丁那省塞尔维亚人群中12个X染色体短串联重复序列(X-STR)基因座的遗传分析。

Genetic analysis of 12 X-STR loci in the Serbian population from Vojvodina Province.

作者信息

Veselinović Igor, Vapa Dušan, Djan Mihajla, Veličković Nevena, Veljović Tanja, Petrić Galina

机构信息

Clinical Center of Vojvodina, Medical Faculty, University of Novi Sad, Hajduk-Veljkova 1, Novi Sad, 21 000, Serbia.

Department of Biology and Ecology, Faculty of Sciences, University of Novi Sad, Trg Dositeja Obradovića 2, Novi Sad, 21 000, Serbia.

出版信息

Int J Legal Med. 2018 Mar;132(2):405-408. doi: 10.1007/s00414-017-1677-4. Epub 2017 Sep 3.

Abstract

The analysis of 12 X-STR loci included in the Investigator® Argus X-12 kit was performed on a sample of 325 unrelated persons from Vojvodina Province, Republic of Serbia. No significant differences were observed in the allele frequencies in males and females. Heterozygosity values among the studied loci ranged from 67.62 to 94.28%. All loci in female individuals were consistent with the Hardy-Weinberg equilibrium test. The combined power of discrimination values in male and female individuals was 0.9999999994 and 0.999999999999999, respectively. The combined mean exclusion chance was 0.999998 in deficiency cases, 0.9999999977 in normal trio cases, and 0.9999994 in duo cases. Loci DXS10135 and DXS10101 were found to be most polymorphic. The haplotype diversity was found to be greater than 0.993 for all linkage groups. The exact test for pairwise linkage disequilibrium for the 12 loci in the male samples showed significant linkage disequilibrium for the DXS10103-DXS10101 and DXS10134-DXS10146 pairs of loci. The results from the current study confirmed that the panel of 12 X-STR loci is highly polymorphic and informative and can be implemented as a powerful tool in deficient paternity testing and kinship analysis, as well as a useful complement tool of autosomal short tandem repeats (STRs) in forensic investigation. Population differentiation analyses indicated significant differences in genetic structure between the Serbian population and the geographically and ethno-linguistically distant populations, while genetic homogeneity was present in populations with similar geographic origin.

摘要

对塞尔维亚共和国伏伊伏丁那省325名无关个体的样本进行了Investigator® Argus X-12试剂盒中包含的12个X-STR基因座的分析。在男性和女性的等位基因频率上未观察到显著差异。所研究基因座的杂合度值范围为67.62%至94.28%。女性个体中的所有基因座均符合哈迪-温伯格平衡检验。男性和女性个体的联合鉴别力值分别为0.9999999994和0.999999999999999。在缺失案例中,联合平均排除机会为0.999998,在正常三联体案例中为0.9999999977,在二联体案例中为0.9999994。发现基因座DXS10135和DXS10101具有最高的多态性。所有连锁群的单倍型多样性均大于0.993。对男性样本中12个基因座进行的成对连锁不平衡精确检验显示,基因座对DXS10103-DXS10101和DXS10134-DXS10146存在显著的连锁不平衡。本研究结果证实,12个X-STR基因座组合具有高度多态性和信息性,可作为缺失父权检测和亲属关系分析的有力工具,以及法医调查中常染色体短串联重复序列(STR)的有用补充工具。群体分化分析表明,塞尔维亚人群与地理和民族语言上遥远的人群之间在遗传结构上存在显著差异,而地理起源相似的人群中存在遗传同质性。

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