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Genetic polymorphisms of twelve X-STRs of the investigator Argus X-l 2 kit and additional six X-STR centromere region loci in an Egyptian population sample

机译:埃及人口样本中研究者Argus X-12试剂盒的12个X-STR和另外6个X-STR着丝粒区域基因座的遗传多态性

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Recently, many researchers have focused on analysis of different X-chromosomal STRs as they bear the potential to efficiently complement the analysis of autosomal and Y-chromosomal STRs in solving special complex kinship deficiency cases. In the current study we examined a sample of 250 unrelated Egyptian males with the Investigator Argus X-l 2 kit (Qiagen GmbH, Hilden, Germany) which detects 12 X-STR markers distributed over the entire X-chromosome as four closely linked clusters. Microvariant off ladder alleles as well as null alleles have been detected in some loci. Furthermore, discordant results were observed between the Investigator Argus X-l 2 and the Mentype? Argus X-8 kits (Biotype AG, Dresden, Germany). New primers were designed for loci DXS10101, DXS10146 and DXS10148 to correct the allele drop outs observed in these loci with the Investigator Argus X-l 2 kit. Additionally, DNA sequence analysis revealed the polymorphisms responsible for the allele drop outs. Furthermore, six additional X-STRs (DXS10161, DXS10159, DXS10162, DXS10163, DXS10164 and DXS10165) located in the centromere region at Xpll.21-Xqll.l were examined in a single multiplex reaction. Allele and haplotype frequencies as well as different forensic statistical parameters of the 18 X-STR loci tested indicated that they are highly informative in different forensic applications in the Egyptian population. However, some modifications still need to be performed on the Investigator Argus X-l 2 kit before its use in forensic casework is validated.
机译:近来,许多研究者将重点放在对不同X染色体STR的分析上,因为它们有潜力在解决特殊的复杂亲缘关系不足的情况下有效补充常染色体和Y染色体STR的分析。在当前的研究中,我们使用研究者Argus X-1 2试剂盒(Qiagen GmbH,希尔登,德国)检查了250名无亲缘关系的埃及男性样本,该试剂盒检测到12个X-STR标记以四个紧密连接的簇分布在整个X染色体上。在某些基因座中已检测到梯形等位基因等位基因以及无效等位基因。此外,在研究者Argus X-12和Mentype?之间观察到不一致的结果。 Argus X-8套件(Biotype AG,德累斯顿,德国)。设计了针对基因座DXS10101,DXS10146和DXS10148的新引物,以使用Investigator Argus X-12试剂盒纠正在这些基因座中观察到的等位基因缺失。此外,DNA序列分析揭示了导致等位基因缺失的多态性。此外,在单个多重反应中检查了位于Xpll.21-Xqll.1着丝粒区域的六个另外的X-STR(DXS10161,DXS10159,DXS10162,DXS10163,DXS10164和DXS10165)。测试的18个X-STR基因座的等位基因和单倍型频率以及不同的法医统计参数表明,它们在埃及人群的不同法医应用中具有很高的信息价值。但是,在验证其在法医案件中的用途之前,仍需要对Investigator Argus X-1 2套件进行一些修改。

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