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首页> 外文期刊>International journal of legal medicine >Development of the nine X-STR loci typing system and genetic analysis in three nationality populations from China.
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Development of the nine X-STR loci typing system and genetic analysis in three nationality populations from China.

机译:在中国的三个民族中开发了九个X-STR基因座分型系统并进行了遗传分析。

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This study is to develop a new multiplex polymerase chain reaction (PCR) system that simultaneously amplifies the nine X-chromosome short tandem repeats loci in the same PCR reaction, and to explore their polymorphism and mutation rate among three nationality populations from China. These loci included DXS6854, DXS9902, DXS6809, GATA172D05, HPRTB, DXS7423, DXS6807, DXS8378, and DXS8377. The samples of 890 (484 males and 406 females) unrelated individuals from Guangdong Han population, Xinjiang Uigur, and Inner-Mongolia Mongol were successfully analyzed using this multiplex system. The allele frequencies and mutation rates of the nine loci were investigated, and the comparison of allele frequency distribution among different populations was performed. There were 87 alleles for all the loci, and six to 18 alleles for each locus observed by our new multiplex PCR system. Polymorphism information content was 0.4998-0.9101, and power of discrimination in females was 0.6518-0.9846. Five cases with mutation of above loci were detected in 5,310 meioses. Pair-wise comparisons of allele frequencies distribution showed significant differences for most loci among different populations. Our results indicate that this multiplex system is very useful for identification analysis, and that the information about polymorphism and mutation rate is necessary for forensic application in three nationality populations from China.
机译:这项研究旨在开发一种新的多重聚合酶链反应(PCR)系统,该系统在同一PCR反应中同时扩增9个X染色体短串联重复序列基因座,并探讨它们在中国3个民族中的多态性和突变率。这些基因座包括DXS6854,DXS9902,DXS6809,GATA172D05,HPRTB,DXS7423,DXS6807,DXS8378和DXS8377。使用该多重系统成功地分析了来自广东汉族人群,新疆维吾尔族和内蒙古蒙古族的890名(484名男性和406名女性)无关个体的样本。研究了这9个基因座的等位基因频率和突变率,并比较了不同人群之间的等位基因频率分布。通过我们的新的多重PCR系统,观察到所有基因座有87个等位基因,每个基因座有6至18个等位基因。多态性信息含量为0.4998-0.9101,女性的辨别力为0.6518-0.9846。在5,310个基因中检测到5个以上基因座突变的病例。等位基因频率分布的成对比较显示了不同人群之间大多数基因座的显着差异。我们的结果表明,该多路复用系统对于鉴定分析非常有用,并且有关多态性和突变率的信息对于在中国的三个民族人群中进行法医学应用是必不可少的。

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