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首页> 外文期刊>Forensic science international. Genetics >Indel markers: Genetic diversity of 38 polymorphisms in Brazilian populations and application in a paternity investigation with post mortem material
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Indel markers: Genetic diversity of 38 polymorphisms in Brazilian populations and application in a paternity investigation with post mortem material

机译:Indel标记:巴西人群中38个多态性的遗传多样性及其在验尸资料中进行亲子鉴定的应用

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摘要

Aiming to evaluate the usefulness of 38 non-coding bi-allelic autosomal indels in genetic identification and kinship testing, three Brazilian population samples were studied: two from Rio de Janeiro (including a sample of individuals with self-declared African ancestry) and one Native American population of Terena from Mato Grosso do Sul. Based on the observed allele frequencies, parameters of forensic relevance were calculated. The combined power of discrimination of the 38 indels was high in all studied groups (PD ≥ 0.9999999999997), although slightly lower in Native Americans. Genetic distance analysis showed significant differences between the allele frequencies in the Rio de Janeiro population and those previously reported for Europeans, Africans and Asians explained by its intermediate position between Europeans and Africans. As expected, the Terena sample was significantly different from all the other populations: Brazilians from Rio de Janeiro general population and with self-declared African ancestry, Europeans, Africans and East Asians. Finally, the performance of the 38-indel multiplex assay was tested in post-mortem material with positive results, supporting the use of short amplicon bi-allelic markers as an additional tool to STR analysis when DNA molecules are degraded.
机译:为了评估38个非编码双等位基因常染色体indel在遗传鉴定和亲缘关系测试中的有用性,研究了三个巴西人口样本:两个来自里约热内卢(包括自称非洲血统的个体)和一个土著来自南马托格罗索州的Terena美国人口。根据观察到的等位基因频率,计算法医相关参数。在所有研究组中,对38个indel的综合辨别力较高(PD≥0.9999999999997),尽管在美洲印第安人中略低。遗传距离分析显示,里约热内卢人口的等位基因频率与先前报道的欧洲人,非洲人和亚洲人的等位基因频率之间存在显着差异,这是由于其在欧洲人和非洲人之间的中间位置所致。不出所料,特雷纳(Terena)的样本与所有其他人口有显着差异:来自里约热内卢总人口,自称具有非洲血统的巴西人,欧洲人,非洲人和东亚人。最后,在验尸材料中测试了38插入缺失多重分析的性能,并获得了积极的结果,支持在DNA分子降解时,使用短扩增子双等位基因标记作为STR分析的附加工具。

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