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瑞士西南部人群中线粒体DNA的法医鉴定。

Forensic evaluation of mtDNA in a population from south west Switzerland.

作者信息

Dimo-Simonin N, Grange F, Taroni F, Brandt-Casadevall C, Mangin P

机构信息

Institute Universitaire de Médecine Légale, Lausanne, Switzerland.

出版信息

Int J Legal Med. 2000;113(2):89-97. doi: 10.1007/pl00007715.

Abstract

The polymorphism of the two hypervariable segments (HVI and HVII) of the control region of mtDNA was analyzed in a population of 154 unrelated individuals from south west Switzerland using a fluorescent based capillary electrophoresis sequencing method. In our population data of 154 random individuals, 137 mtDNA types were observed. Of these, 124 sequences were observed only in one individual whereas 10 sequences were observed in 2 individuals, 2 sequences in 3 individuals and 1 sequence in 4 individuals. The probability of two unrelated individuals having the same sequence was 0.84%. The results were compared with four other Caucasian populations. Furthermore, the usefulness of the mtDNA sequencing was tested, for exclusion and inclusion, in 18 forensic cases including 69 evidence samples and 44 reference samples. Despite the fact that 55% of the evidence samples yielded a negative result for the nuclear DNA with the human dot quantitation system, the success rate of the mtDNA sequencing was 71.0%. This validation study proves the great usefulness and sensitivity of the mtDNA sequencing technique using nested PCR and fluorescent capillary electrophoresis.

摘要

采用基于荧光的毛细管电泳测序方法,对来自瑞士西南部的154名无血缘关系个体的群体进行了线粒体DNA(mtDNA)控制区两个高变区(HVI和HVII)多态性分析。在我们154名随机个体的群体数据中,观察到137种mtDNA类型。其中,124个序列仅在1个个体中观察到,10个序列在2个个体中观察到,2个序列在3个个体中观察到,1个序列在4个个体中观察到。两个无血缘关系个体具有相同序列的概率为0.84%。将结果与其他四个高加索人群体进行了比较。此外,还在18起法医案件中测试了mtDNA测序在排除和认定方面的实用性,这些案件包括69个证据样本和44个参考样本。尽管使用人类点定量系统对55%的证据样本进行核DNA检测结果为阴性,但mtDNA测序的成功率为71.0%。这项验证研究证明了使用巢式PCR和荧光毛细管电泳的mtDNA测序技术具有很大的实用性和敏感性。

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