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中国白族群体常染色体插入/缺失多态性的遗传变异与法医学效能:与其他群体的系统发育分析

Genetic variation and forensic efficiency of autosomal insertion/deletion polymorphisms in Chinese Bai ethnic group: phylogenetic analysis to other populations.

作者信息

Yang Chun-Hua, Yin Cai-Yong, Shen Chun-Mei, Guo Yu-Xin, Dong Qian, Yan Jiang-Wei, Wang Hong-Dan, Zhang Yu-Dang, Meng Hao-Tian, Jin Rui, Chen Feng, Zhu Bo-Feng

机构信息

Key Laboratory of Shaanxi Province for Craniofacial Precision Medicine Research, College of Stomatology, Xi'an Jiaotong University, Xi'an, Shaanxi, P. R. China.

Clinical Research Center of Shaanxi Province for Dental and Maxillofacial Diseases, College of Stomatology, Xi'an Jiaotong University, Xi'an, Shaanxi, P. R. China.

出版信息

Oncotarget. 2017 Jun 13;8(24):39582-39591. doi: 10.18632/oncotarget.17137.

DOI:10.18632/oncotarget.17137
PMID:28465476
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5503634/
Abstract

Thirty insertion/deletion loci were utilized to study the genetic diversities of 125 bloodstain samples collected from Bai group in Yunnan Dali region, China. The observed heterozygosity and expected heterozygosity of the 30 loci ranged from 0.1520 to 0.5680, and 0.1927 to 0.4997, respectively. No deviations from Hardy-Weinberg equilibrium tests after Bonferroni correction were found at all 30 loci in Bai group. The cumulative probability of exclusion and combined discrimination power were 0.9859 and 0.9999999999887, respectively, which indicated the 30 loci could be used as complementary genetic markers for paternity testing and were qualified for personal identification in forensic cases. We found the studied Bai group had close relationships with Tibetan, Yi and Han groups from China by the population structure, principal component analysis, population differentiations, and phylogenetic reconstruction studies. Even so, for a better understanding of Bai ethnicity's genetic milieu, DNA genotyping at various genetic markers is necessary in future studies.

摘要

利用30个插入/缺失位点对采自中国云南大理地区白族的125份血迹样本的遗传多样性进行研究。这30个位点的观察杂合度和期望杂合度分别为0.1520至0.5680和0.1927至0.4997。白族的所有30个位点经Bonferroni校正后均未发现偏离哈迪-温伯格平衡检验。排除累积概率和联合鉴别力分别为0.9859和0.9999999999887,这表明这30个位点可作为亲子鉴定的补充遗传标记,有资格用于法医案件中的个人识别。通过群体结构、主成分分析、群体分化和系统发育重建研究,我们发现所研究的白族与中国的藏族、彝族和汉族群体关系密切。即便如此,为了更好地了解白族的遗传背景,未来研究有必要对各种遗传标记进行DNA基因分型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf11/5503634/74370b6d1e0a/oncotarget-08-39582-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf11/5503634/d8bcba9f1b7d/oncotarget-08-39582-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf11/5503634/07d3c7c8584b/oncotarget-08-39582-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf11/5503634/d3c719c0f8db/oncotarget-08-39582-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf11/5503634/74370b6d1e0a/oncotarget-08-39582-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf11/5503634/d8bcba9f1b7d/oncotarget-08-39582-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf11/5503634/07d3c7c8584b/oncotarget-08-39582-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf11/5503634/d3c719c0f8db/oncotarget-08-39582-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf11/5503634/74370b6d1e0a/oncotarget-08-39582-g004.jpg

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