首页> 中文期刊>法医学杂志 >江苏汉族人群30个插入/缺失位点的遗传多态性

江苏汉族人群30个插入/缺失位点的遗传多态性

     

摘要

Objective To investigate the genetic information of 30 insertion/deletion (InDel) loci in Han population from Jiangsu Province, and to explore the application values of Investigator? DIPplex kit for guiding the forensic analysis in Han population from Jiangsu Province. Methods The autosomal InDel loci of 305 unrelated healthy Han individuals from Jiangsu Province were genotyped and analysed by In-vestigator? DIPplex kit, and the allelic frequencies and forensic parameters of 30 InDel loci were statis-tically analysed. Results The distribution of 30 InDel loci in Han population from Jiangsu Province con-formed to Hardy-Weinberg equilibrium. The minor allele frequencies of 21 InDel loci were above 0.3. The polymorphism information content ranged from 0.089 to 0.375, while the discrimination power dis-tributed from 0.093 to 0.500. The paternity exclusion in duo cases and trio cases were 0.047-0.250 and 0.046-0.219, respectively. The linkage disequilibrium analysis of 30 InDel loci showed that all loci were independent from each other. The combined discrimination power was 1-7.369 ×10-8, whereas the com-bined mean exclusion chance in duo cases was 0.998933978, in trio cases was 0.997806392. The Fst values were all less than 0.06 except HLD118 and other four loci, which showed small differences be-tween groups. Conclusion The InDel loci of Investigator ? DIPplex kit can be used as complementary genetic markers for the cases associated with forensic genetics.%目的 调查30个插入/缺失(insertion/deletion,InDel)位点在江苏汉族人群中的遗传学信息,评估Investigator?DIPplex试剂盒的使用价值,并用于指导江苏汉族人群的法医学分析.方法 用Investigator?DIPplex试剂盒对江苏地区305名汉族健康无关个体进行常染色体InDel位点的分型检测,统计分析30个InDel位点的频率数据及遗传学参数.结果 30个InDel位点在江苏汉族人群中的分布均符合Hardy-Wein-berg平衡,有21个InDel位点的最小等位基因频率大于0.3.多态信息含量为0.089~0.375,个体识别率为0.093~0.500,二联体非父排除率为0.047~0.250,三联体非父排除率为0.046~0.219.30个InDel位点经连锁不平衡分析,各位点之间相互独立,累积个体识别率为1-7.369×10-8,二联体累积非父排除率为0.998933978,三联体累积非父排除率为0.997806392.除HLD118等5个位点外,群体间Fst值均小于0.06,在群体间差异较小.结论 Investigator?DIPplex试剂盒中所含有的InDel位点可作为补充遗传标记应用于法医物证学相关检案工作.

著录项

相似文献

  • 中文文献
  • 外文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号