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使用Investigator(®) DIPplex对中国西南、南方和西北人群进行插入/缺失多态性的比较研究。

A comparative study of insertion/deletion polymorphisms applied among Southwest, South and Northwest Chinese populations using Investigator(®) DIPplex.

作者信息

Wang Li, Lv Meili, Zaumsegel Daniel, Zhang Lushun, Liu Fengji, Xiang Jihua, Li Jun, Schneider Peter M, Liang Weibo, Zhang Lin

机构信息

Institute of Forensic Medicine, West China School of Basic Science and Forensic Medicine, Sichuan University, Chengdu, PR China.

Institute of Legal Medicine, Faculty of Medicine, University of Cologne, Cologne, Germany.

出版信息

Forensic Sci Int Genet. 2016 Mar;21:10-4. doi: 10.1016/j.fsigen.2015.08.005. Epub 2015 Aug 21.

Abstract

The low mutation rates, short amplicon sizes and length variation characteristics of biallelic insertion/deletion polymorphisms (INDELs) are features that allow combining advantages of both STR and SNP markers for genetic analysis. The Qiagen Investigator DIPplex kit contains 30 biallelic autosomal INDELs plus Amelogenin for forensic personal identification and parentage testing. This study compares general performances, forensic and population data collected in 7 Chinese ethnic populations (Han, Tibetan, Yi, Zhuang, Dong, Miao and Uyghur) from three areas (Southwest, South and Northwest) of China by DIPplex kit. There were no significant departures from Hardy-Weinberg equilibrium (HWE) of the 30 markers in all the tested populations after Bonferroni correction. The combined matching probabilities ranged from 1.4273×10(-10) for the Dong minority to 1.2817×10(-12) for the Uyghur minority. The combined power of paternity exclusion was from 0.9854 to 0.9968. All pairwise genetic differences (FST) between the seven ethnic groups were less than 0.05, and the results of STRUCTURE analysis did not indicate the presence of substructures suggesting genetic similarity among the populations in these three areas. The DIPplex kit can be used as a good additional tool for forensic personal identification in these three areas of China.

摘要

双等位基因插入/缺失多态性(INDEL)的低突变率、短扩增子大小和长度变异特征,使其兼具STR和SNP标记的优势,适用于遗传分析。Qiagen Investigator DIPplex试剂盒包含30个双等位基因常染色体INDEL以及用于法医个人识别和亲权鉴定的牙釉蛋白。本研究比较了DIPplex试剂盒在中国三个地区(西南、南部和西北)的7个中国民族群体(汉族、藏族、彝族、壮族、侗族、苗族和维吾尔族)中收集的一般性能、法医和群体数据。经Bonferroni校正后,所有测试群体中30个标记均未显著偏离哈迪-温伯格平衡(HWE)。联合匹配概率范围从侗族的1.4273×10(-10)到维吾尔族的1.2817×10(-12)。联合亲权排除率为0.9854至0.9968。七个民族群体之间的所有成对遗传差异(FST)均小于0.05,STRUCTURE分析结果未表明存在亚结构,这表明这三个地区的群体之间具有遗传相似性。DIPplex试剂盒可作为中国这三个地区法医个人识别的良好补充工具。

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