Genetic polymorphism of the 26 short tandem repeat loci in the Chinese Hebei Han population using two commercial forensic kits

被引:7
作者
Lei, Liang [1 ]
Xu, Jie [1 ]
Du, Qingqing [1 ]
Fu, Lihong [1 ]
Zhang, Xiaojing [1 ]
Yu, Feng [1 ]
Ma, Chunling [1 ]
Cong, Bin [1 ]
Li, Shujin [1 ]
机构
[1] Hebei Med Univ, Dept Forens Med, Hebei Key Lab Forens Med, Shijiazhuang 050017, Hebei, Peoples R China
基金
中国国家自然科学基金;
关键词
Autosomal DNA marker; Short tandem repeat; Population genetics; Linkage disequilibrium; Han population; 15 STR LOCI; ETHNIC-MINORITY GROUP; ALLELE FREQUENCIES; D10S2325; SAMPLE; POLAND;
D O I
10.1007/s11033-014-3761-x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We determined the allele frequencies and forensic parameters for the 26 short tandem repeat (STR) autosomal markers in two commercial kits (the Investigator HDplex and AmpFLSTR (R) Identifiler (R) systems) for 183 unrelated individuals from the Han population of the Hebei Province of China. The 26 STRs were all in Hardy-Weinberg equilibrium. No linkage disequilibrium was detected between any pair of loci. The combined power of discrimination and the combined power of exclusion for the 26 STR loci were 1-7.74E-31 and 1-1.21E-11, respectively. Six rare alleles of D10S2325 were identified and named 20, 21, 22, 23, 24, and 31. All the length of the six rare alleles were out of the range of allelic ladder. We calculated the population pairwise genetic distance based on the allele frequencies, using published population data including German, central Polish, south Dutch, northeastern Polish, south Brazilian, Korean, Sichuan Han of China, and Shanghai Han of China. Also we examined the population pairwise genetic distance of loci included in Identifiler system between Hebei Han and other ethnic population of China. These 26 autosomal STR loci could provide highly informative polymorphic data for paternity testing and forensic identification in the Hebei Han population in China. Because they are all in linkage equilibrium, they could be used together to solve deficient kinship cases or cases with mutations.
引用
收藏
页码:217 / 225
页数:9
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