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印度中央邦比尔部落人群中Investigator Argus X STR试剂盒12个X染色体短串联重复序列(STR)位点的基因多态性研究

Genetic polymorphism study on 12 X STR loci of investigator Argus X STR kit in Bhil tribal population of Madhya Pradesh, India.

作者信息

Shrivastava Pankaj, Jain Toshi, Gupta Umang, Trivedi Veena Ben

机构信息

DNA Fingerprinting Unit, State Forensic Science Laboratory, Department of Home (Police), Govt. of Madhya Pradesh, Sagar 470001 (MP), India.

DNA Fingerprinting Unit, State Forensic Science Laboratory, Department of Home (Police), Govt. of Madhya Pradesh, Sagar 470001 (MP), India.

出版信息

Leg Med (Tokyo). 2015 May;17(3):214-7. doi: 10.1016/j.legalmed.2014.11.004. Epub 2014 Nov 28.

Abstract

The analysis of 12 X STR loci (DXS10103, DXS8378, DXS7132, DXS10134, DXS10074, DXS10101, DXS10135, DXS7423, DXS10146, DXS10079, HPRTB and DXS10148) belonging to four linkage group was done in 183 (100 males and 83 females) unrelated members of Bhil population. Heterozygosity among the studied 12 X STR loci showed a distribution of from 59.7% to 92.8%. No significant difference was recorded in the allele frequencies of males and females. The loci DXS10135 and DXS10101 were found to be most polymorphic. Haplotype diversity was found to be higher than 0.990 for all the four linkage groups. A total of 86, 69, 71 and 71 haplotypes were observed for linkage group I, II, III and IV, respectively. The results showed departure from Hardy-Weinberg equilibrium with respect to three loci DXS10079, DXS10135 and DXS10101. This is first report on these 12 X STR markers from India. All the loci in the Argus X 12 kit were fairly informative in the Bhil population and the population showed significant genetic variation with all the compared populations from other parts of the world.

摘要

对属于四个连锁群的12个X染色体短串联重复序列(DXS10103、DXS8378、DXS7132、DXS10134、DXS10074、DXS10101、DXS10135、DXS7423、DXS10146、DXS10079、HPRTB和DXS10148)进行了分析,研究对象为183名(100名男性和83名女性)比尔部落的无亲缘关系个体。在所研究的12个X染色体短串联重复序列位点中,杂合度分布在59.7%至92.8%之间。男性和女性的等位基因频率没有显著差异。发现DXS10135和DXS10101位点的多态性最高。所有四个连锁群的单倍型多样性均高于0.990。连锁群I、II、III和IV分别观察到86、69、71和71种单倍型。结果表明,DXS10079、DXS10135和DXS10101这三个位点偏离了哈迪-温伯格平衡。这是来自印度的关于这12个X染色体短串联重复序列标记的首次报告。阿格斯X 12试剂盒中的所有位点在比尔部落人群中都具有相当高的信息量,并且该人群与世界其他地区所有比较人群相比显示出显著的遗传变异。

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