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短串联重复序列多态性分析作为了解关中汉族人群遗传特征的基础。

The Polymorphism Analyses of Short Tandem Repeats as a Basis for Understanding the Genetic Characteristics of the Guanzhong Han Population.

机构信息

Multi-Omics Innovative Research Center of Forensic Identification; Department of Forensic Genetics, School of Forensic Medicine, Southern Medical University, Guangzhou 510515, China.

Key Laboratory of Shaanxi Province for Craniofacial Precision Medicine Research, College of Stomatology, Xi'an Jiaotong University, Xi'an 710004, China.

出版信息

Biomed Res Int. 2021 Feb 25;2021:8887244. doi: 10.1155/2021/8887244. eCollection 2021.

DOI:10.1155/2021/8887244
PMID:33728348
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7936557/
Abstract

The short tandem repeat (STR) loci are polymorphic markers in the combined DNA index system (CODIS) and non-CODIS STR loci. Due to the highly polymorphic characteristic of STR loci, they are popular and widely used in forensic DNA typing laboratories. In this study, 22 STR loci (1 CODIS, 21 non-CODIS STR loci) and an Amelogenin locus were genotyped and analyzed in 590 unrelated individuals of the Guanzhong Han population. None of the 22 STR loci deviated from the Hardy-Weinberg equilibrium, and all the loci were in the linkage equilibrium state. We observed 247 alleles, and the corresponding allelic frequencies ranged from 0.0008 to 0.3695 in the Guanzhong Han population. The combined power of discrimination and the cumulative exclusion probability was 0.999 999 999 999 999 999 999 999 999 346 36 and 0.999 999 999 709 74, respectively. The results including Nei's genetic distance, multidimensional scaling analysis, and principal component analysis showed that the Guanzhong Han population has closer genetic affinities with Northern Han, Chengdu Han, and Xinjiang Hui groups from China based on allelic frequencies of 15 overlapped STR loci from Guanzhong Han and 13 reference groups. The present results indicated that Microreader™ 23sp ID kit included highly polymorphic loci, and it could be well used for individual identification, paternity testing, and population genetics in the Guanzhong Han population.

摘要

短串联重复(STR)基因座是联合 DNA 索引系统(CODIS)和非 CODIS STR 基因座中的多态性标记。由于 STR 基因座具有高度多态性的特点,它们在法医 DNA 分型实验室中得到了广泛的应用。本研究在 590 名无关的关中汉族个体中对 22 个 STR 基因座(1 个 CODIS,21 个非 CODIS STR 基因座)和一个 Amelogenin 基因座进行了基因分型和分析。22 个 STR 基因座均未偏离 Hardy-Weinberg 平衡,所有基因座均处于连锁平衡状态。我们观察到 247 个等位基因,对应的等位基因频率在关中汉族人群中范围为 0.0008 至 0.3695。联合鉴别力和累积排除概率分别为 0.999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999999

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8937/7936557/47e3aab68fb7/BMRI2021-8887244.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8937/7936557/dff32382e6bb/BMRI2021-8887244.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8937/7936557/046bcc474b66/BMRI2021-8887244.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8937/7936557/70009c6bd42c/BMRI2021-8887244.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8937/7936557/0f7d5827ef90/BMRI2021-8887244.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8937/7936557/47e3aab68fb7/BMRI2021-8887244.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8937/7936557/dff32382e6bb/BMRI2021-8887244.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8937/7936557/046bcc474b66/BMRI2021-8887244.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8937/7936557/70009c6bd42c/BMRI2021-8887244.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8937/7936557/0f7d5827ef90/BMRI2021-8887244.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8937/7936557/47e3aab68fb7/BMRI2021-8887244.005.jpg

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