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      Genetic variation and phylogenetic analysis of 23 STR in Chinese Han population from Hainan, Southern China

      research-article
      , PhD a , , PhD b , c , , MD a , , MD a , , PhD a , , PhD a , * ,
      Medicine
      Lippincott Williams & Wilkins
      forensic genetics, genetic polymorphism, Hainan Han, STR

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          Abstract

          The forensic characteristics and genetic relationships of Hainan Han population are still not fully understood. The aim of this study was to investigate the forensic features and genetic variations of 23 short tandem repeat (STR) included in the Huaxia TM Platinum system in Hainan Han and analyze the population genetic relationships between Hainan Han and other adjacent Chinese populations. The genetic polymorphisms of 23 STR loci included in the Huaxia TM Platinum kit were evaluated from 2971 Hainan Han individuals. Comprehensive comparisons were conducted based on genetic distance, phylogenetic tree, multidimensional scaling and principal component analysis (PCA) to explore inter-population genetic relationship. The combined power of discrimination (CPD) and the combined power of exclusion (CPE) of the 23 STR loci was 0.999 999 999 999 999 999 999 999 999 819 and 0.999 999 999 625 408, respectively. The investigated Hainan Han population has high genetic similarity with geographically close Han populations, while great genetic difference with other ethnic minorities, prominently in Yunnan Miao, Xinjiang Uygurs, Xinjiang Kazakh, and Tibetans. Our study found the 23 STR loci were highly polymorphic and suitable for forensic personal identification and paternity testing in Hainan Han population. Genetic similarity widely existed among Han populations from different regions, and significant genetic divergence existed between Han populations and some ethnic minorities. The populations genetic diversity and similarity were closely associated with ethnic origin and geographical distribution.

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          Most cited references27

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          MEGA7: Molecular Evolutionary Genetics Analysis Version 7.0 for Bigger Datasets.

          We present the latest version of the Molecular Evolutionary Genetics Analysis (Mega) software, which contains many sophisticated methods and tools for phylogenomics and phylomedicine. In this major upgrade, Mega has been optimized for use on 64-bit computing systems for analyzing larger datasets. Researchers can now explore and analyze tens of thousands of sequences in Mega The new version also provides an advanced wizard for building timetrees and includes a new functionality to automatically predict gene duplication events in gene family trees. The 64-bit Mega is made available in two interfaces: graphical and command line. The graphical user interface (GUI) is a native Microsoft Windows application that can also be used on Mac OS X. The command line Mega is available as native applications for Windows, Linux, and Mac OS X. They are intended for use in high-throughput and scripted analysis. Both versions are available from www.megasoftware.net free of charge.
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            Arlequin suite ver 3.5: a new series of programs to perform population genetics analyses under Linux and Windows.

            We present here a new version of the Arlequin program available under three different forms: a Windows graphical version (Winarl35), a console version of Arlequin (arlecore), and a specific console version to compute summary statistics (arlsumstat). The command-line versions run under both Linux and Windows. The main innovations of the new version include enhanced outputs in XML format, the possibility to embed graphics displaying computation results directly into output files, and the implementation of a new method to detect loci under selection from genome scans. Command-line versions are designed to handle large series of files, and arlsumstat can be used to generate summary statistics from simulated data sets within an Approximate Bayesian Computation framework. © 2010 Blackwell Publishing Ltd.
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              Chelex 100 as a medium for simple extraction of DNA for PCR-based typing from forensic material.

              Procedures utilizing Chelex 100 chelating resin have been developed for extracting DNA from forensic-type samples for use with the PCR. The procedures are simple, rapid, involve no organic solvents and do not require multiple tube transfers for most types of samples. The extraction of DNA from semen and very small bloodstains using Chelex 100 is as efficient or more efficient than using proteinase K and phenol-chloroform extraction. DNA extracted from bloodstains seems less prone to contain PCR inhibitors when prepared by this method. The Chelex method has been used with amplification and typing at the HLA DQ alpha locus to obtain the DQ alpha genotypes of many different types of samples, including whole blood, bloodstains, seminal stains, buccal swabs, hair and post-coital samples. The results of a concordance study are presented in which the DQ alpha genotypes of 84 samples prepared using Chelex or using conventional phenol-chloroform extraction are compared. The genotypes obtained using the two different extraction methods were identical for all samples tested.
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                Author and article information

                Contributors
                Journal
                Medicine (Baltimore)
                Medicine (Baltimore)
                MD
                Medicine
                Lippincott Williams & Wilkins (Hagerstown, MD )
                0025-7974
                1536-5964
                31 May 2024
                31 May 2024
                : 103
                : 22
                : e38428
                Affiliations
                [a ]Department of Forensic Medicine, Hainan Provincial Academician Workstation (Tropical Forensic Medicine), Hainan Province Tropical Forensic Engineering Research Center, Hainan Medical University, Haikou, China
                [b ]Department of Pathology, School of Basic Medicine and Life Sciences, Hainan Medical University, Haikou, China
                [c ]Department of Pathology, The First Affiliated Hospital of Hainan Medical University, Haikou, China.
                Author notes
                [* ]Correspondence: Peng Zhang, Department of Forensic Medicine, Hainan Provincial Academician Workstation (Tropical Forensic Medicine), Hainan Province Tropical Forensic Engineering Research Center, Hainan Medical University, Haikou 571199, Xueyuan Road 3#, Longhua District, China (e-mail: 972421821@ 123456qq.com ).
                Author information
                https://orcid.org/0000-0001-8836-1668
                Article
                MD-D-23-11548 00019
                10.1097/MD.0000000000038428
                11142786
                24813949-2fff-47f0-9ea0-33a27a0f91c9
                Copyright © 2024 the Author(s). Published by Wolters Kluwer Health, Inc.

                This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 22 December 2023
                : 01 March 2024
                : 10 May 2024
                Categories
                4700
                Research Article
                Observational Study
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                forensic genetics,genetic polymorphism,hainan han,str
                forensic genetics, genetic polymorphism, hainan han, str

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