Investigator® 24plex GO!试剂盒评估及南非四个人群的相关等位基因频率数据

Q3 Medicine
Laura Jane Heathfield , Lorraine Nel, Kate Megan Reid
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引用次数: 0

摘要

在这项研究中,使用 Investigator® 24plex GO!Kit (QIAGEN, Hilden, Germany)生成了南非人的人口数据。参与者代表了南非的四大人口群体,自报祖籍分别为非洲人(n = 208)、欧洲人(n = 213)、印度人/亚洲人(n = 103)或混血人(n = 209)。使用 Arlequin(v.3.5.2.2)和 FORSTAT(v1.0)计算了每个人群的等位基因频率数据和法证参数。在所有人群中,TPOX 的鉴别能力最低,但在非洲人群中,THO1 的鉴别能力最低。在所有人群中,SE33 的区分能力最高(0.98),在 Admixed 人群中观察到 38 种不同的等位基因。使用 ForenSeq™ DNA Signature Prep 试剂盒对显示出新等位基因或异常的样本进行了大规模平行测序,确认了以下结果:一个 Amelogenin 的 Y 等位基因为空、十个 TPOX 三平行现象和四个新的微变异等位基因。在 SE33 中还观察到另外四个新型等位基因,但由于 SE33 不在 ForenSeq™ DNA Signature Prep 套件中,因此仍未得到证实。此外,有 9 个个体在 D1S1656 上存在等位基因 8 或 9,这些等位基因的峰值出现在电泳图上 D1S1656 标记范围之前,并在 DYS391 标记内显示为一个峰值。虽然这种现象在总体上很少见(1.2%),但这 9 个个体来自 4 个群体中的 3 个群体,这促使我们调整 Investigator® 24plex PCR 化学方法,以避免 D1S1656 与 DYS391 的等位基因重叠。总之,这些发现凸显了南非人口遗传构成的多样性,并强调了当地人口研究的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of the Investigator® 24plex GO! kit and associated allele frequency data for four South African population groups

In this study, population data were generated from South Africans using the Investigator® 24plex GO! Kit (QIAGEN, Hilden, Germany). Participants represented the four major population groups in South Africa, with self-reported ancestral origin being African (n = 208), European (n = 213), Indian/Asian (n = 103) or Admixed (n = 209). Allele frequency data and forensic parameters were calculated for each population group using Arlequin (v.3.5.2.2) and FORSTAT (v1.0). TPOX had the lowest discrimination capacity for all population groups, except for the African population group where THO1 was the least informative. SE33 had the highest discrimination capacity for all population groups (>0.98), with 38 different alleles observed in the Admixed population group. Samples exhibiting novel alleles or anomalies underwent massively parallel sequencing using the ForenSeq™ DNA Signature Prep kit, which confirmed the following results: one null Y allele at Amelogenin, ten instances of TPOX tri-allelism and four novel micro-variant alleles. An additional four novel alleles in SE33 were observed but remain unconfirmed, due to SE33 not being included in the ForenSeq™ DNA Signature Prep kit. Moreover, nine individuals had an allele 8 or 9 at D1S1656, where the peaks for these alleles occur before the D1S1656 marker range on the electropherogram and showed as a peak within the DYS391 marker. Although this observation was rare overall (1.2%), these nine individuals were from three of the four population groups, which motivates for the adjustment of the Investigator® 24plex PCR chemistry to avoid allelic overlap of D1S1656 with DYS391. Overall, these findings highlight the diverse genetic makeup of the South Africa population and accentuate the importance of local population studies.

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来源期刊
Forensic Science International: Reports
Forensic Science International: Reports Medicine-Pathology and Forensic Medicine
CiteScore
2.40
自引率
0.00%
发文量
47
审稿时长
57 days
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