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首页> 外文期刊>Forensic science international >Generating population data for the EMPOP database - an overview of the mtDNA sequencing and data evaluation processes considering 273 Austrian control region sequences as example.
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Generating population data for the EMPOP database - an overview of the mtDNA sequencing and data evaluation processes considering 273 Austrian control region sequences as example.

机译:为EMPOP数据库生成种群数据-以273个奥地利控制区序列为例,对mtDNA测序和数据评估过程进行了概述。

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摘要

The European DNA profiling group (EDNAP) mtDNA population database (EMPOP) is an international collaborative project between DNA laboratories performing mtDNA analysis and the DNA laboratory of the Institute of Legal Medicine (GMI) in Innsbruck, Austria. The goal is to set up a directly accessible mtDNA population database, which can be used in routine forensic casework for frequency investigations. Here we describe a safe laboratory scheme involving electronical data handling and computer-aided data transfer, which help to minimize errors originating from potential sample mix-up, data misinterpretation and incorrect transcription. The procedure is demonstrated by example of an mtDNA control region population study on 273 unrelated individuals from Austria. Our population sample was compared with five other European populations via an analysis of molecular variance (AMOVA). The inclusion of regions outside HVS-I and HVS-II increased the amount of information on the haplogroup diagnostic sites in the control region. Most of the haplotypes in Austrians fell into haplogroups H, J, K, T, and U. The random match probability in Austrians was 1:125; the average number of nucleotide differences between individuals in the Austrian database was 9.32.
机译:欧洲DNA分析组(EDNAP)mtDNA人口数据库(EMPOP)是执行mtDNA分析的DNA实验室与奥地利因斯布鲁克法律医学研究所(GMI)的DNA实验室之间的国际合作项目。目标是建立可直接访问的mtDNA种群数据库,该数据库可用于常规法医案例研究中以进行频率调查。在这里,我们描述了一种安全的实验室方案,其中涉及电子数据处理和计算机辅助数据传输,这有助于最大程度地减少由潜在的样品混淆,数据误解和错误转录引起的错误。通过对来自奥地利的273名无关个体的mtDNA控制区域人群研究的实例证明了该程序。通过分子差异分析(AMOVA),将我们的人口样本与其他五个欧洲人口进行了比较。 HVS-I和HVS-II以外区域的包含增加了控制区域中单倍群诊断位点的信息量。奥地利人中的大多数单倍型都属于H,J,K,T和U的单倍群。奥地利人中的随机匹配机率是1:125;奥地利数据库中个人之间核苷酸差异的平均数为9.32。

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