用于接触DNA分析的20个CODIS核心STR位点的评价

V. Saamia, A. Yudianto, M. Nurjayadi, Novitasari Novitasari, A. Furqoni, Racy Youngest, Ajeng Tiara Parji Saputri, Ade Maysaroh, Riski Suranto
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引用次数: 0

摘要

DNA谱是STR等位基因位点的组合,是模板DNA扩增的结果。联邦调查局已经确定了20个核心STR基因座,用于法医案件中的人类鉴定。本研究的目的是评估20个CODIS核心STR位点,作为DNA触摸检查的参考。9名捐赠者分别有高、中、低三种脱毛状态,他们拿着样品,同时系上两种类型的绳子,多孔和无孔。然后,对每根绳子使用两种技术对触摸样本进行采样:双重拭子和胶带提升。提取DNA并采用实时荧光定量PCR技术测定每个处理获得的DNA浓度。扩增24个STR基因座,并进行毛细管电泳分析。选择两个PCR循环来确定添加周期对未成功扩增的DNA浓度的影响。本研究结果表明,触摸DNA的数量对STR扩增成功率的影响较大。20个STR CODIS位点的等位基因在接触DNA浓度低于0.0625 ng/µl时均无法扩增。结果表明,每个位点上的靶等位基因越长,越容易发生等位基因脱落。然而,用于DNA检测的最佳STR位点长度小于200个核苷酸。
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 20 CODIS Core STR Loci For Touch DNA Analysis
The DNA profile is a combination of STR alleles loci as a result of template DNA amplification. The FBI has defined 20 core STR loci for human identification in forensic cases. The aim of this study was to evaluate the twenty CODIS core STR loci to be a reference in DNA touch examination. Nine donors with three shedder statuses, high, intermediate, and low, were holding the sample while tying two types of ropes, porous and non-porous. The touch sample is then sampled using two techniques on each rope: double swab and tape lift. DNA was extracted and quantified by real-time PCR technique to determine the concentration of DNA obtained from each treatment. Twenty-four STR loci of the DNA were amplified, and the fragments were analyzed by capillary electrophoresis. Two PCR cycles were chosen to determine the effect of adding cycles on the concentration of DNA that was not successfully amplified. The results of this study indicate that the quantity of touch DNA has a greater influence on the success rate of STR amplification. Each allele on 20 STR CODIS Loci failed to amplify from touch DNA concentration below 0.0625 ng/µl. It is shown that the longer the target allele at each locus, the easier it is for allelic drop-out to occur. However, the optimal STR locus length for DNA testing is under 200 nucleotides.
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