评价基于序列的STR基因分型与基于长度的STR基因分型在亲属关系分析中的统计功效。

IF 2.3 3区 医学 Q1 MEDICINE, LEGAL
Huseyin Sevay, Naciye Durmus, Gonul Filoglu, Cemal Gurkan, Ozlem Bulbul
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引用次数: 0

摘要

在这项研究中,我们分析了代表4个主要关系类别的137对关系,涉及来自4个家族的49名土耳其人,以评估在相同STR基因座覆盖范围内,使用基于序列的基因分型方法与基于长度的基因分型方法时,与似然比(LR)相关的统计能力的潜在增益。为此,使用了MPS Precision ID GlobalFiler NGS STR试剂盒和CE GlobalFiler™PCR扩增试剂盒。与基于ce的基因分型获得的150个独特等位基因相比,基于mps的分析显示存在37个STR DNA序列变异和/或26个STR DNA序列侧翼区snp。考虑到大多数亲缘关系LR计算软件不容易考虑在基于mps的基因分型过程中可用的STR DNA序列变体和STR DNA序列侧翼区域SNP数据,我们实现了一个字母数字等位基因重编码系统,将这些额外的STR等等位基因数据合并到已有的等位基因调用中。在所分析的所有四种主要关系类别中,从基于ce的分型到基于mps的分型,观察到平均联合LR (cLR)显着增加,其中78.08到7,864,630.60倍增加。更具体地说,在分析的137个两两关系中的134个中,基于mps的cLR值高于使用基于ce的数据计算的cLR值。当使用CE时,四个主要关系类别中有三个的平均cLR为1000美元,唯一的例外是第三度关系,当使用MPS时,所有四个主要关系类别的平均cLR为1000美元。值得注意的是,CE和MPS三度关系的平均cLR分别为47.61和3717.31。与基于ce的基因分型相比,在充分考虑本研究提出的情况下,基于mps的基因分型提供的DNA序列变异数据在获得的cLR值方面具有统计学意义的增加。使用MPS计算cLR对二度和三度关系都有最大的影响,这两种类型的复杂/遥远的分析,因此进一步强调了MPS在亲属关系分析中的前景。虽然目前的研究表明,对于给定的病例,在相同的位点覆盖范围内,从CE基因分型到MPS基因分型,cLR可能会大幅增加,但当额外的DNA序列差异也被考虑在内时,由于MPS试剂盒使用的法医标记类型更多样化,甚至更广泛的位点覆盖范围,预计cLR会进一步增加。
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 gain in statistical power for kinship analysis using sequence-based versus length-based STR genotyping.

In this study, 137 pairwise relationships representing four major relationship categories involving 49 Turkish individuals from four families were analyzed to evaluate the potential gain in the statistical power associated with likelihood ratios (LR) when using sequence-based versus length-based genotyping methods over the same STR loci coverage. To this end, the MPS Precision ID GlobalFiler NGS STR panel Kit and CE GlobalFiler™ PCR Amplification Kit were used. MPS-based analysis revealed the presence of 37 STR DNA sequence variations and / or the presence of 26 STR DNA sequence flanking region SNPs compared to the 150 unique alleles obtained with CE-based genotyping. Considering that most kinship LR calculation software do not readily take into consideration STR DNA sequence variants and STR DNA sequence flanking region SNP data that becomes available during MPS-based genotyping, an alphanumeric allele re-coding system was implemented to incorporate such additional STR isoallelic data to the already available allele calls. Over all the four major relationship categories analyzed, a significant increase in the mean combined LR (cLR) was observed when going from CE-based to MPS-based typing, whereby a 78.08 to 7,864,630.60-fold increase was noted. More specifically, in 134 out of the 137 pairwise relationships analyzed, MPS-based cLR values were higher than those calculated using CE-based data. While the mean cLR was >1,000 for three out of the four major relationship categories when using CE, the only exception being the third degree relationships, the mean cLR was >1,000 for all the four major relationship categories when using MPS. Notably, the mean cLR obtained for the third degree relationships was 47.61 with CE and 3,717.31 with MPS. In comparison with CE-based genotyping, when fully taken into account as proposed in the current study, the DNA sequence variation data afforded by MPS-based genotyping led to a statistically significant gain in terms of cLR values obtained. The use of MPS for cLR calculations had the most impact for both the second and third degree relationships, the two complex / distant type analyzed, hence further underscoring the prospects for MPS in kinship analysis. While the current study demonstrated that cLR is likely to increase substantially upon going from CE to MPS genotyping over the same loci coverage for a given case, when the additional DNA sequence variances are also taken into consideration, further increases are expected due to the more diverse type of forensic markers and even wider loci coverages used by MPS kits.

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来源期刊
CiteScore
5.80
自引率
9.50%
发文量
165
审稿时长
1 months
期刊介绍: The International Journal of Legal Medicine aims to improve the scientific resources used in the elucidation of crime and related forensic applications at a high level of evidential proof. The journal offers review articles tracing development in specific areas, with up-to-date analysis; original articles discussing significant recent research results; case reports describing interesting and exceptional examples; population data; letters to the editors; and technical notes, which appear in a section originally created for rapid publication of data in the dynamic field of DNA analysis.
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