Performance comparison of a previously validated microhaplotype panel and a forensic STR panel for DNA mixture analysis

IF 3.2 2区 医学 Q2 GENETICS & HEREDITY
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Abstract

Short Tandem Repeats (STRs) are the most widespread markers in forensic genetics. However, STR stutter peaks can mask alleles from a minor contributor when analysing mixtures, hindering the interpretation of complex profiles. In this study we compared the performance of a previously described panel of microhaplotypes (MHs), an alternative type of forensic marker, against a standard STR kit. The parameters evaluated included: capability of determining the minimum number of contributors in the mixture; percentages of allele drop-outs and drop-ins; retrieval of alleles belonging to the minor contributor, and estimation of likelihood ratio (LR) values. In addition, the capacity of EuroForMix software to estimate each donor’s percentage of contribution was tested, as well as the impact on results when using manually, or automatically prepared libraries. The MH panel showed better performance than STRs for the detection of 2-contributor mixtures, but the lower degree of polymorphism per MH marker hindered the task of deconvolution with multiple contributors. MHs presented higher drop-in rates and lower drop-out rates, a higher capability to recover the minor contributor’s alleles and provided higher LR values than STRs, likely due to the much higher number of loci combined in the panel. Estimations of contributor ratios using EuroForMix showed promising results and marginal differences were found in these values between manually and automatically prepared libraries. Overall, results showed that the mixture detection performance of the MH panel was better or equal to the standard forensic autosomal STR panel, indicating microhaplotypes are informative markers for this purpose.

用于 DNA 混合物分析的先前验证的微单体型面板和法医 STR 面板的性能比较
短串联重复序列(STR)是法医遗传学中最常见的标记。然而,在分析混合物时,STR 的滞后峰可能会掩盖来自次要贡献者的等位基因,从而妨碍对复杂特征的解释。在这项研究中,我们比较了之前描述的微单体型(MHs)面板(另一种法医标记)与标准 STR 试剂盒的性能。评估的参数包括:确定混合物中最小贡献者数量的能力;等位基因丢失和丢失的百分比;检索属于次要贡献者的等位基因,以及估计似然比(LR)值。此外,还测试了 EuroForMix 软件估计每个供体贡献百分比的能力,以及使用手动或自动准备的文库对结果的影响。在检测 2 个供体混合物时,MH 面板比 STR 表现出更好的性能,但每个 MH 标记的多态性程度较低,妨碍了多供体解旋任务。与 STR 相比,MHs 的插入率更高,插入率更低,恢复小贡献者等位基因的能力更强,LR 值更高,这可能是由于面板中结合的位点数量要多得多。使用 EuroForMix 对贡献者比率的估计显示出良好的结果,在这些数值上,人工和自动准备的文库之间存在微小差异。总之,结果显示 MH 面板的混合物检测性能优于或等于标准法医常染色体 STR 面板,表明微单体型是这方面的信息标记。
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来源期刊
CiteScore
7.50
自引率
32.30%
发文量
132
审稿时长
11.3 weeks
期刊介绍: Forensic Science International: Genetics is the premier journal in the field of Forensic Genetics. This branch of Forensic Science can be defined as the application of genetics to human and non-human material (in the sense of a science with the purpose of studying inherited characteristics for the analysis of inter- and intra-specific variations in populations) for the resolution of legal conflicts. The scope of the journal includes: Forensic applications of human polymorphism. Testing of paternity and other family relationships, immigration cases, typing of biological stains and tissues from criminal casework, identification of human remains by DNA testing methodologies. Description of human polymorphisms of forensic interest, with special interest in DNA polymorphisms. Autosomal DNA polymorphisms, mini- and microsatellites (or short tandem repeats, STRs), single nucleotide polymorphisms (SNPs), X and Y chromosome polymorphisms, mtDNA polymorphisms, and any other type of DNA variation with potential forensic applications. Non-human DNA polymorphisms for crime scene investigation. Population genetics of human polymorphisms of forensic interest. Population data, especially from DNA polymorphisms of interest for the solution of forensic problems. DNA typing methodologies and strategies. Biostatistical methods in forensic genetics. Evaluation of DNA evidence in forensic problems (such as paternity or immigration cases, criminal casework, identification), classical and new statistical approaches. Standards in forensic genetics. Recommendations of regulatory bodies concerning methods, markers, interpretation or strategies or proposals for procedural or technical standards. Quality control. Quality control and quality assurance strategies, proficiency testing for DNA typing methodologies. Criminal DNA databases. Technical, legal and statistical issues. General ethical and legal issues related to forensic genetics.
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