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评估 Ion AmpliSeq™ PhenoTrivium 面板:基于 MPS 的法医学样本分析方法用于种族和表型预测的挑战。

Evaluation of the Ion AmpliSeq™ PhenoTrivium Panel: MPS-Based Assay for Ancestry and Phenotype Predictions Challenged by Casework Samples.

机构信息

Department of Forensic Genetics, Institute of Legal Medicine, Ludwig Maximilian University of Munich, Nußbaumstraße 26, 80336 Munich, Bavaria, Germany.

Human Identification Group, Thermo Fisher Scientific, 180 Oyster Point Blvd, South San Francisco, CA 94080, USA.

出版信息

Genes (Basel). 2020 Nov 25;11(12):1398. doi: 10.3390/genes11121398.

Abstract

As the field of forensic DNA analysis has started to transition from genetics to genomics, new methods to aid in crime scene investigations have arisen. The development of informative single nucleotide polymorphism (SNP) markers has led the forensic community to question if DNA can be a reliable "eye-witness" and whether the data it provides can shed light on unknown perpetrators. We have developed an assay called the Ion AmpliSeq™ PhenoTrivium Panel, which combines three groups of markers: 41 phenotype- and 163 ancestry-informative autosomal SNPs together with 120 lineage-specific Y-SNPs. Here, we report the results of testing the assay's sensitivity and the predictions obtained for known reference samples. Moreover, we present the outcome of a blind study performed on real casework samples in order to understand the value and reliability of the information that would be provided to police investigators. Furthermore, we evaluated the accuracy of admixture prediction in Converge™ Software. The results show the panel to be a robust and sensitive assay which can be used to analyze casework samples. We conclude that the combination of the obtained predictions of phenotype, biogeographical ancestry, and male lineage can serve as a potential lead in challenging police investigations such as cold cases or cases with no suspect.

摘要

随着法医 DNA 分析领域已开始从遗传学向基因组学转变,新的方法也应运而生,以辅助犯罪现场调查。信息性单核苷酸多态性 (SNP) 标记的开发促使法医界质疑 DNA 是否可以成为可靠的“目击者”,以及它所提供的数据是否可以揭示未知犯罪者的情况。我们开发了一种名为 Ion AmpliSeq™ PhenoTrivium 面板的检测方法,该方法结合了三组标记物:41 个表型和 163 个祖先信息性常染色体 SNPs,以及 120 个谱系特异性 Y-SNPs。在这里,我们报告了该检测方法的灵敏度测试结果和对已知参考样本的预测结果。此外,我们还介绍了在实际案例样本上进行的盲法研究的结果,以了解为警方调查人员提供的信息的价值和可靠性。此外,我们还评估了 Converge™ 软件中混合预测的准确性。结果表明,该面板是一种强大且敏感的检测方法,可用于分析案例样本。我们得出结论,获得的表型、生物地理祖先和男性谱系的预测结果可以作为解决具有挑战性的警方调查(如冷案或无嫌疑人案件)的潜在线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cc1/7760956/701fbff7c209/genes-11-01398-g001.jpg

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