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一种用于血统调查的34重常染色体单核苷酸多态性单碱基延伸检测法。

A 34-plex autosomal SNP single base extension assay for ancestry investigations.

作者信息

Phillips C, Fondevila M, Lareau Maria Victoria

机构信息

Forensic Genetics Unit, Institute of Legal Medicine, University of Santiago de Compostela, Santiago de Compostela, Spain.

出版信息

Methods Mol Biol. 2012;830:109-26. doi: 10.1007/978-1-61779-461-2_8.

DOI:10.1007/978-1-61779-461-2_8
PMID:22139656
Abstract

Ancestry inference based on autosomal markers remains a niche approach in forensic analysis: most laboratories feel more secure with a review of the cumulative STR profile frequencies in a range of relevant populations with the possible additional analysis of mitochondrial and/or Y-chromosome variability. However, a proportion of autosomal single nucleotide polymorphisms (SNPs) show very well-differentiated allele frequencies among global population-groups. Furthermore, such ancestry informative marker SNPs (AIM-SNPs) lend themselves to relatively straightforward typing with short-amplicon PCR and multiplexed single base extension reactions using the same capillary electrophoresis detectors required for the sequencing and STR genotyping of mainstream forensic markers. In this chapter, we describe a 34 AIM-SNP multiplex that is robust enough for the analysis of challenging, often highly degraded DNA typical of much of routine forensic casework. We also outline in detail the in-silico procedures necessary for collecting parental population reference data from the SPSmart SNP databases and performing ancestry inference of single AIM-SNP profiles or large-scale population data using the companion ancestry analysis website of Snipper. Two casework examples are described that show, in both cases, that an inference of likely ancestry using AIM-SNPs helped the identification of highly degraded skeletal material.

摘要

基于常染色体标记的血统推断在法医分析中仍然是一种小众方法

大多数实验室通过审查一系列相关人群中累积的STR图谱频率,并可能额外分析线粒体和/或Y染色体变异性,会感觉更有把握。然而,一部分常染色体单核苷酸多态性(SNP)在全球人群组中显示出分化良好的等位基因频率。此外,这类具有血统信息的标记SNP(AIM-SNP)适合用短扩增子PCR进行相对简单的分型,并使用主流法医标记测序和STR基因分型所需的相同毛细管电泳检测器进行多重单碱基延伸反应。在本章中,我们描述了一个包含34个AIM-SNP的多重检测体系,其足够稳健,可用于分析许多常规法医案件中常见的具有挑战性的、通常高度降解的DNA。我们还详细概述了从SPSmart SNP数据库收集亲代群体参考数据以及使用Snipper配套的血统分析网站对单个AIM-SNP图谱或大规模群体数据进行血统推断所需的计算机程序。文中描述了两个案例,在这两个案例中,使用AIM-SNP推断可能的血统都有助于识别高度降解的骨骼材料。

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A 34-plex autosomal SNP single base extension assay for ancestry investigations.一种用于血统调查的34重常染色体单核苷酸多态性单碱基延伸检测法。
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