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使用靶向半导体测序对数百个Y染色体单核苷酸多态性进行同步分析,以实现高分辨率父系谱系分类。

Simultaneous analysis of hundreds of Y-chromosomal SNPs for high-resolution paternal lineage classification using targeted semiconductor sequencing.

作者信息

Ralf Arwin, van Oven Mannis, Zhong Kaiyin, Kayser Manfred

机构信息

Department of Forensic Molecular Biology, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands.

出版信息

Hum Mutat. 2015 Jan;36(1):151-9. doi: 10.1002/humu.22713. Epub 2014 Nov 27.

DOI:10.1002/humu.22713
PMID:25338970
Abstract

SNPs from the non-recombining part of the human Y chromosome (Y-SNPs) are informative to classify paternal lineages in forensic, genealogical, anthropological, and evolutionary studies. Although thousands of Y-SNPs were identified thus far, previous Y-SNP multiplex tools target only dozens of markers simultaneously, thereby restricting the provided Y-haplogroup resolution and limiting their applications. Here, we overcome this shortcoming by introducing a high-resolution multiplex tool for parallel genotyping-by-sequencing of 530 Y-SNPs using the Ion Torrent PGM platform, which allows classification of 432 worldwide Y haplogroups. Contrary to previous Y-SNP multiplex tools, our approach covers branches of the entire Y tree, thereby maximizing the paternal lineage classification obtainable. We used a default DNA input amount of 10 ng per reaction but preliminary sensitivity testing revealed positive results from as little as 100 pg input DNA. Furthermore, we demonstrate that sample pooling using barcodes is feasible, allowing increased throughput for lower per-sample costs. In addition to the wetlab protocol, we provide a software tool for automated data quality control and haplogroup classification. The unique combination of ultra-high marker density and high sensitivity achievable from low amounts of potentially degraded DNA makes this new multiplex tool suitable for a wide range of Y-chromosome applications.

摘要

来自人类Y染色体非重组部分的单核苷酸多态性(Y-SNPs)在法医、族谱、人类学和进化研究中有助于对父系谱系进行分类。尽管迄今为止已鉴定出数千个Y-SNPs,但以往的Y-SNP多重检测工具同时仅针对数十个标记,从而限制了所提供的Y单倍群分辨率并限制了其应用。在此,我们通过引入一种高分辨率多重检测工具来克服这一缺点,该工具利用Ion Torrent PGM平台对530个Y-SNPs进行平行测序基因分型,可对432个全球Y单倍群进行分类。与以往的Y-SNP多重检测工具不同,我们的方法覆盖了整个Y染色体树的各个分支,从而使可获得的父系谱系分类最大化。我们每个反应使用10 ng的默认DNA输入量,但初步敏感性测试显示,输入低至100 pg的DNA也能得到阳性结果。此外,我们证明使用条形码进行样本合并是可行的,可提高通量并降低每个样本的成本。除了湿实验室方案外,我们还提供了一个用于自动数据质量控制和单倍群分类的软件工具。这种新的多重检测工具具有超高的标记密度和从少量潜在降解DNA中可实现的高灵敏度的独特组合,适用于广泛的Y染色体应用。

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