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应用定制单倍型调用程序分析 56 个微单倍型的基于序列的数据。

Application of a custom haplotype caller to analyze sequence-based data of 56 microhaplotypes.

机构信息

Department of Forensic Medicine, Yonsei University College of Medicine, Seoul 03722, Republic of Korea; Graduate School of Medical Science, Brain Korea 21 Project, Yonsei University, Seoul 03722, Republic of Korea.

Department of Forensic Medicine, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.

出版信息

Forensic Sci Int Genet. 2022 Nov;61:102778. doi: 10.1016/j.fsigen.2022.102778. Epub 2022 Sep 18.

DOI:10.1016/j.fsigen.2022.102778
PMID:36166997
Abstract

Microhaplotypes (microhaps) are recently introduced markers that aim to complement the limitations of conventional forensic markers such as short tandem repeats (STRs) and single nucleotide polymorphisms (SNPs). With the potential of microhaps in forensics becoming clearer through massively parallel sequencing (MPS), MPS-based studies on microhaps are being actively reported. However, simpler workflow schemes for the generation and analysis of MPS data are still required to facilitate the practical application of MPS in forensics. In this study, we developed an in-house MPS panel that simultaneously amplifies 56 microhaps and a custom haplotype caller, Visual Microhap. The developed tool works on a web browser and provides four analysis options to extract SNP-based haplotypes from sequence-based data obtained by STRait Razor 3.0. To demonstrate the utility of the MPS panel and data analysis workflow scheme, we also analyzed 56 microhaps of 286 samples from four populations (African-American, Caucasian, Hispanic, and Korean). The average effective number of alleles (A) for the four groups was 3.45, ranging from 1.74 to 6.98. Forensic statistical parameters showed that this microhap panel is more powerful than conventional autosomal STRs for human identification. Meanwhile, the 56-plex panel mostly comprised microhaps with high Ae; however, the four populations were grossly distinguishable from each other by cluster analysis. Consequently, the developed in-house MPS panel for 56 microhaps and the adopted workflow using open-source tools can increase the utility of microhap MPS in forensic research and practice.

摘要

微单倍型(microhap)是最近引入的标记物,旨在弥补传统法医标记物(如短串联重复序列(STRs)和单核苷酸多态性(SNPs))的局限性。随着 MPS 对微单倍型在法医学中应用潜力的不断明晰,基于 MPS 的微单倍型研究正在积极开展。然而,为了促进 MPS 在法医学中的实际应用,仍需要更简单的 MPS 数据生成和分析工作流程方案。在本研究中,我们开发了一种内部 MPS 面板,该面板可同时扩增 56 个微单倍型和一个定制的单体型调用器,即 Visual Microhap。该开发工具可在网络浏览器上运行,并提供四个分析选项,可从 STRait Razor 3.0 获得的基于序列的数据中提取基于 SNP 的单体型。为了证明 MPS 面板和数据分析工作流程方案的实用性,我们还分析了来自四个群体(非裔美国人、白种人、西班牙裔和韩国人)的 286 个样本的 56 个微单倍型。四个群体的平均有效等位基因数(A)为 3.45,范围为 1.74 至 6.98。法医统计参数表明,与传统的常染色体 STR 相比,该微单倍型面板在人类识别方面更具威力。同时,56 plex 面板主要由高 Ae 的微单倍型组成;然而,通过聚类分析,四个群体之间存在明显差异。因此,开发的用于 56 个微单倍型的内部 MPS 面板和采用的开源工具工作流程可以提高微单倍型 MPS 在法医研究和实践中的实用性。

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