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用于法医DNA分型的含31个多等位基因插入缺失的多重检测板的开发。

Development of a multiplex panel with 31 multi-allelic InDels for forensic DNA typing.

作者信息

Yao Yining, Sun Kuan, Yang Qinrui, Zhou Zhihan, Qian Jinglei, Li Zhimin, Shao Chengchen, Qian Xiaoqin, Tang Qiqun, Xie Jianhui

机构信息

Department of Forensic Medicine, School of Basic Medical Sciences, Fudan University, 138 Yixueyuan Road, Shanghai, 200032, China.

Department of Fetal Medicine and Prenatal Diagnosis Center, Shanghai First Maternity and Infant Hospital, Tongji University School of Medicine, 2699 West Gaoke Rd, 201204, Shanghai, China.

出版信息

Int J Legal Med. 2023 Jan;137(1):1-12. doi: 10.1007/s00414-022-02907-w. Epub 2022 Nov 3.

Abstract

Insertion/Deletion (InDel) polymorphic genetic markers are abundant in human genomes. Diallelic InDel markers have been widely studied for forensic purposes, yet the low polymorphic information content limits their application and current InDel panels remain to be improved. In this study, multi-allelic InDels located out of low complexity sequence regions were selected in the datasets from East Asian populations, and a multiplex amplification system containing 31 multi-allelic InDel markers and the Amelogenin marker (FA-HID32plex) was constructed and optimized. The preliminary study on sensitivity, species specificity, inhibitor tolerance, mixture resolution, and the detection of degraded samples demonstrates that the FA-HID32plex is highly sensitive, specific, and robust for traces and degraded samples. The combined power of discrimination (CPD) of 31 multi-allelic InDel markers was 0.999 999 999 999 999 999 85, and the cumulative probability of exclusion (CPE) was 0.999 920 in a Chinese Han population, which indicates a high discrimination power. Altogether, the FA-HID32plex panel could provide reliable supplements or stand-alone information in individual identification and paternity testing, especially for challenging samples.

摘要

插入/缺失(InDel)多态性遗传标记在人类基因组中大量存在。双等位基因InDel标记已被广泛用于法医目的研究,但其低多态性信息含量限制了它们的应用,目前的InDel检测板仍有待改进。在本研究中,从东亚人群的数据集中选择了位于低复杂度序列区域之外的多等位基因InDel,构建并优化了一个包含31个多等位基因InDel标记和牙釉蛋白标记(FA-HID32plex)的多重扩增系统。对灵敏度、物种特异性、抑制剂耐受性、混合样本分辨率和降解样本检测的初步研究表明,FA-HID32plex对痕量和降解样本具有高度的敏感性、特异性和稳健性。在一个中国汉族人群中,31个多等位基因InDel标记的联合鉴别力(CPD)为0.999 999 999 999 999 999 85,累积排除概率(CPE)为0.999 920,这表明其具有很高的鉴别力。总之,FA-HID32plex检测板可在个体识别和亲子鉴定中提供可靠的补充信息或独立信息,特别是对于具有挑战性的样本。

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