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用于法医降解DNA样本人类身份鉴定的43个插入/缺失位点的新型组合:开发与验证

A Novel Panel of 43 Insertion/Deletion Loci for Human Identifications of Forensic Degraded DNA Samples: Development and Validation.

作者信息

Jin Rui, Cui Wei, Fang Yating, Jin Xiaoye, Wang Hongdan, Lan Qiong, Guo Yuxin, Chen Chong, Zhang Xingru, Zhu Bofeng

机构信息

Key Laboratory of Shaanxi Province for Craniofacial Precision Medicine Research, College of Stomatology, Xi'an Jiaotong University, Xi'an, China.

Clinical Research Center of Shaanxi Province for Dental and Maxillofacial Diseases, College of Stomatology, Xi'an Jiaotong University, Xi'an, China.

出版信息

Front Genet. 2021 Mar 11;12:610540. doi: 10.3389/fgene.2021.610540. eCollection 2021.

DOI:10.3389/fgene.2021.610540
PMID:33777093
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7990895/
Abstract

Insertion/deletion polymorphism is a promising genetic marker in the forensic genetic fields, especially in the forensic application of degraded sample at crime scene. In this research, a novel five-dye multiplex amplification panel containing 43 highly polymorphic Insertion/deletion (InDel) loci and one Amelogenin gene locus is designed and constructed in-house for the individual identification in East Asian populations. The amplicon sizes of 43 InDel loci are less than 200 bp, which help to ensure that full allele profiles can be obtained from degraded DNA sample. A series of optimizations and developmental validations including optimization of PCR conditions, detection efficiency of the degraded and casework samples, sensitivity, reproducibility, precision, tolerance for inhibitors, species specificity and DNA mixtures are performed according to the Scientific Working Group on DNA Analysis Methods (SWGDAM) guideline. The results of the internal validation demonstrated that this novel InDel panel was a reliable, sensitive and accurate system with good tolerances to different inhibitors, and performed the considerable detection efficiency for the degraded or mixed samples, which could be used in the forensic applications.

摘要

插入/缺失多态性是法医遗传学领域一种很有前景的遗传标记,尤其适用于犯罪现场降解样本的法医鉴定。在本研究中,自行设计并构建了一个新型的五色荧光多重扩增体系,包含43个高度多态性的插入/缺失(InDel)基因座和一个牙釉蛋白基因座,用于东亚人群的个体识别。43个InDel基因座的扩增子大小均小于200 bp,这有助于确保从降解的DNA样本中获得完整的等位基因图谱。根据DNA分析方法科学工作组(SWGDAM)的指南,进行了一系列优化和方法学验证,包括PCR条件优化、降解样本和实际案件样本的检测效率、灵敏度、重复性、精密度、对抑制剂的耐受性、物种特异性以及DNA混合物分析等。内部验证结果表明,这个新型的InDel体系是一个可靠、灵敏且准确的系统,对不同抑制剂具有良好的耐受性,对降解或混合样本具有相当高的检测效率,可用于法医鉴定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c470/7990895/829c1c1eb26e/fgene-12-610540-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c470/7990895/4b5f68718e6e/fgene-12-610540-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c470/7990895/afbd68a37d0f/fgene-12-610540-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c470/7990895/8b90f66a2a7e/fgene-12-610540-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c470/7990895/b12990faca2c/fgene-12-610540-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c470/7990895/829c1c1eb26e/fgene-12-610540-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c470/7990895/4b5f68718e6e/fgene-12-610540-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c470/7990895/afbd68a37d0f/fgene-12-610540-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c470/7990895/8b90f66a2a7e/fgene-12-610540-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c470/7990895/b12990faca2c/fgene-12-610540-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c470/7990895/829c1c1eb26e/fgene-12-610540-g005.jpg

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