Suppr超能文献

基于大规模平行测序的线粒体DNA样本混合分析

Massively parallel sequencing-enabled mixture analysis of mitochondrial DNA samples.

作者信息

Churchill Jennifer D, Stoljarova Monika, King Jonathan L, Budowle Bruce

机构信息

Center for Human Identification, University of North Texas Health Science Center, 3500 Camp Bowie Blvd, CBH-250, Fort Worth, TX, 76107, USA.

Department of Chemistry and Biotechnology, Tallinn University of Technology, Tallinn, Estonia.

出版信息

Int J Legal Med. 2018 Sep;132(5):1263-1272. doi: 10.1007/s00414-018-1799-3. Epub 2018 Feb 22.

Abstract

The mitochondrial genome has a number of characteristics that provide useful information to forensic investigations. Massively parallel sequencing (MPS) technologies offer improvements to the quantitative analysis of the mitochondrial genome, specifically the interpretation of mixed mitochondrial samples. Two-person mixtures with nuclear DNA ratios of 1:1, 5:1, 10:1, and 20:1 of individuals from different and similar phylogenetic backgrounds and three-person mixtures with nuclear DNA ratios of 1:1:1 and 5:1:1 were prepared using the Precision ID mtDNA Whole Genome Panel and Ion Chef, and sequenced on the Ion PGM or Ion S5 sequencer (Thermo Fisher Scientific, Waltham, MA, USA). These data were used to evaluate whether and to what degree MPS mixtures could be deconvolved. Analysis was effective in identifying the major contributor in each instance, while SNPs from the minor contributor's haplotype only were identified in the 1:1, 5:1, and 10:1 two-person mixtures. While the major contributor was identified from the 5:1:1 mixture, analysis of the three-person mixtures was more complex, and the mixed haplotypes could not be completely parsed. These results indicate that mixed mitochondrial DNA samples may be interpreted with the use of MPS technologies.

摘要

线粒体基因组具有许多可为法医调查提供有用信息的特征。大规模平行测序(MPS)技术改进了线粒体基因组的定量分析,特别是对混合线粒体样本的解读。使用Precision ID线粒体DNA全基因组分析试剂盒和Ion Chef制备了来自不同和相似系统发育背景个体的核DNA比例为1:1、5:1、10:1和20:1的两人混合样本以及核DNA比例为1:1:1和5:1:1的三人混合样本,并在Ion PGM或Ion S5测序仪(美国马萨诸塞州沃尔瑟姆市赛默飞世尔科技公司)上进行测序。这些数据用于评估MPS混合样本是否以及在何种程度上可以解卷积。分析在每种情况下都有效地识别出了主要贡献者,而仅在1:1、5:1和10:1的两人混合样本中识别出了次要贡献者单倍型的单核苷酸多态性(SNP)。虽然从5:1:1的混合样本中识别出了主要贡献者,但三人混合样本的分析更为复杂,混合单倍型无法完全解析。这些结果表明,使用MPS技术可以解读混合线粒体DNA样本。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验