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使用 Ion Torrent 平台检测降解 DNA 样本中早期访问 AmpliSeqTM 线粒体面板的性能。

Performance of the Early Access AmpliSeq™ Mitochondrial Panel with degraded DNA samples using the Ion Torrent™ platform.

机构信息

University of Technology Sydney, Centre for Forensic Science, Sydney, NSW, Australia.

出版信息

Electrophoresis. 2018 Nov;39(21):2776-2784. doi: 10.1002/elps.201700371. Epub 2018 Jan 30.

DOI:10.1002/elps.201700371
PMID:29330875
Abstract

The Early Access AmpliSeq™ Mitochondrial Panel amplifies whole mitochondrial genomes for phylogenetic and kinship identifications, using Ion Torrent™ technology. There is currently limited information on its performance with degraded DNA, a common occurrence in forensic samples. This study evaluated the performance of the Panel with DNA samples degraded in vitro, to mimic conditions commonly found in forensic investigations. Purified DNA from five individuals was heat-treated at five time points each (125°C for 0, 30, 60, 120, and 240 min; total n = 25). The quality of DNA was assessed via a real-time DNA assay of genomic DNA and prepared for massively parallel sequencing on the Ion Torrent™ platform. Mitochondrial sequences were obtained for all samples and had an amplicon coverage averaging between 66X to 2803X. Most amplicons (157/162) displayed high coverages (452 ± 333X), while reads with less than 100X coverage were recorded in five amplicons only (90 ± 5X). Amplicon coverage was decreased with prolonged heating. At 72% strand balance, reads were well balanced between forward and reverse strands. Using a coverage threshold of ten reads per SNP, complete sequences were recovered in all samples and resolved kinship and, haplogroup relations. Additionally, the HV1 and HV2 regions of the reference and 240-min heat-treated samples (n = 10) were Sanger-sequenced for concordance. Overall, this study demonstrates the efficacy of a novel forensic Panel that recovers high quality mitochondrial sequences from degraded DNA samples.

摘要

《早期访问 AmpliSeq™ 线粒体面板》采用 Ion Torrent™ 技术扩增整个线粒体基因组,用于系统发育和亲属鉴定。目前,关于该面板在降解 DNA 方面的性能信息有限,而降解 DNA 在法医样本中很常见。本研究评估了该面板在体外降解 DNA 样本中的性能,以模拟法医调查中常见的条件。从五个人体中提取的纯化 DNA 在五个时间点(125°C 下分别为 0、30、60、120 和 240 分钟;总 n = 25)进行热处理。通过实时基因组 DNA 测定和在 Ion Torrent™ 平台上进行大规模平行测序来评估 DNA 的质量。所有样本均获得线粒体序列,平均扩增子覆盖率在 66X 至 2803X 之间。大多数扩增子(157/162)显示出高覆盖率(452 ± 333X),而只有五个扩增子(90 ± 5X)记录的读数少于 100X 覆盖率。随着加热时间的延长,扩增子覆盖率降低。在 72%链平衡时,正向和反向链之间的读数平衡良好。使用每个 SNP 十个读数的覆盖阈值,所有样本均回收了完整的序列,并解决了亲属关系和单倍群关系。此外,对参考样本和 240 分钟热处理样本(n = 10)的 HV1 和 HV2 区域进行了 Sanger 测序以验证一致性。总的来说,这项研究证明了一种新型法医面板的有效性,该面板可以从降解的 DNA 样本中回收高质量的线粒体序列。

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