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首页> 外文期刊>Forensic science international. Genetics >Inter-laboratory evaluation of SNP-based forensic identification by massively parallel sequencing using the Ion PGM (TM)
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Inter-laboratory evaluation of SNP-based forensic identification by massively parallel sequencing using the Ion PGM (TM)

机译:使用Ion PGM(TM)进行大规模平行测序,对基于SNP的法医鉴定进行实验室间评估

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摘要

Next generation sequencing (NGS) offers the opportunity to analyse forensic DNA samples and obtain massively parallel coverage of targeted short sequences with the variants they carry. We evaluated the levels of sequence coverage, genotyping precision, sensitivity and mixed DNA patterns of a prototype version of the first commercial forensic NGS kit: the HID-Ion AmpliSeq (TM) Identity Panel with 169-markers designed for the Ion PGM (TM) system. Evaluations were made between three laboratories following closely matched Ion PGM (TM) protocols and a simple validation framework of shared DNA controls. The sequence coverage obtained was extensive for the bulk of SNPs targeted by the HID-Ion AmpliSeq (TM) Identity Panel. Sensitivity studies showed 90-95% of SNP genotypes could be obtained from 25 to 100 pg of input DNA. Genotyping concordance tests included Coriell cell-line control DNA analyses checked against whole-genome sequencing data from 1000 Genomes and Complete Genomics, indicating a very high concordance rate of 99.8%. Discordant genotypes detected in rs1979255, rs1004357, rs938283, rs2032597 and rs2399332 indicate these loci should be excluded from the panel. Therefore, the HID-Ion AmpliSeq (TM) Identity Panel and Ion PGM (TM) system provide a sensitive and accurate forensic SNP genotyping assay. However, low-level DNA produced much more varied sequence coverage and in forensic use the Ion PGM (TM) system will require careful calibration of the total samples loaded per chip to preserve the genotyping reliability seen in routine forensic DNA. Furthermore, assessments of mixed DNA indicate the user's control of sequence analysis parameter settings is necessary to ensure mixtures are detected robustly. Given the sensitivity of Ion PGM (TM), this aspect of forensic genotyping requires further optimisation before massively parallel sequencing is applied to routine casework. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
机译:下一代测序(NGS)提供了分析法医DNA样本并获得带有其携带的变异体的目标短序列的大规模平行报道的机会。我们评估了第一个商业法医NGS试剂盒原型的序列覆盖水平,基因分型精度,敏感性和混合DNA模式:HID-Ion AmpliSeq(TM)Identity Panel,带有为Ion PGM(TM)设计的169个标记系统。在三个实验室之间按照紧密匹配的离子PGM(TM)方案和共享的DNA对照的简单验证框架进行了评估。对于HID离子AmpliSeq(TM)身份鉴定小组靶向的大部分SNP,获得的序列覆盖范围广泛。敏感性研究表明,从25到100 pg的输入DNA可以获得90-95%的SNP基因型。基因分型一致性测试包括针对来自1000个基因组和完全基因组学的全基因组测序数据检查的Coriell细胞系对照DNA分析,表明非常高的一致性率为99.8%。 rs1979255,rs1004357,rs938283,rs2032597和rs2399332中检测到的不一致基因型表明应将这些基因座从面板中排除。因此,HID离子AmpliSeq(TM)Identity Panel和Ion PGM(TM)系统提供了灵敏而准确的法医SNP基因分型测定法。但是,低级DNA产生的序列覆盖范围要大得多,在法医应用中,Ion PGM(TM)系统将需要仔细校准每个芯片上装载的总样品,以保持常规法医DNA中所见的基因分型可靠性。此外,对混合DNA的评估表明,用户需要控制序列分析参数设置,以确保可靠地检测混合物。考虑到Ion PGM(TM)的敏感性,在大规模并行测序应用于常规案例研究之前,法医基因分型的这一方面需要进一步优化。 (C)2015 Elsevier Ireland Ltd.保留所有权利。

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