Guo Fei, Yu Jiao, Zhang Lu, Li Jun
Department of Forensic Medicine, Criminal Investigation Police University of China, No. 83, Tawan Street, Huanggu District, Shenyang 110854, Liaoning, PR China.
Criminal Science and Technology Institute of Liaoning Province, No. 2, Qishan Middle Road, Huanggu District, Shenyang 110032, Liaoning, PR China.
Forensic Sci Int Genet. 2017 Nov;31:135-148. doi: 10.1016/j.fsigen.2017.09.003. Epub 2017 Sep 8.
The ForenSeq™ DNA Signature Prep Kit (ForenSeq Kit) is designed to detect more than 200 forensically relevant markers in a single reaction on the MiSeq FGx™ Forensic Genomics System (MiSeq FGx System), including Amelogenin, 27 autosomal short tandem repeats (A-STRs), 7 X chromosomal STRs (X-STRs), 24 Y chromosomal STRs (Y-STRs) and 94 identity-informative single nucleotide polymorphisms (iSNPs) with the option to contain 22 phenotypic-informative SNPs (pSNPs) and 56 ancestry-informative SNPs (aSNPs). In this study, we evaluated the MiSeq FGx System on three major parts: methodological optimization (DNA extraction, sample quantification, library normalization, diluted libraries concentration, and sample-to-cell arrangement), massively parallel sequencing (MPS) performance (depth of coverage, sequence coverage ratio, and allele coverage ratio), and ForenSeq Kit characteristics (repeatability and concordance, sensitivity, mixture, stability and case-type samples). Results showed that quantitative polymerase chain reaction (qPCR)-based sample quantification and library normalization and the appropriate number of pooled libraries and concentration of diluted libraries provided a greater level of MPS performance and repeatability. Repeatable and concordant genotypes were obtained by the ForenSeq Kit. Full profiles were obtained from ≥100pg input DNA for STRs and ≥200pg for SNPs. A sample with ≥5% minor contributors was considered as a mixture by imbalanced allele coverage ratio distribution, and full profiles from minor contributors were easily detected between 9:1 and 1:9 mixtures with known reference profiles. The ForenSeq Kit tolerated considerable concentrations of inhibitors like ≤200μM hematin and ≤50μg/ml humic acid, and >56% STR profiles and >88% SNP profiles were obtained from ≥200-bp degraded samples. Also, it was adapted to case-type samples. As a whole, the ForenSeq Kit is a well-performed, robust, reliable, reproducible and highly informative assay, and it can fully meet requirements for human identification. Further, sensitive QC indicator and automated sample comparison function in the ForenSeq™ Universal Analysis Software are quite helpful, so that we can concentrate on questionable genotypes and avoid tedious and time-consuming labor to maximum the time spent in data analysis.
ForenSeq™ DNA 特征制备试剂盒(ForenSeq 试剂盒)旨在通过 MiSeq FGx™ 法医基因组学系统(MiSeq FGx 系统)上的单次反应检测 200 多个法医相关标记,包括牙釉蛋白、27 个常染色体短串联重复序列(A-STR)、7 个 X 染色体 STR(X-STR)、24 个 Y 染色体 STR(Y-STR)以及 94 个身份信息单核苷酸多态性(iSNP),还可选择包含 22 个表型信息 SNP(pSNP)和 56 个祖先信息 SNP(aSNP)。在本研究中,我们从三个主要方面对 MiSeq FGx 系统进行了评估:方法优化(DNA 提取、样本定量、文库标准化、稀释文库浓度以及样本与细胞排列)、大规模平行测序(MPS)性能(覆盖深度、序列覆盖率和等位基因覆盖率)以及 ForenSeq 试剂盒特性(重复性和一致性、灵敏度、混合物、稳定性和案件类型样本)。结果表明,基于定量聚合酶链反应(qPCR)的样本定量和文库标准化以及合适数量的混合文库和稀释文库浓度可提供更高水平的 MPS 性能和重复性。ForenSeq 试剂盒获得了可重复且一致的基因型。对于 STR,输入 DNA≥100pg 可获得完整图谱,对于 SNP 则≥200pg 可获得完整图谱。等位基因覆盖率分布不均衡时,次要贡献者比例≥5%的样本被视为混合物,在 9:1 至 1:9 的已知参考图谱混合物中,次要贡献者的完整图谱很容易被检测到。ForenSeq 试剂盒可耐受相当浓度的抑制剂,如≤200μM 血红素和≤50μg/ml 腐殖酸,从≥200bp 的降解样本中可获得>56%的 STR 图谱和>88%的 SNP 图谱。此外,它适用于案件类型样本。总体而言,ForenSeq 试剂盒是一种性能良好、稳健、可靠、可重复且信息丰富的检测方法,能够充分满足人类身份鉴定的要求。此外,ForenSeq™ 通用分析软件中的灵敏质量控制指标和自动样本比较功能非常有用,这样我们可以专注于可疑基因型,避免繁琐且耗时的工作,最大限度地减少数据分析所花费的时间。