Churchill Jennifer D, Novroski Nicole M M, King Jonathan L, Seah Lay Hong, Budowle Bruce
Center for Human Identification, University of North Texas Health Science Center, 3500 Camp Bowie Blvd., Fort Worth, TX 76107, USA.
Center for Human Identification, University of North Texas Health Science Center, 3500 Camp Bowie Blvd., Fort Worth, TX 76107, USA.
Forensic Sci Int Genet. 2017 Sep;30:81-92. doi: 10.1016/j.fsigen.2017.06.004. Epub 2017 Jun 17.
The MiSeq FGx Forensic Genomics System (Illumina) enables amplification and massively parallel sequencing of 59 STRs, 94 identity informative SNPs, 54 ancestry informative SNPs, and 24 phenotypic informative SNPs. Allele frequency and population statistics data were generated for the 172 SNP loci included in this panel on four major population groups (Chinese, African Americans, US Caucasians, and Southwest Hispanics). Single-locus and combined random match probability values were generated for the identity informative SNPs. The average combined STR and identity informative SNP random match probabilities (assuming independence) across all four populations were 1.75E-67 and 2.30E-71 with length-based and sequence-based STR alleles, respectively. Ancestry and phenotype predictions were obtained using the ForenSeq™ Universal Analysis System (UAS; Illumina) based on the ancestry informative and phenotype informative SNP profiles generated for each sample. Additionally, performance metrics, including profile completeness, read depth, relative locus performance, and allele coverage ratios, were evaluated and detailed for the 725 samples included in this study. While some genetic markers included in this panel performed notably better than others, performance across populations was generally consistent. The performance and population data included in this study support that accurate and reliable profiles were generated and provide valuable background information for laboratories considering internal validation studies and implementation.
MiSeq FGx法医基因组学系统(Illumina公司)能够对59个短串联重复序列(STR)、94个个体识别信息性单核苷酸多态性(SNP)、54个祖先信息性SNP和24个表型信息性SNP进行扩增和大规模平行测序。针对该检测板中包含的172个SNP位点,在四个主要人群组(中国人、非裔美国人、美国白种人和西南西班牙裔)中生成了等位基因频率和群体统计数据。为个体识别信息性SNP生成了单基因座和联合随机匹配概率值。在所有四个人群中,基于长度的STR等位基因和基于序列的STR等位基因的平均联合STR和个体识别信息性SNP随机匹配概率(假设独立)分别为1.75E-67和2.30E-71。使用ForenSeq™通用分析系统(UAS;Illumina公司),根据为每个样本生成的祖先信息性和表型信息性SNP谱,获得祖先和表型预测结果。此外,还对本研究中包含的725个样本的性能指标进行了评估和详细分析,包括谱完整性、读取深度、相对基因座性能和等位基因覆盖率。虽然该检测板中包含的一些遗传标记的表现明显优于其他标记,但各人群的表现总体一致。本研究中包含的性能和群体数据支持生成了准确可靠的谱,并为考虑进行内部验证研究和实施的实验室提供了有价值的背景信息。