DNA Diagnostic Laboratory (LDD), State University of Rio de Janeiro (UERJ), Rio de Janeiro, Brazil.
DNA Diagnostic Laboratory (LDD), State University of Rio de Janeiro (UERJ), Rio de Janeiro, Brazil.
Forensic Sci Int Genet. 2020 Jan;44:102163. doi: 10.1016/j.fsigen.2019.102163. Epub 2019 Oct 15.
The use of Y-chromosomal genetic markers in forensic investigations demands the establishment of reliable and representative DNA databases of different reference populations. The genetic characterization of the Y chromosome variation in human populations requires the analyses of haplotype frequencies allied to haplogroup determination. The present study aimed to contribute to the Brazilian database by providing 1,382 Yfiler Plus individual profiles, from 11 Brazilian states. The Yfiler Plus markers showed high haplotype diversities in all Brazilian populations (>0.9970), allowing high intra-population discrimination in forensic investigations. Pairwise genetic distances showed a homogeneity between Brazilian populations (F ≤ 0.0043; non-differentiation p-values ≥ 0.0212), indicating that admixed populations from Brazil can be represented in a single Yfiler Plus haplotype database, for forensic purposes. The performance of Haplogroup Predictor and NevGen software in haplogroup prediction based on Yfiler Plus and Yfiler haplotypes was evaluated in a subset of 416 Brazilian samples that were also genotyped for 51 Y-SNPs. In 25% of the samples, no classification or errors were found for at least one of the prediction tools or marker sets. NevGen presented lower error rates (5.52% and 8.65% with Yfiler Plus and Yfiler, respectively) than Haplogroup Predictor (16.11% with Yfiler Plus and 13.70% with Yfiler). In conclusion, both haplogroup prediction tools can be useful to direct the SNP typing, but present large error rates to be used in forensic analysis, especially in predicting African haplogroups in admixed South American populations.
在法医调查中使用 Y 染色体遗传标记需要建立不同参考人群的可靠和有代表性的 DNA 数据库。人类群体 Y 染色体变异的遗传特征需要分析单倍型频率以及单倍型群的确定。本研究旨在通过提供来自巴西 11 个州的 1382 个 Yfiler Plus 个体谱来为巴西数据库做出贡献。Yfiler Plus 标记在所有巴西人群中表现出高的单倍型多样性(>0.9970),允许在法医调查中进行高的群体内鉴别。成对遗传距离显示巴西人群之间具有同质性(F≤0.0043;非分化 p 值≥0.0212),表明巴西的混合人群可以在单一的 Yfiler Plus 单倍型数据库中代表,用于法医目的。在一个由 416 个巴西样本组成的子集(这些样本还进行了 51 个 Y-SNP 的基因分型)中评估了 Haplogroup Predictor 和 NevGen 软件在基于 Yfiler Plus 和 Yfiler 单倍型的单倍型群预测中的性能。在至少一个预测工具或标记组中,25%的样本没有分类或出现错误。NevGen 的错误率(使用 Yfiler Plus 和 Yfiler 分别为 5.52%和 8.65%)低于 Haplogroup Predictor(使用 Yfiler Plus 为 16.11%,使用 Yfiler 为 13.70%)。总之,这两种单倍型群预测工具都可以用于指导 SNP 基因分型,但在法医分析中错误率较高,特别是在预测南美洲混合人群中的非洲单倍型群时。