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利用高通量测序技术评估法医遗传学中的微单倍型面板。

Evaluation of a microhaplotypes panel for forensic genetics using massive parallel sequencing technology.

机构信息

Section of Legal Medicine, Department of Excellence of Biomedical Sciences and Public Health, Polytechnic University of Marche, Ancona, Italy - Via Tronto, 60126, Torrette, Ancona (AN), Italy.

Section of Legal Medicine, Department of Excellence of Biomedical Sciences and Public Health, Polytechnic University of Marche, Ancona, Italy - Via Tronto, 60126, Torrette, Ancona (AN), Italy.

出版信息

Forensic Sci Int Genet. 2019 Jul;41:120-127. doi: 10.1016/j.fsigen.2019.04.009. Epub 2019 May 1.

Abstract

Massive parallel DNA sequencing (MPS) makes it possible to explore a new type of genetic marker, known as microhaplotypes or microhaps. These loci were recently introduced in the landscape of forensic genetic and appear to be useful for identification purposes, reconstruction of family relationships, ancestry prediction and DNA mixtures deconvolution. Microhaplotypes loci, based on 89 loci in ALFRED, were selected and their genetic variations in 100 Italian individuals were evaluated by using MPS, in order to make inference about utility of a set of microhaps in forensic genetics. After MPS, the panel was reduced to 87 microhaps, comprised of 266 different SNPs and spread across 22 human autosomes. Genotype and haplotype frequencies were estimated, as well as the effective number of alleles at each locus (A), which relates to the usefulness of the locus in resolution of relationships and deconvolution of DNA mixtures. Overall, the A values for the 87 microhaps range from 1.010 to 8.344, with about 80% showing values greater than 2.0. Noteworthy, 32 microhaps display A values greater than 3.0 and 18 loci A above 4.0. To explore the suitability of microhaplotypes in mixture deconvolution, the probability of detecting a mixture, as a function of A, was inferred for different groups of loci. Considering the fourteen loci with A between 3.0 and 3.999 the probability of detecting a mixture was at least 0.99973, while considering the ten loci with Ae between 4.0 and 4.999 the probability was at least 0.99998. Moreover, when considering just the six loci with A between 5.0 and 5.999 the probability of detecting a mixture was at least 0.99984, while when considering just the two loci with A above 6 the probability was 0.97228. Combining these 32 MH loci, the theoretical probability of detecting a mixture was 0.999999999999973. These results make the subset of 32 loci with A above three informative for mixture resolution. The individual matching probabilities (PI) of the 87 microhaps ranged from 0.032 to 0.9802. Considering the 32 microhap loci with A greater than 3.0, the cumulative PI value was 1.6 × 10, while considering the 18 microhap loci with A above 4.0, the cumulative PI value was 2.34 × 10. Overall the results of this study confirmed the utility of microhaps in forensic genetics.

摘要

大规模并行 DNA 测序(MPS)使得探索一种新型遗传标记成为可能,这种标记被称为微单倍型或微 haps。这些基因座最近被引入法医遗传学领域,似乎在鉴定、亲属关系重建、祖源预测和 DNA 混合分解方面非常有用。基于 ALFRED 中的 89 个基因座,选择了微单倍型基因座,并通过 MPS 评估了 100 名意大利个体的遗传变异,以推断一组微单倍型在法医遗传学中的实用性。MPS 后,该面板减少到 87 个微单倍型,由 266 个不同的 SNP 组成,分布在 22 个人类常染色体上。估计了基因型和单倍型频率,以及每个基因座的有效等位基因数(A),这与基因座在解决关系和 DNA 混合物分解方面的有用性有关。总体而言,87 个微单倍型的 A 值范围为 1.010 至 8.344,约 80%的 A 值大于 2.0。值得注意的是,32 个微单倍型的 A 值大于 3.0,18 个基因座的 A 值大于 4.0。为了探索微单倍型在混合物分解中的适用性,根据不同的基因座组,推断了检测混合物的概率作为 A 的函数。考虑到 14 个 A 值在 3.0 到 3.999 之间的基因座,检测混合物的概率至少为 0.99973,而考虑到 10 个 A 值在 4.0 到 4.999 之间的基因座,概率至少为 0.99998。此外,当只考虑 A 值在 5.0 到 5.999 之间的 6 个基因座时,检测混合物的概率至少为 0.99984,而当只考虑 A 值大于 6 的 2 个基因座时,概率为 0.97228。将这 32 个微单倍型基因座结合起来,检测混合物的理论概率为 0.999999999999973。这些结果表明,A 值大于 3 的 32 个微单倍型基因座子集对于混合物分辨率很有帮助。87 个微单倍型的个体匹配概率(PI)范围为 0.032 至 0.9802。考虑到 32 个 A 值大于 3.0 的微单倍型基因座,累积 PI 值为 1.6×10,而考虑到 18 个 A 值大于 4.0 的微单倍型基因座,累积 PI 值为 2.34×10。总的来说,这项研究的结果证实了微单倍型在法医遗传学中的实用性。

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