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基于二代测序(NGS)的单核苷酸多态性(SNP)基因分型进行二级和三级亲属关系分析以及评估2045个SNP在有限或降解DNA上的性能。

Second- and third-degree kinship analysis by NGS-based SNP genotyping and evaluation of 2045-SNP performance on limited or degraded DNA.

作者信息

Asari Masaru, Takahashi Yuta, Namba Ryo, Hoshina Chisato, Mori Kanae, Okuda Katsuhiro, Shimizu Keiko

机构信息

Department of Legal Medicine, Asahikawa Medical University, Asahikawa, Japan.

Department of Legal Medicine, Asahikawa Medical University, Asahikawa, Japan.

出版信息

Forensic Sci Int. 2025 Feb;367:112346. doi: 10.1016/j.forsciint.2024.112346. Epub 2024 Dec 14.

Abstract

We developed a novel next-generation sequencing-based single-nucleotide polymorphism (SNP) genotyping method for second- and third-degree kinship analysis, and designed 1144- and 2045-SNP panels using one (Set A) and two sets (Sets A and B) of primers. These SNP loci were analyzed in 120 Japanese individuals, and likelihood ratios (LRs) for kinship discrimination were calculated to evaluate the effect of number of SNP loci in simulated analysis. Likelihood evaluation was performed using DNA profiles from two individuals, namely, the unknown and one reference relative. Genotyping of the 1144 and 2045 SNPs was informative to discriminate aunt-nephew/niece as second-degree relatives and unrelated pairs. In third-degree relationship analysis, distributions of logLRs between the unknown and a first cousin (FC) were not separated from those of unrelated individuals even in 2045-SNP genotyping. To perform enhanced discrimination of third-degree relationships, we also evaluated the effectiveness of DNA profiles from three individuals, namely, the unknown and two first cousins (2FC). A likelihood evaluation from the 2045 SNPs using 2FC was more useful than the use of FC. Our method was applied to 12 kinship cases for second- and third-degree relationship analysis, and LRs from 1144- and 2045-SNP genotypes were markedly higher than those from conventional short tandem repeat profiles. Moreover, we evaluated the performance of the 2045 SNPs using limited or degraded DNA, compared with that with a larger amount of DNA. Using 0.1 ng of non-degraded DNA, the average concordance was higher than 97 %. In analysis with heavily degraded DNA (degradation index=32.2), we also detected high concordance (85.5 %) from 2045-SNP genotypes, compared with the lower rate (52.4 %) from 21 short tandem repeat profiles. Our method should be highly sensitive with discriminatory DNA profiles for analyzing second- and third-degree relationships.

摘要

我们开发了一种基于新一代测序的新型单核苷酸多态性(SNP)基因分型方法用于二级和三级亲属关系分析,并使用一组引物(A组)和两组引物(A组和B组)设计了1144个SNP和2045个SNP的检测板。在120名日本个体中对这些SNP位点进行了分析,并计算了亲属关系判别似然比(LR)以评估模拟分析中SNP位点数目的影响。似然评估使用来自两个个体(即未知个体和一个参考亲属)的DNA图谱进行。1144个和2045个SNP的基因分型有助于区分姑侄/舅甥等二级亲属和无关个体对。在三级亲属关系分析中,即使在2045个SNP基因分型中,未知个体与一级表亲(FC)之间的对数LR分布也与无关个体的分布没有分开。为了增强对三级亲属关系的判别,我们还评估了来自三个个体(即未知个体和两个一级表亲(2FC))的DNA图谱的有效性。使用2FC对2045个SNP进行似然评估比使用FC更有用。我们的方法应用于12个二级和三级亲属关系分析的亲属案例,1144个和2045个SNP基因型的LR明显高于传统短串联重复序列图谱的LR。此外,我们将2045个SNP在使用有限或降解DNA时的性能与使用大量DNA时的性能进行了比较。使用0.1 ng未降解DNA时,平均一致性高于97%。在对严重降解DNA(降解指数=32.2)的分析中,与21个短串联重复序列图谱的较低一致性率(52.4%)相比,我们从2045个SNP基因型中也检测到了较高的一致性(85.5%)。我们的方法对于分析二级和三级亲属关系的具有鉴别力的DNA图谱应该具有高度敏感性。

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