Suppr超能文献

应用 ForenSeq™ DNA Signature Prep Kit 对秘鲁安第斯东北地区人群进行常染色体 STR 和 SNP 特征分析。

Autosomal STR and SNP characterization of populations from the Northeastern Peruvian Andes with the ForenSeq™ DNA Signature Prep Kit.

机构信息

Department of Forensic Medicine, University of Helsinki, PO Box 40, FI-00014 Helsinki, Finland.

Department of Forensic Medicine, University of Helsinki, PO Box 40, FI-00014 Helsinki, Finland; Forensic Genetics Unit, Finnish Institute for Health and Welfare, PO BOX 30, FI-00271 Helsinki, Finland.

出版信息

Forensic Sci Int Genet. 2021 May;52:102487. doi: 10.1016/j.fsigen.2021.102487. Epub 2021 Feb 23.

Abstract

Autosomal DNA data from Peru for human identity testing purposes are scarce in the scientific literature, which hinders obtaining an appropriate portrait of the genetic variation of the resident populations. In this study we genetically characterize five populations from the Northeastern Peruvian Andes (Chachapoyas, Awajún, Wampís, Huancas and Cajamarca). Autosomal short tandem repeat (aSTR) and identity informative single nucleotide polymorphism (iiSNP) data from a total of 233 unrelated individuals are provided, and forensic genetic parameters are calculated for each population and for the combined set Northeastern Peruvian Andes. After correction for multiple testing in the whole dataset of the Northeastern Peruvian Andes, the only departure from Hardy-Weinberg equilibrium was observed in locus rs2111980. Twenty one out of 27 aSTR loci exhibited an increased number of alleles due to sequence variation in the repeat motif and flanking regions. For iiSNPs 33% of the loci displayed flanking region variation. The combined random match probability (RMP), assuming independence of all loci (aSTRs and iiSNPs), in the Chachapoyas, the population with the largest samples size (N = 172), was 8.14 × 10 for length-based data while for sequence-based was 4.15 × 10. In the merged dataset (Northeastern Peruvian Andes; N = 233), the combined RMP when including all markers were 2.96 × 10 (length-based) and 3.21 × 10 (sequence-based). These new data help to fill up some of the gaps in the genetic canvas of South America and provide essential length- and sequence-based background information for other forensic genetic studies in Peru.

摘要

秘鲁的常染色体 DNA 数据在科学文献中用于人类身份检测的内容很少,这阻碍了对居住人群遗传变异的适当描述。在这项研究中,我们对秘鲁东北部安第斯山脉的五个群体(查查波亚斯、阿瓦朱恩、万皮斯、万卡约斯和卡哈马卡)进行了基因特征分析。提供了来自 233 个无关个体的常染色体短串联重复(aSTR)和身份信息单核苷酸多态性(iiSNP)数据,并为每个群体和整个秘鲁东北部安第斯山脉的组合群体计算了法医遗传学参数。在对整个秘鲁东北部安第斯山脉数据集进行多次测试校正后,仅在 rs2111980 基因座观察到偏离 Hardy-Weinberg 平衡。由于重复基序和侧翼区域的序列变异,27 个 aSTR 基因座中的 21 个基因座显示出等位基因数量增加。对于 iiSNP,33%的基因座显示侧翼区域变异。在 Chachapoyas 群体中,假设所有基因座(aSTR 和 iiSNP)相互独立的随机匹配概率(RMP)最大(N=172),基于长度的数据为 8.14×10,而基于序列的数据为 4.15×10。在合并数据集(秘鲁东北部安第斯山脉;N=233)中,当包括所有标记时,基于长度的联合 RMP 为 2.96×10,基于序列的联合 RMP 为 3.21×10。这些新数据有助于填补南美洲遗传图谱的一些空白,并为秘鲁其他法医遗传学研究提供必要的基于长度和序列的背景信息。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验