Classical and Non-Classical HLA Alleles as Supplementary Markers in Indirect Kinship Parentage Testing

D. Kouniaki, A. Tsirogianni
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引用次数: 4

Abstract

A civil paternity investigation involving the parents of the deceased alleged father in order to establish a family relationship is presented. On the basis of the 23 autosomal short tandem repeat (aSTR) genotyping results, conclusive proof of paternity was not achieved, as the probability of paternity (W) was calculated to 0.99988. Additional genetic data of 17 classical and non-classical human leukocyte alleles (HLA) typing by next-generation sequencing (NGS) at a high-resolution level supported the hypothesis of grandpaternity over the hypothesis of coincidental paternal obligate allele (POA) sharing (total WaSTR&HLA = 0.9999998). The present study demonstrates the utility of 17 HLA genetic markers-typing in the solution of deficiency cases of disputed parentage.
经典和非经典HLA等位基因作为间接亲缘关系亲子鉴定的补充标记
提出了一项涉及已故据称父亲的父母的民事亲子调查,以建立家庭关系。根据23例常染色体短串联重复序列(aSTR)基因分型结果,未获得父权的确凿证据,父权的概率(W)计算为0.99988。通过下一代测序(NGS)在高分辨率水平上对17个经典和非经典人类白细胞等位基因(HLA)分型的额外遗传数据支持祖父性假说,而不是巧合父性专性等位基因(POA)共享假说(总wastr和HLA = 0.9999998)。本研究证明了17种HLA遗传标记分型在解决有争议的亲子关系缺陷病例中的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Immuno-Analyse & Biologie Specialisee
Immuno-Analyse & Biologie Specialisee 医学-医学实验技术
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6-12 weeks
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