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首页> 外文期刊>International Journal of Legal Medicine >Comprehensive mutation analysis of 17 Y-chromosomal short tandem repeat polymorphisms included in the AmpFlSTR® Yfiler® PCR amplification kit
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Comprehensive mutation analysis of 17 Y-chromosomal short tandem repeat polymorphisms included in the AmpFlSTR® Yfiler® PCR amplification kit

机译:AmpFlSTR®Yfiler®PCR扩增试剂盒中包含的17个Y染色体短串联重复序列多态性的全面突变分析

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摘要

The Y-chromosomal short tandem repeat (Y-STR) polymorphisms included in the AmpFlSTR® Yfiler® polymerase chain reaction amplification kit have become widely used for forensic and evolutionary applications where a reliable knowledge on mutation properties is necessary for correct data interpretation. Therefore, we investigated the 17 Yfiler Y-STRs in 1,730–1,764 DNA-confirmed father–son pairs per locus and found 84 sequence-confirmed mutations among the 29,792 meiotic transfers covered. Of the 84 mutations, 83 (98.8%) were single-repeat changes and one (1.2%) was a double-repeat change (ratio, 1:0.01), as well as 43 (51.2%) were repeat gains and 41 (48.8%) repeat losses (ratio, 1:0.95). Medians from Bayesian estimation of locus-specific mutation rates ranged from 0.0003 for DYS448 to 0.0074 for DYS458, with a median rate across all 17 Y-STRs of 0.0025. The mean age (at the time of son’s birth) of fathers with mutations was with 34.40 (±11.63) years higher than that of fathers without ones at 30.32 (±10.22) years, a difference that is highly statistically significant (p 1%, 12 had mutation rates of >0.1% and four of <0.1%, (2) single-repeat changes were strongly favored over multiple-repeat ones for all loci but 1 and (3) considerable variation existed among loci in the ratio of repeat gains versus losses. Our finding of three Y-STR mutations in one father–son pair (and two pairs with two mutations each) has consequences for determining the threshold of allelic differences to conclude exclusion constellations in future applications of Y-STRs in paternity testing and pedigree analyses.
机译:AmpFlSTR®Yfiler®聚合酶链反应扩增试剂盒中包含的Y染色体短串联重复序列(Y-STR)多态性已广泛用于法医学和进化应用,在这些应用中,对于突变特性的可靠知识对于正确的数据解释必不可少。因此,我们研究了每个基因座中1,730–1,764个DNA确认的父子对中的17个Yfiler Y-STR,发现了29,792个减数分裂转移中的84个序列确认的突变。在这84个突变中,有83个(98.8%)是单重复改变,一个(1.2%)是双重复改变(比例为1:0.01),还有43个(51.2%)是重复获得,有41个(48.8) %)重复损失(比例为1:0.95)。根据贝叶斯估计,基因座特异性突变率的中位数范围从DYS448的0.0003到DYS458的0.0074,所有17个Y-STR的中位数为0.0025。具有突变的父亲的平均年龄(在儿子出生时)比没有父亲的父亲的平均年龄高30.32(±10.22)岁,高34.40(±11.63)岁,这一差异具有统计学意义(p 1%, 12个突变率> 0.1%,四个突变率<0.1%,(2)对于所有基因座,单重复变化都比多重复变化更受青睐,但是1和(3)基因座之间的重复增益比例存在相当大的差异我们发现一对父子对中的三个Y-STR突变(以及两个父对,每个都有两个突变)对确定等位基因差异的阈值具有重要意义,从而可以推断出将Y-STR应用于未来的亲子鉴定和鉴定。谱系分析。

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