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New sequence variants detected at DXS10148, DXS10074 and DXS10134 loci

机译:在DXS10148,DXS10074和DXS10134位点检测到新的序列变体

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A great amount of population and forensic genetic data are available for X-STRs supporting the need for having a common and accurate nomenclature among laboratories allowing for better communication, data exchange, and data comparison. DXS10148, DXS10074 and DXS10134 are commonly used X-STRs particularly due to their inclusion in the commercial kit Investigator Argus X-12 (Qiagen). Samples from West Africa and Iraq were sequenced for all three X-STRs allowing the detection of new DNA sequence variants. At DXS10148, variation was detected at four bases downstream from the flanking region from the repeat motif. The sequence AAGG-AAAG has been detected for the first time as a varying (AAGG-AAAG)(1-3) motif, in the present work. One additional string when compared to the common one (AAGG-AAAG)(2) adds eight bases to the fragment size of the tetranucleotide STR. This means that 2 repeats are added in these cases to the fragment size of the allele, while the presence of only one copy will reduce the expected allele size by 2 repeats. At DXS10074 two varying stretches consisting of AC and AG dinucleotide repeats were observed in the upstream flanking region, six bases from the main repeat core that also influence the expected allele size. DXS10134 revealed a simpler nomenclature in the Guinea-Bissau sample set when compared to the previously described allele nomenclature. This detected new hidden variation also has impact on the actual allele nomenclature at this locus as it contributes to a new class of short alleles so far undetected in other studies. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
机译:X-STR提供了大量的人口和法医遗传数据,支持实验室之间具有通用且准确的命名法,以便更好地进行交流,数据交换和数据比较。 DXS10148,DXS10074和DXS10134是常用的X-STR,特别是因为它们包含在商业套件Investigator Argus X-12(Qiagen)中。对来自西非和伊拉克的所有三个X-STR进行测序,从而可以检测新的DNA序列变体。在DXS10148处,在重复基序侧翼区域下游的四个碱基处检测到变异。在本工作中,序列AAGG-AAAG首次被检测为(AAGG-AAAG)(1-3)变体。与普通的(AAGG-AAAG)(2)相比,另外一个字符串为四核苷酸STR的片段大小增加了8个碱基。这意味着在这些情况下,等位基因的片段大小会增加2个重复,而只有一个拷贝的存在会使预期的等位基因大小减少2个重复。在DXS10074的上游侧翼区域观察到了两个由AC和AG二核苷酸重复序列组成的可变片段,这些片段来自主重复片段核心的六个碱基也影响了预期的等位基因大小。与先前描述的等位基因命名法相比,DXS10134在几内亚比绍的样本集中揭示了一个更简单的命名法。这种检测到的新的隐藏变异也对该位点的实际等位基因命名有影响,因为它促成了迄今为止在其他研究中未发现的一类新的短等位基因。 (C)2015 Elsevier Ireland Ltd.保留所有权利。

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