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Identification of dual false indirect exclusions on the D5S818 and FGA loci.

机译:鉴定D5S818和FGA基因座上的双重假间接排斥。

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Here, we present a case in which the result of a maternity test was obscured due to two false indirect exclusions that occurred in two out of 15 genetic loci through the use of the AmpFlSTR Identifiler PCR Amplification kit (Applied Biosystems, Foster City, CA). The Identifiler kit failed to amplify allele 11 of the D5S818 system on the child and failed to capture the existence of allele 13 on the FGA system on both mother and child. The situation was remedied through use of the PowerPlex 16 PCR Amplification Kit (Promega, Madison, WI) which used different primers with a different allele range than that of the Identifiler kit. Maternity was confirmed through sequencing and it was found that the failure of the Identifiler kit to amplify allele 11 on the D5S818 system was the result of an incompatibility to the primer-binding site due to a mutation that changed a guanine (G) into a thymine (T) 55 base pairs (bp) downstream of the repeat. The inability of the Identifiler kit to pick up allele 13 of the FGA system was due to the out-of-range location of the allele. Indirect exclusions can be misleading if they are not fully investigated since allele range as well as primer-binding affinity are two confounders that must be addressed to ensure accuracy of the test results.
机译:在这里,我们介绍了一个案例,其中由于使用AmpFlSTR标识符PCR扩增试剂盒(Applied Biosystems,福斯特城,加利福尼亚州)而在15个基因位点中有两个发生了两个错误的间接排除,导致产妇检查结果模糊不清。 Identifiler试剂盒无法在儿童上扩增D5S818系统的等位基因11,也无法捕获母子FGA系统上等位基因13的存在。通过使用PowerPlex 16 PCR扩增试剂盒(Promega,麦迪逊,威斯康星州)纠正了这种情况,该试剂盒使用了与Identifiler试剂盒不同等位基因范围的不同引物。通过测序确认了产妇,发现Identifiler试剂盒未能扩增D5S818系统上的等位基因11是由于将鸟嘌呤(G)变为胸腺嘧啶的突变导致引物结合位点不兼容的结果(T)重复序列下游的55个碱基对(bp)。 Identifiler试剂盒无法提取FGA系统的等位基因13是由于等位基因的位置超出范围。如果对等位基因范围以及引物结合亲和力是两个混杂因素,必须加以解决以确保测试结果的准确性,但如果不对它们进行全面研究,则可能会误导间接排斥。

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