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通过同时对两种等位基因状态进行实时PCR定量来表征线粒体DNA单核苷酸多态性分型及混合比例评估。

Characterization of mtDNA SNP typing and mixture ratio assessment with simultaneous real-time PCR quantification of both allelic states.

作者信息

Niederstätter Harald, Coble Michael D, Grubwieser Petra, Parsons Thomas J, Parson Walther

机构信息

Institute of Legal Medicine, Innsbruck Medical University, Müllerstrasse 44, 6020, Innsbruck, Austria.

出版信息

Int J Legal Med. 2006 Jan;120(1):18-23. doi: 10.1007/s00414-005-0024-3. Epub 2005 Aug 9.

Abstract

We performed a study on the forensic utility of allele-discriminatory quantitative real-time PCR (rtPCR) using Minor Groove Binder TaqMan probes, targeting the highly variable mitochondrial single nucleotide polymorphism 16519T/C. The apparent single-cycle PCR efficiency was virtually 100% for both 16519 alleles. The allele designations made by rtPCR were concordant with the results obtained in a previous study by sequencing analysis. In heteroplasmic samples, minor allele proportions down to 9% were unambiguously detected and quantified. The variation in allele proportion estimates was essentially the same within and between different rtPCR runs, and the differences between total copy number estimates found for rerun samples were comparable to those found with non-allele-discriminatory quantitative rtPCR assays.

摘要

我们开展了一项研究,使用小沟结合TaqMan探针进行等位基因鉴别定量实时PCR(rtPCR),以高度可变的线粒体单核苷酸多态性16519T/C为靶点,评估其在法医鉴定中的效用。对于16519的两个等位基因,表观单循环PCR效率实际上均为100%。rtPCR得出的等位基因分型结果与先前测序分析研究的结果一致。在异质性样本中,低至9%的次要等位基因比例可被明确检测和定量。不同rtPCR检测批次内和批次间等位基因比例估计值的差异基本相同,重复检测样本的总拷贝数估计值差异与非等位基因鉴别定量rtPCR检测的差异相当。

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