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A method for accurate detection of genomic microdeletions using real-time quantitative PCR

机译:一种使用实时定量PCR准确检测基因组微缺失的方法

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摘要

BackgroundQuantitative Polymerase Chain Reaction (qPCR) is a well-established method for quantifying levels of gene expression, but has not been routinely applied to the detection of constitutional copy number alterations of human genomic DNA. Microdeletions or microduplications of the human genome are associated with a variety of genetic disorders. Although, clinical laboratories routinely use fluorescence in situ hybridization (FISH) to identify such cryptic genomic alterations, there remains a significant number of individuals in which constitutional genomic imbalance is suspected, based on clinical parameters, but cannot be readily detected using current cytogenetic techniques.
机译:背景技术定量聚合酶链反应(qPCR)是定量基因表达水平的公认方法,但尚未常规应用于检测人类基因组DNA的构成拷贝数变化。人类基因组的微缺失或微复制与多种遗传疾病有关。尽管临床实验室常规使用荧光原位杂交(FISH)来识别这种隐秘的基因组改变,但根据临床参数,仍有相当多的人怀疑其构成基因组不平衡,但不能使用当前的细胞遗传学技术轻易检测到。

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