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An experimental loop design for the detection of constitutional chromosomal aberrations by array CGH

机译:利用阵列CGH检测结构染色体畸变的实验环路设计

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摘要

BackgroundComparative genomic hybridization microarrays for the detection of constitutional chromosomal aberrations is the application of microarray technology coming fastest into routine clinical application. Through genotype-phenotype association, it is also an important technique towards the discovery of disease causing genes and genomewide functional annotation in human. When using a two-channel microarray of genomic DNA probes for array CGH, the basic setup consists in hybridizing a patient against a normal reference sample. Two major disadvantages of this setup are (1) the use of half of the resources to measure a (little informative) reference sample and (2) the possibility that deviating signals are caused by benign copy number variation in the "normal" reference instead of a patient aberration. Instead, we apply an experimental loop design that compares three patients in three hybridizations.
机译:背景技术用于检测体质性染色体畸变的比较基因组杂交微阵列是微阵列技术的应用,是常规临床应用中最快的。通过基因型-表型的关联,它也是发现人类致病基因和全基因组功能注释的重要技术。将基因组DNA探针的两通道微阵列用于CGH阵列时,基本设置包括将患者与正常参考样品杂交。此设置的两个主要缺点是(1)使用一半的资源来测量(少量信息)参考样本,以及(2)偏差信号是由“正常”参考中的良性拷贝数变化引起的,而不是病人的畸变。取而代之的是,我们采用了实验环设计,可以比较三种杂交中的三名患者。

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