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BAC to the future! or oligonucleotides: a perspective for micro array comparative genomic hybridization (array CGH)

机译:BAC走向未来!或寡核苷酸:微阵列比较基因组杂交的前景(阵列CGH)

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摘要

The array CGH technique (Array Comparative Genome Hybridization) has been developed to detect chromosomal copy number changes on a genome-wide and/or high-resolution scale. It is used in human genetics and oncology, with great promise for clinical application. Until recently primarily PCR amplified bacterial artificial chromosomes (BACs) or cDNAs have been spotted as elements on the array. The large-scale DNA isolations or PCR amplifications of the large-insert clones necessary for manufacturing the arrays are elaborate and time-consuming. Lack of a high-resolution highly sensitive (commercial) alternative has undoubtedly hindered the implementation of array CGH in research and diagnostics. Recently, synthetic oligonucleotides as arrayed elements have been introduced as an alternative substrate for array CGH, both by academic institutions as well as by commercial providers. Oligonucleotide libraries or ready-made arrays can be bought off-the-shelf saving considerable time and efforts. For RNA expression profiling, we have seen a gradual transition from in-house printed cDNA-based expression arrays to oligonucleotide arrays and we expect a similar transition for array CGH. This review compares the different platforms and will attempt to shine a light on the ‘BAC to the future’ of the array CGH technique.
机译:已经开发了阵列CGH技术(阵列比较基因组杂交)以检测全基因组范围和/或高分辨率范围内的染色体拷贝数变化。它被用于人类遗传学和肿瘤学,具有广阔的临床应用前景。直到最近,主要还是将PCR扩增的细菌人工染色体(BAC)或cDNA定位为阵列上的元件。制造阵列所需的大插入克隆的大规模DNA分离或PCR扩增是复杂且耗时的。高分辨率,高灵敏度(商业)替代方案的缺乏无疑阻碍了阵列CGH在研究和诊断中的实施。近来,学术机构以及商业提供商都已经引入了合成的寡核苷酸作为阵列元件作为阵列CGH的替代底物。可以购买现成的寡核苷酸文库或现成的阵列,从而节省了大量时间和精力。对于RNA表达谱,我们已经看到了从内部基于cDNA的印刷表达阵列到寡核苷酸阵列的逐渐过渡,并且我们期望阵列CGH的过渡类似。这篇评论比较了不同的平台,并将尝试阐明阵列CGH技术的“ BAC走向未来”。

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