高分辨率比较基因组杂交检测PCR扩增的DNA1中7-8兆对缺失

J. Larsen, A. M. Ottesen, M. Kirchhoff, C. Lundsteen, J. Larsen
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引用次数: 7

摘要

我们研究了与使用未扩增的DNA相比,使用退化寡核苷酸引物PCR (DOP‐PCR)扩增的DNA是否可以检测到比较基因组杂交分析的空间分辨率变化。用DOP - PCR扩增了5例11q缺失的B细胞白血病DNA样本,并用高分辨率比较基因组杂交(HR - CGH)进行分析,以评估畸变大小的检测限。通过HR - CGH,我们发现DOP - PCR CGH对缺失的检出限在3 Mbp到7-8 Mbp之间。
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High Resolution Comparative Genomic Hybridization Detects 7–8 Megabasepair Deletion in PCR Amplified DNA1
We investigated if any change in spatial resolution of comparative genomic hybridization analysis could be detected when using DNA amplified by degenerate oligonucleotide primed PCR (DOP‐PCR) as opposed to the use of unamplified DNA. Five DNA samples from B‐cell leukemias with small 11q deletions were amplified by DOP‐PCR and analysed by means of high resolution comparative genomic hybridization (HR‐CGH) for the evaluation of aberration size detection limit. By means of HR‐CGH, we found the detection limit of DOP‐PCR CGH for deletions to be between 3 Mbp and 7–8 Mbp.
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