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Human and mouse oligonucleotide-based array CGH

机译:基于人和小鼠寡核苷酸的阵列CGH

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摘要

Array-based comparative genomic hybridization is a high resolution method for measuring chromosomal copy number changes. Here we present a validated protocol using in-house spotted oligonucleotide libraries for array comparative genomic hybridization (CGH). This oligo array CGH platform yields reproducible results and is capable of detecting single copy gains, multi-copy amplifications as well as homozygous and heterozygous deletions as small as 100 kb with high resolution. A human oligonucleotide library was printed on amine binding slides. Arrays were hybridized using a hybstation and analysed using BlueFuse feature extraction software, with > 95% of spots passing quality control. The protocol allows as little as 300 ng of input DNA and a 90% reduction of Cot-1 DNA without compromising quality. High quality results have also been obtained with DNA from archival tissue. Finally, in addition to human oligo arrays, we have applied the protocol successfully to mouse oligo arrays. We believe that this oligo-based platform using 'off-the-shelf' oligo libraries provides an easy accessible alternative to BAC arrays for CGH, which is cost-effective, available at high resolution and easily implemented for any sequenced organism without compromising the quality of the results.
机译:基于阵列的比较基因组杂交是一种用于测量染色体拷贝数变化的高分辨率方法。在这里,我们提出了使用内部斑点寡核苷酸文库进行阵列比较基因组杂交(CGH)的验证协议。该寡核苷酸阵列CGH平台可产生可重复的结果,并且能够以高分辨率检测小至100 kb的单拷贝增益,多拷贝扩增以及纯合和杂合缺失。将人寡核苷酸文库印刷在胺结合载玻片上。使用杂交仪杂交阵列,并使用BlueFuse特征提取软件进行分析,> 95%的斑点通过了质量控制。该协议允许在不影响质量的情况下,输入DNA仅为300 ng,Cot-1 DNA减少90%。来自档案组织的DNA也获得了高质量的结果。最后,除了人类寡核苷酸阵列,我们还成功地将该协议应用于了小鼠寡核苷酸阵列。我们相信,这种基于寡核苷酸的平台使用“现成的”寡核苷酸库,为CGH的BAC阵列提供了一种易于访问的替代方案,它具有成本效益,可提供高分辨率且可轻松用于任何测序生物,而不会影响质量结果。

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