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首页> 外文期刊>Combinatorial Chemistry & High Throughput Screening >Oligonucleotide Fingerprinting of Arrayed Genomic DNA Sequences Using LNA-Modified Hybridization Probes
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Oligonucleotide Fingerprinting of Arrayed Genomic DNA Sequences Using LNA-Modified Hybridization Probes

机译:使用LNA修饰的杂交探针的基因组DNA序列的寡核苷酸指纹图谱。

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Recently, we established a robust method for the detection of hybridization events using a DNA microarray deposited on a nanoporous membrane. Here, in a follow-up study, we demonstrate the performance of this approach on a larger set of LNA-modified oligoprobes and genomic DNA sequences. Twenty-six different LNA-modified 7-mer oligoprobes were hybridized to a set of 66 randomly selected human genomic DNA clones spotted on a nanoporous membrane slide. Subsequently, assay sensitivity analysis was performed using receiver operating characteristic (ROC) curves. Comparison of LNA-modified heptamers and DNA heptamers revealed that the LNA modification clearly improved sensitivity and specificity of hybridization experiment. Clustering analysis was applied in order to test practical performance of hybridization experiments with LNA-modified oligoprobes in recognizing similarity of genomic DNA sequences. Comparing the results with the theoretical sequence clusters, we conclude that the application of LNA-modified oligoprobes allows for reliable clustering of DNA sequences which reflects the underlying sequence homology. Our results show that LNA-modified oligoprobes can be used effectively to unravel sequence similarity of DNA sequences and thus, to characterize the content of unknown DNA libraries.
机译:最近,我们建立了一种使用沉积在纳米多孔膜上的DNA微阵列检测杂交事件的可靠方法。在这里,在后续研究中,我们证明了该方法在较大的一组LNA修饰的寡核苷酸探针和基因组DNA序列上的性能。将二十六个不同的LNA修饰的7-mer寡聚探针与点在纳米多孔膜载玻片上的66个随机选择的人类基因组DNA克隆进行杂交。随后,使用接收器工作特性(ROC)曲线进行测定灵敏度分析。对LNA修饰的七聚体和DNA七聚体的比较表明,LNA修饰明显提高了杂交实验的敏感性和特异性。进行聚类分析是为了测试与LNA修饰的寡核苷酸杂交实验在识别基因组DNA序列相似性方面的实际性能。将结果与理论序列簇进行比较,我们得出的结论是,应用LNA修饰的寡核苷酸探针可以可靠地聚集DNA序列,从而反映出潜在的序列同源性。我们的结果表明,LNA修饰的寡核苷酸可以有效地用于揭示DNA序列的序列相似性,从而表征未知DNA库的内容。

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