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Assessment of the sensitivity and specificity of oligonucleotide (50mer) microarrays

机译:寡核苷酸(50mer)微阵列的敏感性和特异性评估

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To examine the utility and performance of 50mer oligonucleotide (oligonucleotide probe) microarrays, gene-specific oligonucleotide probes were spotted along with PCR probes onto glass microarrays and the performance of each probe type was evaluated. The specificity of oligonucleotide probes was studied using target RNAs that shared various degrees of sequence similarity. Sensitivity was defined as the ability to detect a 3-fold change in mRNA. No significant difference in sensitivity between oligonucleotide probes and PCR probes was observed and both had a minimum reproducible detection limit of approx 10 mRNA copies/cell. Specificity studies showed that for a given oligonucleotide probe any 'non-target' transcripts (cDNAs) >75% similar over the 50 base target may show cross-hybridization. Thus non-target sequences which have >75%-80% sequence similarity with target sequences (within the oligonucleotide probe 50 base target region) will contribute to the overall signal intensity. In addition, if the 50 base target region is marginally similar, it must not include a stretch of complementary sequence >15 contiguous bases. Therefore, knowledge about the target sequence, as well as its similarity to other mRNAs in the target tissue or RNA sample, is required to design successful oligonucleotide probes for quality microarray results. Together these results validate that utility of oligonucleotide probe (50mer) glass micro-arrays.
机译:为了检查50mer寡核苷酸(寡核苷酸探针)微阵列的效用和性能,将基因特异性寡核苷酸探针与PCR探针一起点到玻璃微阵列上,并评估每种探针类型的性能。使用共享各种程度的序列相似性的靶RNA研究了寡核苷酸探针的特异性。灵敏度定义为检测mRNA 3倍变化的能力。在寡核苷酸探针和PCR探针之间没有观察到灵敏度的显着差异,并且两者的最小可重复检测极限均为约10个mRNA拷贝/细胞。特异性研究表明,对于给定的寡核苷酸探针,在50个碱基的靶标上> 75%相似的任何“非靶标”转录本(cDNA)都可能显示交叉杂交。因此,与靶序列具有> 75%-80%序列相似性的非靶序列(在寡核苷酸探针50个碱基靶区域内)将有助于总体信号强度。此外,如果50个碱基的目标区域略微相似,则它不得包含一段大于15个连续碱基的互补序列。因此,需要有关靶序列及其与靶组织或RNA样品中其他mRNA相似性的知识,以设计出成功的寡核苷酸探针,以得到高质量的微阵列结果。这些结果共同证明了寡核苷酸探针(50mer)玻璃微​​阵列的实用性。

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