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Estimating the proportion of microarray probes expressed in an RNA sample.

机译:估计在RNA样品中表达的微阵列探针的比例。

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摘要

A fundamental question in microarray analysis is the estimation of the number of expressed probes in different RNA samples. Negative control probes available in the latest microarray platforms, such as Illumina whole genome expression BeadChips, provide a unique opportunity to estimate the number of expressed probes without setting a threshold. A novel algorithm was proposed in this study to estimate the number of expressed probes in an RNA sample by utilizing these negative controls to measure background noise. The performance of the algorithm was demonstrated by comparing different generations of Illumina BeadChips, comparing the set of probes targeting well-characterized RefSeq NM transcripts with other probes on the array and comparing pure samples with heterogenous samples. Furthermore, hematopoietic stem cells were found to have a larger transcriptome than progenitor cells. Aire knockout medullary thymic epithelial cells were shown to have significantly less expressed probes than matched wild-type cells.
机译:微阵列分析中的一个基本问题是估计不同RNA样品中表达探针的数量。最新的微阵列平台中可用的阴性对照探针,例如Illumina全基因组表达BeadChips,提供了一个独特的机会来估计表达探针的数量而无需设置阈值。在这项研究中提出了一种新的算法,通过利用这些阴性对照来测量背景噪声来估计RNA样品中表达的探针数量。通过比较不同代的Illumina BeadChips,将针对特征明确的RefSeq NM转录本的探针组与阵列上的其他探针进行比较,并将纯样品与异质样品进行比较,证明了算法的性能。此外,发现造血干细胞比祖细胞具有更大的转录组。已显示,Aire敲除髓样胸腺上皮细胞的探针表达明显低于匹配的野生型细胞。

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