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Quantitative noise analysis for gene expression microarray experiments

机译:基因表达微阵列实验的定量噪声分析

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A major challenge in DNA microarray analysis is to effectively dissociate actual gene expression values from experimental noise. We report here a detailed noise analysis for oligonuleotide-based microarray experiments involving reverse transcription, generation of labeled cRNA (target) through in vitro transcription, and hybridization of the target to the probe immobilized on the substrate. By designing sets of replicate experiments that bifurcate at different steps of the assay, we are able to separate the noise caused by sample preparation and the hybridization processes. We quantitatively characterize the strength of these different sources of noise and their respective dependence on the gene expression level. We find that the sample preparation noise is small, implying that the amplification process during the sample preparation is relatively accurate. The hybridization noise is found to have very strong dependence on the expression level, with different characteristics for the low and high expression values. The hybridization noise characteristics at the high expression regime are mostly Poisson-like, whereas its characteristics for the small expression levels are more complex, probably due to cross-hybridization. A method to evaluate the significance of gene expression fold changes based on noise characteristics is proposed.
机译:DNA微阵列分析中的主要挑战是如何有效地将实际基因表达值与实验噪声区分开。我们在这里报告了基于寡核苷酸的微阵列实验的详细噪声分析,该实验涉及逆转录,通过体外转录生成标记的cRNA(靶标)以及将靶标与固定在基质上的探针杂交。通过设计在实验的不同步骤分叉的重复实验集,我们能够分离出样品制备和杂交过程所产生的噪音。我们定量地表征了这些不同噪声源的强度及其对基因表达水平的依赖性。我们发现样品制备噪声很小,这意味着样品制备过程中的扩增过程相对准确。发现杂交噪声对表达水平有非常强的依赖性,对于低和高表达值具有不同的特性。高表达模式下的杂交噪声特征大多为泊松样,而小表达水平下的杂交噪声特征则更为复杂,这可能是由于交叉杂交所致。提出了一种基于噪声特征评价基因表达倍数变化意义的方法。

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