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Data processing, analysis method of gene expression data to identify endogenous reference genes

机译:数据处理,基因表达数据分析方法以鉴定内源参考基因

摘要

Disclosed are data processing and analysis methods for gene expression data for identifying endogenous reference genes and a composition for the quantitative analysis of gene expression, comprising a pair of primers and/or probes useful in amplifying the identified endogenous reference genes. Introduced with the concepts of “Zero's proportion” and CV, the method allows different datasets to be integrally analyzed, thereby searching for novel reference genes. By the method, 2,087 genes are first found as housekeeping genes which are expressed in most tissues, and the usefulness thereof in the relative quantification of different target genes is determined by analyzing their expression stability. Of the 2,087 genes, 13 genes show higher expression stability with lower expression levels across a wide range of samples than traditional reference genes such as GAPDH and ACTS, and therefore are suitable for the normalization of universal genes having relatively low expression levels.
机译:公开了用于鉴定内源参考基因的基因表达数据的数据处理和分析方法以及用于基因表达定量分析的组合物,其包括一对用于扩增鉴定的内源参考基因的引物和/或探针。通过引入“零比例”和CV概念,该方法可以对不同的数据集进行整体分析,从而寻找新的参考基因。通过该方法,首先发现2,087个基因作为在大多数组织中表达的看家基因,并且通过分析它们的表达稳定性来确定其在不同靶基因的相对定量中的有用性。在2,087个基因中,有13个基因在较大范围的样品中显示出更高的表达稳定性,且表达水平低于传统参考基因(例如GAPDH和ACTS),因此适用于表达水平相对较低的通用基因的标准化。

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