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首页> 外文期刊>Genomics >Assessment and integration of publicly available SAGE, cDNA microarray, and oligonucleotide microarray expression data for global coexpression analyses.
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Assessment and integration of publicly available SAGE, cDNA microarray, and oligonucleotide microarray expression data for global coexpression analyses.

机译:评估和整合可公开获得的SAGE,cDNA微阵列和寡核苷酸微阵列表达数据,以进行全局共表达分析。

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摘要

Large amounts of gene expression data from several different technologies are becoming available to the scientific community. A common practice is to use these data to calculate global gene coexpression for validation or integration of other "omic" data. To assess the utility of publicly available datasets for this purpose we have analyzed Homo sapiens data from 1202 cDNA microarray experiments, 242 SAGE libraries, and 667 Affymetrix oligonucleotide microarray experiments. The three datasets compared demonstrate significant but low levels of global concordance (rc<0.11). Assessment against Gene Ontology (GO) revealed that all three platforms identify more coexpressed gene pairs with common biological processes than expected by chance. As the Pearson correlation for a gene pair increased it was more likely to be confirmed by GO. The Affymetrix dataset performed best individually with gene pairs of correlation 0.9-1.0 confirmed by GO in 74% of cases. However, in all cases, gene pairs confirmed by multiple platforms were more likely to be confirmed by GO. We show that combining results from different expression platforms increases reliability of coexpression. A comparison with other recently published coexpression studies found similar results in terms of performance against GO but with each method producing distinctly different gene pair lists.
机译:来自多种不同技术的大量基因表达数据正可供科学界使用。一种常见的做法是使用这些数据来计算全局基因共表达,以验证或整合其他“组学”数据。为了评估用于此目的的公开数据集的实用性,我们分析了来自1202个cDNA微阵列实验,242个SAGE文库和667个Affymetrix寡核苷酸微阵列实验的智人数据。比较的三个数据集显示出显着但较低的全局一致性(rc <0.11)。针对基因本体论(GO)的评估显示,这三个平台都能通过共同的生物学过程识别出更多的共表达基因对,而这并非偶然。随着基因对的皮尔逊相关性增加,GO更有可能证实这一点。在74%的病例中,GO证实Affymetrix数据集与0.9-1.0的相关基因对表现最佳。但是,在所有情况下,由多个平台确认的基因对更有可能由GO确认。我们表明,将来自不同表达平台的结果结合起来可以提高共表达的可靠性。与其他最近发表的共表达研究的比较发现,在抗GO方面的表现相似,但每种方法产生的基因对列表明显不同。

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