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A semi-parametric statistical model for integrating gene expression profiles across different platforms

机译:一种半导体统计模型,用于在不同平台上积分基因表达谱

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Background: Determining differentially expressed genes (DEGs) between biological samples is the key to understand how genotype gives rise to phenotype. RNA-seq and microarray are two main technologies for profiling gene expression levels. However, considerable discrepancy has been found between DEGs detected using the two technologies. Integration data across these two platforms has the potential to improve the power and reliability of DEG detection.Methods: We propose a rank-based semi-parametric model to determine DEGs using information across different sources and apply it to the integration of RNA-seq and microarray data. By incorporating both the significance of differential expression and theconsistency across platforms, our method effectively detects DEGs with moderate but consistent signals. We demonstrate the effectiveness of our method using simulation studies, MAQC/SEQC data and a synthetic microRNA dataset.Conclusion's: Our integration method is not only robust to noise and heterogeneity in the data, bgt also adaptive to the structure of data. In our simulations and real data studies, our approach shows a higher discriminate power and identifies more biologically relevant DEGs than eBayes, DEseq and some commonly used meta-analysis methods.
机译:背景:在生物样品之间确定差异表达的基因(DEGS)是了解基因型如何产生表型的关键。 RNA-SEQ和微阵列是分析基因表达水平的两个主要技术。然而,使用两种技术检测到的DEG之间已经发现了相当大的差异。这两个平台上的集成数据具有提高DEG检测的功率和​​可靠性。微阵列数据。通过纳入差异表达和跨平台的差异性的意义,我们的方法有效地检测了中等但一致的信号的DEG。我们展示了使用仿真研究,MAQC / SEQC数据和合成MicroRNA数据集的方法的有效性。结论:我们的集成方法不仅稳健地对数据中的噪声和异质性,BGT也适用于数据的结构。在我们的模拟和真实数据研究中,我们的方法显示了更高的鉴别力,并识别比eBayes,DESEQ和一些常用的META分析方法更高的生物相关的次数。

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