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MAP: model-based analysis of proteomic data to detect proteins with significant abundance changes

机译:地图:基于模型的蛋白质组学数据分析,以检测具有显着丰富变化的蛋白质

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Isotope-labeling-based mass spectrometry (MS) is widely used in quantitative proteomic studies. With this technique, the relative abundance of thousands of proteins can be efficiently profiled in parallel, greatly facilitating the detection of proteins differentially expressed across samples. However, this task remains computationally challenging. Here we present a new approach, termed Model-based Analysis of Proteomic data (MAP), for this task. Unlike many existing methods, MAP does not require technical replicates to model technical and systematic errors, and instead utilizes a novel step-by-step regression analysis to directly assess the significance of observed protein abundance changes. We applied MAP to compare the proteomic profiles of undifferentiated and differentiated mouse embryonic stem cells (mESCs), and found it has superior performance compared with existing tools in detecting proteins differentially expressed during mESC differentiation. A web-based application of MAP is provided for online data processing at http://bioinfo.sibs.ac.cn/shaolab/MAP.? The Author(s) 2019.
机译:基于同位素标记的质谱(MS)广泛用于定量蛋白质组学研究。利用这种技术,可以平行地有效地分析成千上万的蛋白质的相对丰度,大大促进了跨越样品差异表达的蛋白质的检测。但是,此任务仍然是计算挑战。在这里,我们提出了一种新的方法,即在此任务中被称为基于模型的蛋白质组学数据(MAP)分析。与许多现有方法不同,地图不需要技术复制来模拟技术和系统误差,而是利用新的逐步回归分析,以直接评估观察到的蛋白质丰度变化的重要性。我们施加地图以比较未分化和分化的小鼠胚胎干细胞(MESCS)的蛋白质组学谱,并发现它具有优异的性能与检测在MESC分化期间差异表达的蛋白质的现有工具相比。提供了基于Web的地图应用,用于网上数据处理http://bioinfo.sibs.ac.cn/shaolab/map。?作者2019年。

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