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Integrative analysis of genome-scale data by using pseudoinverse projection predicts novel correlation between DNA replication and RNA transcription

机译:通过使用拟逆投影对基因组规模数据进行的综合分析预测了DNA复制与RNA转录之间的新型关联

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摘要

We describe an integrative data-driven mathematical framework that formulates any number of genome-scale molecular biological data sets in terms of one chosen set of data samples, or of profiles extracted mathematically from data samples, designated the “basis” set. By using pseudoinverse projection, the molecular biological profiles of the data samples are least-squares-approximated as superpositions of the basis profiles. Reconstruction of the data in the basis simulates experimental observation of only the cellular states manifest in the data that correspond to those of the basis. Classification of the data samples according to their reconstruction in the basis, rather than their overall measured profiles, maps the cellular states of the data onto those of the basis and gives a global picture of the correlations and possibly also causal coordination of these two sets of states. We illustrate this framework with an integration of yeast genome-scale proteins' DNA-binding data with cell cycle mRNA expression time course data. Novel correlation between DNA replication initiation and RNA transcription during the yeast cell cycle, which might be due to a previously unknown mechanism of regulation, is predicted.
机译:我们描述了一个集成的数据驱动的数学框架,该框架根据一组选定的数据样本或从数据样本中数学提取的配置文件(称为“基础”集)来制定任何数量的基因组规模分子生物学数据集。通过使用伪逆投影,数据样本的分子生物学概况被最小二乘近似为基本概况的叠加。基础中数据的重建模拟了实验中仅观察到数据中对应于基础状态的细胞状态。根据数据样本在其基础上的重构而不是在其总体测量的轮廓上进行分类,将数据的细胞状态映射到基础的那些状态,并给出相关性的全局图以及这两组数据的因果协调状态。我们通过酵母基因组规模蛋白的DNA结合数据与细胞周期mRNA表达时程数据的整合来说明该框架。预测在酵母细胞周期中DNA复制起始和RNA转录之间存在新的相关性,这可能是由于以前未知的调控机制所致。

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