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Predicting Causal Relationships from Biological Data: Applying Automated Casual Discovery on Mass Cytometry Data of Human Immune Cells

机译:从生物学数据预测因果关系:在人类免疫细胞的质量细胞数据上应用自动偶然发现

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摘要

Learning the causal relationships that define a molecular system allows us to predict how the system will respond to different interventions. Distinguishing causality from mere association typically requires randomized experiments. Methods for automated causal discovery from limited experiments exist, but have so far rarely been tested in systems biology applications. In this work, we apply state-of-the art causal discovery methods on a large collection of public mass cytometry data sets, measuring intra-cellular signaling proteins of the human immune system and their response to several perturbations. We show how different experimental conditions can be used to facilitate causal discovery, and apply two fundamental methods that produce context-specific causal predictions. Causal predictions were reproducible across independent data sets from two different studies, but often disagree with the KEGG pathway databases. Within this context, we discuss the caveats we need to overcome for automated causal discovery to become a part of the routine data analysis in systems biology.
机译:学习定义分子系统的因果关系可以使我们预测系统如何响应不同的干预措施。区分因果关系和单纯关联通常需要随机实验。存在从有限的实验中自动发现因果的方法,但是到目前为止,很少在系统生物学应用中进行过测试。在这项工作中,我们将最新的因果发现方法应用到大量公共质量细胞数据集上,以测量人类免疫系统的细胞内信号蛋白及其对几种干扰的反应。我们展示了如何使用不同的实验条件促进因果关系发现,并应用两种基本方法来产生因果而异的因果关系预测。因果关系预测可以在来自两个不同研究的独立数据集之间重现,但常常与KEGG通路数据库不同。在这种情况下,我们讨论了自动因果发现要成为系统生物学常规数据分析的一部分时需要克服的警告。

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