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首页> 外文期刊>BMC Bioinformatics >Visualizing complex feature interactions and feature sharing in genomic deep neural networks
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Visualizing complex feature interactions and feature sharing in genomic deep neural networks

机译:在基因组深度神经网络中可视化复杂的特征交互和特征共享

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Visualization tools for deep learning models typically focus on discovering key input features without considering how such low level features are combined in intermediate layers to make decisions. Moreover, many of these methods examine a network’s response to specific input examples that may be insufficient to reveal the complexity of model decision making. We present DeepResolve, an analysis framework for deep convolutional models of genome function that visualizes how input features contribute individually and combinatorially to network decisions. Unlike other methods, DeepResolve does not depend upon the analysis of a predefined set of inputs. Rather, it uses gradient ascent to stochastically explore intermediate feature maps to 1) discover important features, 2) visualize their contribution and interaction patterns, and 3) analyze feature sharing across tasks that suggests shared biological mechanism. We demonstrate the visualization of decision making using our proposed method on deep neural networks trained on both experimental and synthetic data. DeepResolve is competitive with existing visualization tools in discovering key sequence features, and identifies certain negative features and non-additive feature interactions that are not easily observed with existing tools. It also recovers similarities between poorly correlated classes which are not observed by traditional methods. DeepResolve reveals that DeepSEA’s learned decision structure is shared across genome annotations including histone marks, DNase hypersensitivity, and transcription factor binding. We identify groups of TFs that suggest known shared biological mechanism, and recover correlation between DNA hypersensitivities and TF/Chromatin marks. DeepResolve is capable of visualizing complex feature contribution patterns and feature interactions that contribute to decision making in genomic deep convolutional networks. It also recovers feature sharing and class similarities which suggest interesting biological mechanisms. DeepResolve is compatible with existing visualization tools and provides complementary insights.
机译:深度学习模型的可视化工具通常专注于发现关键的输入功能,而无需考虑如何将这些低级功能组合到中间层中以做出决策。此外,许多方法都检查了网络对特定输入示例的响应,这些响应可能不足以揭示模型决策的复杂性。我们介绍了DeepResolve,这是一个用于基因组功能的深层卷积模型的分析框架,该框架可视化输入特征如何单独或组合地参与网络决策。与其他方法不同,DeepResolve不依赖于对一组预定义输入的分析。相反,它使用梯度上升来随机探索中间特征图,以:1)发现重要特征,2)可视化它们的作用和相互作用模式,以及3)分析跨任务的特征共享,从而提出共享的生物学机制。我们在训练有素的实验数据和合成数据的深度神经网络上展示了使用我们提出的方法进行决策的可视化。在发现关键序列特征方面,DeepResolve与现有的可视化工具相比具有竞争优势,并且可以识别某些负面特征和非附加特征之间的相互作用,而这些相互作用在现有工具中很难观察到。它也可以恢复相关性差的类之间的相似性,这是传统方法所无法观察到的。 DeepResolve揭示了DeepSEA学会的决策结构在基因组注释之间共享,包括组蛋白标记,DNA酶超敏反应和转录因子结合。我们确定暗示已知共享生物学机制的TF组,并恢复DNA超敏性与TF /染色质标记之间的相关性。 DeepResolve能够可视化有助于基因组深度卷积网络决策的复杂特征贡献模式和特征相互作用。它还可以恢复特征共享和类相似性,从而提示有趣的生物学机制。 DeepResolve与现有的可视化工具兼容,并提供补充的见解。

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