Systems Biology of Development, University of Konstanz, Konstanz, Germany.
Friedrich Miescher Laboratory of the Max Planck Society, Tübingen, Germany.
Nat Methods. 2023 Jun;20(6):815-823. doi: 10.1038/s41592-023-01873-4. Epub 2023 May 8.
Evolutionarily conserved signaling pathways are essential for early embryogenesis, and reducing or abolishing their activity leads to characteristic developmental defects. Classification of phenotypic defects can identify the underlying signaling mechanisms, but this requires expert knowledge and the classification schemes have not been standardized. Here we use a machine learning approach for automated phenotyping to train a deep convolutional neural network, EmbryoNet, to accurately identify zebrafish signaling mutants in an unbiased manner. Combined with a model of time-dependent developmental trajectories, this approach identifies and classifies with high precision phenotypic defects caused by loss of function of the seven major signaling pathways relevant for vertebrate development. Our classification algorithms have wide applications in developmental biology and robustly identify signaling defects in evolutionarily distant species. Furthermore, using automated phenotyping in high-throughput drug screens, we show that EmbryoNet can resolve the mechanism of action of pharmaceutical substances. As part of this work, we freely provide more than 2 million images that were used to train and test EmbryoNet.
进化保守的信号通路对于早期胚胎发生至关重要,减少或消除它们的活性会导致特征性的发育缺陷。表型缺陷的分类可以确定潜在的信号机制,但这需要专业知识,并且分类方案尚未标准化。在这里,我们使用机器学习方法进行自动表型分析,训练深度卷积神经网络 EmbryoNet 以无偏方式准确识别斑马鱼信号突变体。结合时间依赖性发育轨迹模型,该方法可以识别和分类高精确度的表型缺陷,这些缺陷是由与脊椎动物发育相关的七个主要信号通路的功能丧失引起的。我们的分类算法在发育生物学中有广泛的应用,并能在进化上相距甚远的物种中稳健地识别信号缺陷。此外,我们使用高通量药物筛选中的自动表型分析,表明 EmbryoNet 可以解析药物物质的作用机制。作为这项工作的一部分,我们免费提供了超过 200 万张用于训练和测试 EmbryoNet 的图像。