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Weakly Supervised Learning of Single-Cell Feature Embeddings

机译:单细胞特征嵌入的弱监督学习

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We study the problem of learning representations for single cells in microscopy images to discover biological relationships between their experimental conditions. Many new applications in drug discovery and functional genomics require capturing the morphology of individual cells as comprehensively as possible. Deep convolutional neural networks (CNNs) can learn powerful visual representations, but require ground truth for training; this is rarely available in biomedical profiling experiments. While we do not know which experimental treatments produce cells that look alike, we do know that cells exposed to the same experimental treatment should generally look similar. Thus, we explore training CNNs using a weakly supervised approach that uses this information for feature learning. In addition, the training stage is regularized to control for unwanted variations using mixup or RNNs. We conduct experiments on two different datasets; the proposed approach yields single-cell embeddings that are more accurate than the widely adopted classical features, and are competitive with previously proposed transfer learning approaches.
机译:我们研究在显微镜图像中学习单个细胞的表征问题,以发现其实验条件之间的生物学关系。药物发现和功能基因组学中的许多新应用都要求尽可能全面地捕获单个细胞的形态。深度卷积神经网络(CNN)可以学习强大的视觉表示,但需要训练的基础知识。这在生物医学分析实验中很少可用。虽然我们不知道哪种实验方法会产生相似的细胞,但我们确实知道接受相同实验方法的细胞通常看起来应该相似。因此,我们使用弱监督方法探索训练CNN,该方法使用此信息进行特征学习。此外,训练阶段经过规范化,可以使用混合或RNN来控制不必要的变化。我们在两个不同的数据集上进行实验;所提出的方法所产生的单细胞嵌入比广泛采用的经典特征更准确,并且与先前提出的转移学习方法具有竞争力。

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