Weakly Supervised Learning of Single-Cell Feature Embeddings.

Juan C Caicedo, Claire McQuin, Allen Goodman, Shantanu Singh, Anne E Carpenter
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Abstract

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.

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单细胞特征嵌入的弱监督学习
我们研究的问题是学习显微镜图像中的单细胞表征,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的许多新应用都需要尽可能全面地捕捉单个细胞的形态。深度卷积神经网络(CNN)可以学习强大的视觉表征,但需要地面实况进行训练;而这在生物医学剖析实验中很少能实现。虽然我们不知道哪些实验处理方法会产生外观相似的细胞,但我们知道暴露于相同实验处理方法下的细胞一般应该外观相似。因此,我们探索使用弱监督方法训练 CNN,利用这一信息进行特征学习。此外,我们还对训练阶段进行了正则化处理,以利用混合或 RNN 控制不必要的变化。我们在两个不同的数据集上进行了实验;所提出的方法产生的单细胞嵌入比广泛采用的经典特征更准确,与之前提出的迁移学习方法相比也更有竞争力。
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