探索显微镜图像表示的自监督学习偏差。

Biological imaging Pub Date : 2024-11-14 eCollection Date: 2024-01-01 DOI:10.1017/S2633903X2400014X
Ihab Bendidi, Adrien Bardes, Ethan Cohen, Alexis Lamiable, Guillaume Bollot, Auguste Genovesio
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引用次数: 0

摘要

计算机视觉中的自监督表示学习(SSRL)在很大程度上依赖于简单的图像变换,如随机旋转、作物或照明,以学习有意义和不变的特征。尽管承认转型选择的重要性,但文献中缺乏对转型选择影响的全面探索。我们的研究深入到这种关系,特别关注显微镜成像与微妙的细胞表型差异。我们揭示了转换设计作为一种有害或有益的监督形式,影响特征聚类和表示相关性。重要的是,这些效果根据监督数据集中的类标签而变化。在显微镜图像中,变换设计显著影响表征,引入难以察觉但强烈的偏差。我们证明了基于期望特征不变性的策略转换选择,即使在有限的训练样本下也能极大地提高分类性能和表示质量。
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Exploring self-supervised learning biases for microscopy image representation.

Self-supervised representation learning (SSRL) in computer vision relies heavily on simple image transformations such as random rotation, crops, or illumination to learn meaningful and invariant features. Despite acknowledged importance, there is a lack of comprehensive exploration of the impact of transformation choice in the literature. Our study delves into this relationship, specifically focusing on microscopy imaging with subtle cell phenotype differences. We reveal that transformation design acts as a form of either unwanted or beneficial supervision, impacting feature clustering and representation relevance. Importantly, these effects vary based on class labels in a supervised dataset. In microscopy images, transformation design significantly influences the representation, introducing imperceptible yet strong biases. We demonstrate that strategic transformation selection, based on desired feature invariance, drastically improves classification performance and representation quality, even with limited training samples.

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Deep-learning-based image compression for microscopy images: An empirical study. The quest for early detection of retinal disease: 3D CycleGAN-based translation of optical coherence tomography into confocal microscopy. Bridging the gap: Integrating cutting-edge techniques into biological imaging with deepImageJ. Deep-blur: Blind identification and deblurring with convolutional neural networks. Exploring self-supervised learning biases for microscopy image representation.
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