U-Net:用于生物医学图像分割的卷积网络

U-Net: Convolutional Networks for Biomedical Image Segmentation

奥拉夫·罗内贝格尔 Olaf Ronneberger · University of Freiburg · 2015-05-18 · arXiv:1505.04597 ↗ · 被引 97700

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摘要 · Abstract

人们普遍认为,深度网络的成功训练需要数千个带注释的训练样本。在本文中,我们提出了一种网络和训练策略,该策略依赖于数据增强的强力使用,以更有效地利用可用的注释样本。该架构由一个用于捕获上下文的收缩路径和一个能够实现精确定位的对称扩展路径组成。我们表明,这样的网络可以从非常少的图像中进行端到端训练,并且在电子显微镜堆栈中神经元结构分割的 ISBI 挑战中优于先前的最佳方法(滑动窗口卷积网络)。使用在透射光显微镜图像(相差和 DIC)上训练的相同网络,我们在 2015 年 ISBI 细胞追踪挑战赛中大幅领先。此外,该网络速度很快。在最新的 GPU 上,分割 512x512 图像只需不到一秒。完整实现(基于 Caffe)和训练好的网络可在 http://lmb.informatik.uni-freiburg.de/people/ronneber/u-net 获取。

There is large consent that successful training of deep networks requires many thousand annotated training samples. In this paper, we present a network and training strategy that relies on the strong use of data augmentation to use the available annotated samples more efficiently. The architecture consists of a contracting path to capture context and a symmetric expanding path that enables precise localization. We show that such a network can be trained end-to-end from very few images and outperforms the prior best method (a sliding-window convolutional network) on the ISBI challenge for segmentation of neuronal structures in electron microscopic stacks. Using the same network trained on transmitted light microscopy images (phase contrast and DIC) we won the ISBI cell tracking challenge 2015 in these categories by a large margin. Moreover, the network is fast. Segmentation of a 512x512 image takes less than a second on a recent GPU. The full implementation (based on Caffe) and the trained networks are available at http://lmb.informatik.uni-freiburg.de/people/ronneber/u-net .

核心贡献 · Key contributions

局限 · Limitations

论文章节 · Sections(共 8)

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