FreeCOS: Self-Supervised Learning from Fractals and Unlabeled Images for Curvilinear Object Segmentation

Curvilinear object segmentation is critical for many applications. However, manually annotating curvilinear objects is very time-consuming and error-prone, yielding insufficiently available annotated datasets for existing supervised methods and domain adaptation methods. This paper proposes a self-supervised curvilinear object segmentation method that learns robust and distinctive features from fractals and unlabeled images (FreeCOS). The key contributions include a novel Fractal-FDA synthesis (FFS) module and a geometric information alignment (GIA) approach. FFS generates curvilinear structures based on the parametric Fractal L-system and integrates the generated structures into unlabeled images to obtain synthetic training images via Fourier Domain Adaptation. GIA reduces the intensity differences between the synthetic and unlabeled images by comparing the intensity order of a given pixel to the values of its nearby neighbors. Such image alignment can explicitly remove the dependency on absolute intensity values and enhance the inherent geometric characteristics which are common in both synthetic and real images. In addition, GIA aligns features of synthetic and real images via the prediction space adaptation loss (PSAL) and the curvilinear mask contrastive loss (CMCL). Extensive experimental results on four public datasets, i.e., XCAD, DRIVE, STARE and CrackTree demonstrate that our method outperforms the state-of-the-art unsupervised methods, self-supervised methods and traditional methods by a large margin. The source code of this work is available at https://github.com/TY-Shi/FreeCOS.

Iterative Geometry Encoding Volume for Stereo Matching

Recurrent All-Pairs Field Transforms (RAFT) has shown great potentials in matching tasks. However, all-pairs correlations lack non-local geometry knowledge and have difficulties tackling local ambiguities in ill-posed regions. In this paper, we propose Iterative Geometry Encoding Volume (IGEV-Stereo), a new deep network architecture for stereo matching. The proposed IGEV-Stereo builds a combined geometry encoding volume that encodes geometry and context information as well as local matching details, and iteratively indexes it to update the disparity map. To speed up the convergence, we exploit GEV to regress an accurate starting point for ConvGRUs iterations. Our IGEV-Stereo ranks $1^{st}$ on KITTI 2015 and 2012 (Reflective) among all published methods and is the fastest among the top 10 methods. In addition, IGEV-Stereo has strong cross-dataset generalization as well as high inference efficiency. We also extend our IGEV to multi-view stereo (MVS), i.e. IGEV-MVS, which achieves competitive accuracy on DTU benchmark. Code is available at https://github.com/gangweiX/IGEV.

Affinity Feature Strengthening for Accurate, Complete and Robust Vessel Segmentation

Vessel segmentation is essential in many medical image applications, such as the detection of coronary stenoses, retinal vessel diseases and brain aneurysms. A high pixel-wise accuracy, complete topology structure and robustness to various contrast variations are three critical aspects of vessel segmentation. However, most existing methods only focus on achieving part of them via dedicated designs while few of them can concurrently achieve the three goals. In this paper, we present a novel affinity feature strengthening network (AFN) which adopts a contrast-insensitive approach based on multiscale affinity to jointly model topology and refine pixel-wise segmentation features. Specifically, for each pixel we derive a multiscale affinity field which captures the semantic relationships of the pixel with its neighbors on the predicted mask image. Such a multiscale affinity field can effectively represent the local topology of a vessel segment of different sizes. Meanwhile, it does not depend on image intensities and hence is robust to various illumination and contrast changes. We further learn spatial- and scale-aware adaptive weights for the corresponding affinity fields to strengthen vessel features. We evaluate our AFN on four different types of vascular datasets: X-ray angiography coronary vessel dataset (XCAD), portal vein dataset (PV), digital subtraction angiography cerebrovascular vessel dataset (DSA) and retinal vessel dataset (DRIVE). Extensive experimental results on the four datasets demonstrate that our AFN outperforms the state-of-the-art methods in terms of both higher accuracy and topological metrics, and meanwhile is more robust to various contrast changes than existing methods. Codes will be made public.