Motivated by the problem of retinal image registration, this paper introduces and analyzes a new registration algorithm called Dual-Bootstrap Iterative Closest Point (Dual-Bootstrap ICP). The approach is to start from one or more initial, low-order estimates that are only accurate in small image regions, called bootstrap regions. In each bootstrap region, the algorithm iteratively: 1) refines the transformation estimate using constraints only from within the bootstrap region; 2) expands the bootstrap region; and 3) tests to see if a higher order transformation model can be used, stopping when the region expands to cover the overlap between images. Steps 1): and 3), the bootstrap steps, are governed by the covariance matrix of the estimated transformation. Estimation refinement [Step 2)] uses a novel robust version of the ICP algorithm. In registering retinal image pairs, Dual-Bootstrap ICP is initialized by automatically matching individual vascular landmarks, and it aligns images based on detected blood vessel centerlines. The resulting quadratic transformations are accurate to less than a pixel. On tests involving approximately 6000 image pairs, it successfully registered 99.5% of the pairs containing at least one common landmark, and 100% of the pairs containing at least one common landmark and at least 35% image overlap.
Abstract-Our goal is an automated 2D-image-pair registration algorithm capable of aligning images taken of a wide variety of natural and man-made scenes as well as many medical images. The algorithm should handle low overlap, substantial orientation and scale differences, large illumination variations, and physical changes in the scene. An important component of this is the ability to automatically reject pairs that have no overlap or have too many differences to be aligned well. We propose a complete algorithm including techniques for initialization, for estimating transformation parameters, and for automatically deciding if an estimate is correct. Keypoints extracted and matched between images are used to generate initial similarity transform estimates, each accurate over a small region. These initial estimates are rank-ordered and tested individually in succession. Each estimate is refined using the Dual-Bootstrap ICP algorithm, driven by matching of multiscale features. A three-part decision criteria, combining measurements of alignment accuracy, stability in the estimate, and consistency in the constraints, determines whether the refined transformation estimate is accepted as correct. Experimental results on a data set of 22 challenging image pairs show that the algorithm effectively aligns 19 of the 22 pairs and rejects 99.8 percent of the misalignments that occur when all possible pairs are tried. The algorithm substantially out-performs algorithms based on keypoint matching alone.
This paper presents a broadly applicable algorithm and a comprehensive open-source software implementation for automated tracing of neuronal structures in 3-D microscopy images. The core 3-D neuron tracing algorithm is based on three-dimensional (3-D) open-curve active Contour (Snake). It is initiated from a set of automatically detected seed points. Its evolution is driven by a combination of deforming forces based on the Gradient Vector Flow (GVF), stretching forces based on estimation of the fiber orientations, and a set of control rules. In this tracing model, bifurcation points are detected implicitly as points where multiple snakes collide. A boundariness measure is employed to allow local radius estimation. A suite of pre-processing algorithms enable the system to accommodate diverse neuronal image datasets by reducing them to a common image format. The above algorithms form the basis for a comprehensive, scalable, and efficient software system developed for confocal or brightfield images. It provides multiple automated tracing modes. The user can optionally interact with the tracing system using multiple view visualization, and exercise full control to ensure a high quality reconstruction. We illustrate the utility of this tracing system by presenting results from a synthetic dataset, a brightfield dataset and two confocal datasets from the DIADEM challenge.
Concentric eyewall formation can be idealized as the interaction of a tropical cyclone core with nearby weaker vorticity of various spatial scales. This paper considers barotropic aspects of concentric eyewall formation from modified Rankine vortices. In this framework, the following parameters are found to be important in concentric eyewall formation: vorticity strength ratio, separation distance, companion vortex size, and core vortex skirt parameter. A vorticity skirt on the core vortex affects the filamentation dynamics in two important ways. First, the vorticity skirt lengthens the filamentation time, and therefore slows moat formation in the region just outside the radius of maximum wind. Second, at large radii, a skirted core vortex induces higher strain rates than a corresponding Rankine vortex and is thus more capable of straining out the vorticity field far from the core. Calculations suggest that concentric structures result from binary interactions when the small vortex is at least 4-6 times as strong as the larger companion vortex. An additional requirement is that the separation distance between the edges of the two vortices be less than 6-7 times the smaller vortex radius. Broad moats form when the initial companion vortex is small, the vorticity skirt outside the radius of maximum wind is small, and the strength ratio is large. In concentric cases, an outer vorticity ring develops when the initial companion vortex is large, the vorticity skirt outside the radius of maximum wind is small, and the strength ratio is not too large. In general, when the companion vortex is 3 times as strong as the core vortex and the separation distance is 4-6 times the radius of the smaller vortex, a core vortex with a vorticity skirt produces concentric structures. In contrast, a Rankine vortex produces elastic interaction in this region of parameter space. Thus, a Rankine vortex of sufficient strength favors the formation of a concentric structure closer to the core vortex, while a skirted vortex of sufficient strength favors the formation of concentric structures farther from the core vortex. This may explain satellite microwave observations that suggest a wide range of radii for concentric eyewalls.
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