This paper evaluates the performance of state of the art colour invariants for the purposes of local image feature detection. We adapt the Harris-Laplace detector for colour invariance and test it under general image distortions. A second investigation examines the correlation between the colour invariants where the number of correctly detected unique points are analysed. This paper aims to answer if colour invariants should be used for feature detection purposes, and if they could be jointly used by feature fusion techniques to augment the performance of intensity-based detectors.

In this paper, we investigate the segmentation of closed contours in subcellular data using a framework that primarily combines the pairwise affinity grouping principles with a graph partitioning contour searching approach. One salient problem that precluded the application of these methods to large scale segmentation problems is the onerous computational complexity required to generate comprehensive representations that include all pairwise relationships between all pixels in the input data. To compensate for this problem, a practical solution is to reduce the complexity of the input data by applying an over-segmentation technique prior to the application of the computationally demanding strands of the segmentation process. This approach opens the opportunity to build specific shape and intensity models that can be successfully employed to extract the salient structures in the input image which are further processed to identify the cycles in an undirected graph. The proposed framework has been applied to the segmentation of mitochondria membranes in electron microscopy data which are characterized by low contrast and low signal-to-noise ratio. The algorithm has been quantitatively evaluated using two datasets where the segmentation results have been compared with the corresponding manual annotations. The performance of the proposed algorithm has been measured using standard metrics, such as precision and recall, and the experimental results indicate a high level of segmentation accuracy.

Histogram transformation defines a class of image processing operations that are widely applied in the implementation of data normalization algorithms. In this paper, we present a new variational approach for image enhancement that is constructed to alleviate the intensity saturation effects that are introduced by standard contrast enhancement (CE) methods based on histogram equalization. In this paper, we initially apply total variation (TV) minimization with a L(1) fidelity term to decompose the input image with respect to cartoon and texture components. Contrary to previous papers that rely solely on the information encompassed in the distribution of the intensity information, in this paper, the texture information is also employed to emphasize the contribution of the local textural features in the CE process. This is achieved by implementing a nonlinear histogram warping CE strategy that is able to maximize the information content in the transformed image. Our experimental study addresses the CE of a wide variety of image data and comparative evaluations are provided to illustrate that our method produces better results than conventional CE strategies.

The aim of this paper is to detail the development of a novel tracking framework that is able to extract the cell motility indicators and to determine the cellular division (mitosis) events in large time-lapse phase-contrast image sequences. To address the challenges induced by nonstructured (random) motion, cellular agglomeration, and cellular mitosis, the process of automatic (unsupervised) cell tracking is carried out in a sequential manner, where the interframe cell association is achieved by assessing the variation in the local cellular structures in consecutive frames of the image sequence. In our study, a strong emphasis has been placed on the robust use of the topological information in the cellular tracking process and in the development of targeted pattern recognition techniques that were designed to redress the problems caused by segmentation errors, and to precisely identify mitosis using a backward (reversed) tracking strategy. The proposed algorithm has been evaluated on dense phase-contrast cellular data and the experimental results indicate that the proposed algorithm is able to accurately track epithelial and endothelial cells in time-lapse image sequences that are characterized by low contrast and high level of noise. Our algorithm achieved 86.10% overall tracking accuracy and 90.12% mitosis detection accuracy.

A common approach to model-based segmentation is to assume a top-down modelling strategy. However, this is not feasible for complex 3D +time structures, such as the cardiac left ventricle, due to increased training requirements, aligning difficulties and local minima in resulting models. As our main contribution, we present an alternate bottom-up modelling approach. By combining the variation captured in multiple dimensionally-targeted models at segmentation-time we create a scalable segmentation framework that does not suffer from the "curse of dimensionality." Our second contribution involves a flexible contour coupling technique that allows our segmentation method to adapt to unseen contour configurations outside the training set. This is used to identify the endo- and epicardium contours of the left ventricle by coupling them at segmentation-time, instead of at model-time. We apply our approach to 33 3D +time cardiac MRI datasets and perform comprehensive evaluation against several state-of-the-art works. Quantitative evaluation illustrates that our method requires significantly less training than state-of-the-art model-based methods, while maintaining or improving segmentation accuracy.

With the proliferation of modern microscopy imaging technologies the amount of data that has to be analysed by biologists is constantly increasing and as a result the development of automatic approaches that are able to track cellular structures in time-lapse images has become an important field of research. The aim of this paper is to detail the development of a novel tracking framework that is designed to extract the cell motility indicators in phase-contrast image sequences. To address issues that are caused by non-structured (random) motion and cellular agglomeration, cell tracking is formulated as a sequential process where the inter-frame cell association is achieved by assessing the variation in the local structures contained in consecutive frames of the image sequence. We have evaluated the proposed algorithm on dense phase contrast cellular data and the reported results indicate that the developed algorithm is able to accurately track Madin-Darby Canine Kidney (MDCK) Epithelial Cells in image data that is characterised by low contrast and high level of noise.

The advent of new hyperspectral imaging modalities made possible the implementation of flexible machine vision systems that can be designed to solve a variety of industrial tasks such as automatic material sorting. However the design of robust machine vision systems is far from a trivial task as several issues including mechanical design, development of an appropriate illumination set-up, optimal interfacing between the sensing and optical equipment with the computer vision component have to be properly addressed in order to accommodate all challenges that are encountered in a typical industrial environment. In this paper we present a novel methodology to automate the recycling process of non-ferrous metal Waste from Electric and Electronic Equipment (WEEE) where a particular emphasis is placed on the design choices that were made in the development of the proposed waste sorting system. The developed machine vision system has been subjected to a thorough robustness evaluation and the reported experimental results indicate that the proposed solution can be used to replace the manual procedure that is currently used in WEEE recycling plants.

Hyperspectral data allows the construction of more elaborate models to sample the properties of the nonferrous materials than the standard RGB color representation. In this paper, the nonferrous waste materials are studied as they cannot be sorted by classical procedures due to their color, weight and shape similarities. The experimental results presented in this paper reveal that factors such as the various levels of oxidization of the waste materials and the slight differences in their chemical composition preclude the use of the spectral features in a simplistic manner for robust material classification. To address these problems, the proposed FUSSER (fuzzy spectral and spatial classifier) algorithm detailed in this paper merges the spectral and spatial features to obtain a combined feature vector that is able to better sample the properties of the nonferrous materials than the single pixel spectral features when applied to the construction of multivariate Gaussian distributions. This approach allows the implementation of statistical region merging techniques in order to increase the performance of the classification process. To achieve an efficient implementation, the dimensionality of the hyperspectral data is reduced by constructing bio-inspired spectral fuzzy sets that minimize the amount of redundant information contained in adjacent hyperspectral bands. The experimental results indicate that the proposed algorithm increased the overall classification rate from 44% using RGB data up to 98% when the spectral-spatial features are used for nonferrous material classification.

Modern medical imaging modalities provide large amounts of information in both the spatial and temporal domains and the incorporation of this information in a coherent algorithmic framework is a significant challenge. In this paper, we present a novel and intuitive approach to combine 3-D spatial and temporal (3-D + time) magnetic resonance imaging (MRI) data in an integrated segmentation algorithm to extract the myocardium of the left ventricle. A novel level-set segmentation process is developed that simultaneously delineates and tracks the boundaries of the left ventricle muscle. By encoding prior knowledge about cardiac temporal evolution in a parametric framework, an expectation-maximization algorithm optimally tracks the myocardial deformation over the cardiac cycle. The expectation step deforms the level-set function while the maximization step updates the prior temporal model parameters to perform the segmentation in a nonrigid sense.