1,154 research outputs found

    Morphology for matrix data : ordering versus PDE-based approach

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    Matrix fields are becoming increasingly important in digital imaging. In order to perform shape analysis, enhancement or segmentation of such matrix fields, appropriate image processing tools must be developed. This paper extends fundamental morphological operations to the setting of matrices, in the literature sometimes referred to as tensors despite the fact that matrices are only rank two tensors. The goal of this paper is to introduce and explore two approaches to mathematical morphology for matrix-valued data: One is based on a partial ordering, the other utilises nonlinear partial differential equations (PDEs). We start by presenting definitions for the maximum and minimum of a set of symmetric matrices since these notions are the cornerstones of the morphological operations. Our first approach is based on the Loewner ordering for symmetric matrices, and is in contrast to the unsatisfactory component-wise techniques. The notions of maximum and minimum deduced from the Loewner ordering satisfy desirable properties such as rotation invariance, preservation of positive semidefiniteness, and continuous dependence on the input data. These properties are also shared by the dilation and erosion processes governed by a novel nonlinear system of PDEs we are proposing for our second approach to morphology on matrix data. These PDEs are a suitable counterpart of the nonlinear equations known from scalar continuous-scale morphology. Both approaches incorporate information simultaneously from all matrix channels rather than treating them independently. In experiments on artificial and real medical positive semidefinite matrix-valued images we contrast the resulting notions of erosion, dilation, opening, closing, top hats, morphological derivatives, and shock filters stemming from these two alternatives. Using a ball shaped structuring element we illustrate the properties and performance of our ordering- or PDE-driven morphological operators for matrix-valued data

    Improving Fiber Alignment in HARDI by Combining Contextual PDE Flow with Constrained Spherical Deconvolution

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    We propose two strategies to improve the quality of tractography results computed from diffusion weighted magnetic resonance imaging (DW-MRI) data. Both methods are based on the same PDE framework, defined in the coupled space of positions and orientations, associated with a stochastic process describing the enhancement of elongated structures while preserving crossing structures. In the first method we use the enhancement PDE for contextual regularization of a fiber orientation distribution (FOD) that is obtained on individual voxels from high angular resolution diffusion imaging (HARDI) data via constrained spherical deconvolution (CSD). Thereby we improve the FOD as input for subsequent tractography. Secondly, we introduce the fiber to bundle coherence (FBC), a measure for quantification of fiber alignment. The FBC is computed from a tractography result using the same PDE framework and provides a criterion for removing the spurious fibers. We validate the proposed combination of CSD and enhancement on phantom data and on human data, acquired with different scanning protocols. On the phantom data we find that PDE enhancements improve both local metrics and global metrics of tractography results, compared to CSD without enhancements. On the human data we show that the enhancements allow for a better reconstruction of crossing fiber bundles and they reduce the variability of the tractography output with respect to the acquisition parameters. Finally, we show that both the enhancement of the FODs and the use of the FBC measure on the tractography improve the stability with respect to different stochastic realizations of probabilistic tractography. This is shown in a clinical application: the reconstruction of the optic radiation for epilepsy surgery planning

    Highly accurate schemes for PDE-based morphology with general structuring elements

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    The two fundamental operations in morphological image processing are dilation and erosion. These processes are defined via structuring elements. It is of practical interest to consider a variety of structuring element shapes. The realisation of dilation/erosion for convex structuring elements by use of partial differential equations (PDEs) allows for digital scalability and subpixel accuracy. However, numerical schemes suffer from blur by dissipative artifacts. In our paper we present a family of so-called flux-corrected transport (FCT) schemes that addresses this problem for arbitrary convex structuring elements. The main characteristics of the FCT-schemes are: (i) They keep edges very sharp during the morphological evolution process, and (ii) they feature a high degree of rotational invariance. We validate the FCT-scheme theoretically by proving consistency and stability. Numerical experiments with diamonds and ellipses as structuring elements show that FCT-schemes are superior to standard schemes in the field of PDE-based morphology

    Computing Interpretable Representations of Cell Morphodynamics

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    Shape changes (morphodynamics) are one of the principal ways cells interact with their environments and perform key intrinsic behaviours like division. These dynamics arise from a myriad of complex signalling pathways that often organise with emergent simplicity to carry out critical functions including predation, collaboration and migration. A powerful method for analysis can therefore be to quantify this emergent structure, bypassing the low-level complexity. Enormous image datasets are now available to mine. However, it can be difficult to uncover interpretable representations of the global organisation of these heterogeneous dynamic processes. Here, such representations were developed for interpreting morphodynamics in two key areas: mode of action (MoA) comparison for drug discovery (developed using the economically devastating Asian soybean rust crop pathogen) and 3D migration of immune system T cells through extracellular matrices (ECMs). For MoA comparison, population development over a 2D space of shapes (morphospace) was described using two models with condition-dependent parameters: a top-down model of diffusive development over Waddington-type landscapes, and a bottom-up model of tip growth. A variety of landscapes were discovered, describing phenotype transitions during growth, and possible perturbations in the tip growth machinery that cause this variation were identified. For interpreting T cell migration, a new 3D shape descriptor that incorporates key polarisation information was developed, revealing low-dimensionality of shape, and the distinct morphodynamics of run-and-stop modes that emerge at minute timescales were mapped. Periodically oscillating morphodynamics that include retrograde deformation flows were found to underlie active translocation (run mode). Overall, it was found that highly interpretable representations could be uncovered while still leveraging the enormous discovery power of deep learning algorithms. The results show that whole-cell morphodynamics can be a convenient and powerful place to search for structure, with potentially life-saving applications in medicine and biocide discovery as well as immunotherapeutics.Open Acces

    A Review of Mathematical Models for the Formation of\ud Vascular Networks

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    Mainly two mechanisms are involved in the formation of blood vasculature: vasculogenesis and angiogenesis. The former consists of the formation of a capillary-like network from either a dispersed or a monolayered population of endothelial cells, reproducible also in vitro by specific experimental assays. The latter consists of the sprouting of new vessels from an existing capillary or post-capillary venule. Similar phenomena are also involved in the formation of the lymphatic system through a process generally called lymphangiogenesis.\ud \ud A number of mathematical approaches have analysed these phenomena. This paper reviews the different modelling procedures, with a special emphasis on their ability to reproduce the biological system and to predict measured quantities which describe the overall processes. A comparison between the different methods is also made, highlighting their specific features
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