Ovidiu Ghita

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.

The process required to track cellular structures is a key task in the study of cell migration. This allows the accurate estimation of motility indicators that help in the understanding of mechanisms behind various biological processes. This paper reports a particle-based fully automatic tracking framework that is able to quantify the motility of living cells in time-lapse images. Contrary to the standard tracking methods based on predefined motion models, in this paper we reformulate the tracking mechanism as a data driven optimization process to remove its reliance on a priory motion models. The proposed method has been evaluated using 2D and 3D deconvolved epifluorescent in-vivo image sequences that describe the development of the quail embryo.