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A supervised framework is presented for the automatic registration and segmentation of white matter (WM) tractographies extracted from brain DT-MRI. The framework relies on the direct registration between the fibers, without requiring any intensity-based registration as preprocessing. An affine transform is recovered together with a set of segmented fibers. A recently introduced probabilistic boosting tree classifier is used in a segmentation refinement step to improve the precision of the target tract segmentation. The proposed method compares favorably with a state-of-the-art intensity-based algorithm for affine registration of DTI tractographies. Segmentation results for 12 major WM tracts are demonstrated. Quantitative results are also provided for the segmentation of a particularly difficult case, the optic radiation tract. An average precision of 80% and recall of 55% were obtained for the optimal configuration of the presented method. [ABSTRACT FROM AUTHOR]

In this paper, we present a robust approach to the registration of white matter tractographies extracted from diffusion tensor-magnetic resonance imaging scans. The fibers are projected into a high dimensional feature space based on the sequence of their 3-D coordinates. Adaptive mean-shift clustering is applied to extract a compact set of representative fiber-modes (FM). Each FM is assigned to a multivanate Gaussian distribution according to its population thereby leading to a Gaussian mixture model (GMM) representation for the entire set of fibers. The registration between two fiber sets is treated as the alignment of two GMMs and is performed by maximizing their correlation ratio. A nine-parameters affine transform is recovered and eventually refined to a twelve-parameters affine transform using an innovative mean-shift based registration refinement scheme presented in this paper. The validation of the algorithm on synthetic intrasubject data demonstrates its robustness to interrupted and deviating fiber artifacts as well as outliers. Using real intrasubject data, a comparison is conducted to other intensity based and fiber-based registration algorithms, demonstrating competitive results. An option for tracking-in-time, on specific white matter fiber tracts, is also demonstrated on the real data. [ABSTRACT FROM AUTHOR]

Histopathological analysis is crucial for the diagnosis of a large number of cancer types. A lot of progress has been made in the development of molecular based assays, but many of the cases still require the careful analysis of the stained tissue under a bright-field microscope and its analysis. This procedure is costly and time-consuming. We present a novel method for classification of cancer cells in lymph node images. It is based on the measurement of the spectral image of hematoxylin and eosin stained sample under the microscope and the analysis of the acquired data using state of the art machine learning techniques. The method is based on the analysis of the spectral information of the cells as well as their morphological properties. A large number of descriptors is extracted for each cell location, which are used to train a supervised classifier which discriminates between normal and cancer cells. We show that a reliable analysis can be made with detection rate (recall) of 81%-100% for the cancer class.

Extravasation during intravenous (IV) infusion is a common secondary effect with potentially serious clinical consequences. The correct positioning of the needle in the vein may be difficult to confirm when no blood return is observed. In this paper, a novel method is proposed for the detection of extravasation during infusion therapy. A small volume of a sodium bicarbonate solution is administrated IV and, following its consecutive dissociation, an excess of carbon dioxide (CO2) is rapidly exhaled by the lungs. The analysis of the exhaled CO2 signal by a pattern recognition algorithm enables the robust detection of the CO2 excess release, thereby confirming the absence of extravasation. Initial results are presented for the application of the method on a group of 89 oncology patients.