Biomedical subjects

Nilanjan Ray

Publications and source records attributed to Nilanjan Ray.

7 recordsLinked to original sources

PubMed2005

Data acceptance for automated leukocyte tracking through segmentation of spatiotemporal images.

A crucial task in inflammation research and inflammatory drug validation is leukocyte velocity data collection from microscopic video imagery. Since manual methods are bias-prone and extremely time consuming, automated tracking methods are required to compute cell velocities. However, an automated tracking method is of little practical use unless it is accompanied by a mechanism to validate the tracker output. In this paper, we propose a validation technique that accepts or rejects the output of automated tracking methods. The proposed method first generates a spatiotemporal image from the cell locations given by a tracking method; then, it segments the spatiotemporal image to detect the presence or absence of a leukocyte. For segmenting the spatiotemporal images, we employ an edge-direction sensitive nonlinear filter followed by an active contour based technique. The proposed nonlinear filter, the maximum absolute average directional derivative (MAADD), first computes the magnitude of the mean directional derivative over an oriented line segment and then chooses the maximum of all such values within a range of orientations of the line segment. The proposed active contour segmentation is obtained via growing contours controlled by a two-dimensional force field, which is constructed by imposing a Dirichlet boundary condition on the gradient vector flow (GVF) field equations. The performance of the proposed validation method is reported here for the outputs of three different tracking techniques: the method was successful in 97% of the trials using manual tracking, in 94% using correlation tracking and in 93% using active contour tracking.

Algorithms↗

PubMed2005

Inclusion filters: a class of self-dual connected operators.

In this paper, we define a connected operator that either fills or retains the holes of the connected sets depending on application-specific criteria that are increasing in the set theoretic sense. We refer to this class of connected operators as inclusion filters, which are shown to be increasing, idempotent, and self dual (gray-level inversion invariance). We demonstrate self duality for 8-adjacency on a discrete Cartesian grid. Inclusion filters are defined first for binary-valued images, and then the definition is extended to grayscale imagery. It is also shown that inclusion filters are levelings, a larger class of connected operators. Several important applications of inclusion filters are demonstrated-automatic segmentation of the lung cavities from magnetic resonance imagery, user interactive shape delineation in content-based image retrieval, registration of intravital microscopic video sequences, and detection and tracking of cells from these sequences. The numerical performance measures on 100-cell tracking experiments show that the use of inclusion filter improves the total number of frames successfully tracked by five times and provides a threefold reduction in the overall position error.

Algorithms↗

PubMed2005

Intravital leukocyte detection using the gradient inverse coefficient of variation.

The problem of identifying and counting rolling leukocytes within intravital microscopy is of both theoretical and practical interest. Currently, methods exist for tracking rolling leukocytes in vivo, but these methods rely on manual detection of the cells. In this paper we propose a technique for accurately detecting rolling leukocytes based on Bayesian classification. The classification depends on a feature score, the gradient inverse coefficient of variation (GICOV), which serves to discriminate rolling leukocytes from a cluttered environment. The leukocyte detection process consists of three sequential steps: the first step utilizes an ellipse matching algorithm to coarsely identify the leukocytes by finding the ellipses with a locally maximal GICOV. In the second step, starting from each of the ellipses found in the first step, a B-spline snake is evolved to refine the leukocytes boundaries by maximizing the associated GICOV score. The third and final step retains only the extracted contours that have a GICOV score above the analytically determined threshold. Experimental results using 327 rolling leukocytes were compared to those of human experts and currently used methods. The proposed GICOV method achieves 78.6% leukocyte detection accuracy with 13.1% false alarm rate.

Algorithms↗

PubMed2004

Level set analysis for leukocyte detection and tracking.

We propose a cell detection and tracking solution using image-level sets computed via threshold decomposition. In contrast to existing methods where manual initialization is required to track individual cells, the proposed approach can automatically identify and track multiple cells by exploiting the shape and intensity characteristics of the cells. The capture of the cell boundary is considered as an evolution of a closed curve that maximizes image gradient along the curve enclosing a homogeneous region. An energy functional dependent upon the gradient magnitude along the cell boundary, the region homogeneity within the cell boundary and the spatial overlap of the detected cells is minimized using a variational approach. For tracking between frames, this energy functional is modified considering the spatial and shape consistency of a cell as it moves in the video sequence. The integrated energy functional complements shape-based segmentation with a spatial consistency based tracking technique. We demonstrate that an acceptable, expedient solution of the energy functional is possible through a search of the image-level lines: boundaries of connected components within the level sets obtained by threshold decomposition. The level set analysis can also capture multiple cells in a single frame rather than iteratively computing a single active contour for each individual cell. Results of cell detection using the energy functional approach and the level set approach are presented along with the associated processing time. Results of successful tracking of rolling leukocytes from a number of digital video sequences are reported and compared with the results from a correlation tracking scheme.

Algorithms↗

PubMed2004

Motion gradient vector flow: an external force for tracking rolling leukocytes with shape and size constrained active contours.

Recording rolling leukocyte velocities from intravital microscopic video imagery is a critical task in inflammation research and drug validation. Since manual tracking is excessively time consuming, an automated method is desired. This paper illustrates an active contour based automated tracking method, where we propose a novel external force to guide the active contour that takes the hemodynamic flow direction into account. The construction of the proposed force field, referred to as motion gradient vector flow (MGVF), is accomplished by minimizing an energy functional involving the motion direction, and the image gradient magnitude. The tracking experiments demonstrate that MGVF can be used to track both slow- and fast-rolling leukocytes, thus extending the capture range of previously designed cell tracking techniques.

Algorithms↗

PubMed2003

Merging parametric active contours within homogeneous image regions for MRI-based lung segmentation.

Inhaled hyperpolarized helium-3 (3He) gas is a new magnetic resonance (MR) contrast agent that is being used to study lung functionality. To evaluate the total lung ventilation from the hyperpolarized 3He MR images, it is necessary to segment the lung cavities. This is difficult to accomplish using only the hyperpolarized 3He MR images, so traditional proton (1H) MR images are frequently obtained concurrent with the hyperpolarized 3He MR examination. Segmentation of the lung cavities from traditional proton (1H) MRI is a necessary first step in the analysis of hyperpolarized 3He MR images. In this paper, we develop an active contour model that provides a smooth boundary and accurately captures the high curvature features of the lung cavities from the 1H MR images. This segmentation method is the first parametric active contour model that facilitates straightforward merging of multiple contours. The proposed method of merging computes an external force field that is based on the solution of partial differential equations with boundary condition defined by the initial positions of the evolving contours. A theoretical connection with fluid flow in porous media and the proposed force field is established. Then by using the properties of fluid flow we prove that the proposed method indeed achieves merging and the contours stop at the object boundary as well. Experimental results involving merging in synthetic images are provided. The segmentation technique has been employed in lung 1H MR imaging for segmenting the total lung air space. This technology plays a key role in computing the functional air space from MR images that use hyperpolarized 3He gas as a contrast agent.

Administration, Inhalation↗

PubMed2002

Tracking leukocytes in vivo with shape and size constrained active contours.

Inflammatory disease is initiated by leukocytes (white blood cells) rolling along the inner surface lining of small blood vessels called postcapillary venules. Studying the number and velocity of rolling leukocytes is essential to understanding and successfully treating inflammatory diseases. Potential inhibitors of leukocyte recruitment can be screened by leukocyte rolling assays and successful inhibitors validated by intravital microscopy. In this paper, we present an active contour or snake-based technique to automatically track the movement of the leukocytes. The novelty of the proposed method lies in the energy functional that constrains the shape and size of the active contour. This paper introduces a significant enhancement over existing gradient-based snakes in the form of a modified gradient vector flow. Using the gradient vector flow, we can track leukocytes rolling at high speeds that are not amenable to tracking with the existing edge-based techniques. We also propose a new energy-based implicit sampling method of the points on the active contour that replaces the computationally expensive explicit method. To enhance the performance of this shape and size constrained snake model, we have coupled it with Kalman filter so that during coasting (when the leukocytes are completely occluded or obscured), the tracker may infer the location of the center of the leukocyte. Finally, we have compared the performance of the proposed snake tracker with that of the correlation and centroid-based trackers. The proposed snake tracker results in superior performance measures, such as reduced error in locating the leukocyte under tracking and improvements in the percentage of frames successfully tracked. For screening and drug validation, the tracker shows promise as an automated data collection tool.

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