Abstract:The Industrial Conference on Data Mining ICDM-Leipzig was the sixth event in a series of annual events which started in 2000. We are pleased to note that the topic data mining with special emphasis on real world applications has been adopted from so many researchers all over the world into their research work. We received 156 papers from 19 different countries. The main topics are data mining in medicine and marketing, web mining, mining of images and signals, theoretical aspects of data mining, and aspects of… Show more
“…This approach is fragile because small islands of noisy pixels can cause over-segmentations. Tscherepanow et al [25] presented an active contour approach with a snakes formulation wherein overlapping cells are segmented as dictated by a 2D elliptical model. Jones et al [4] presented a novel method that first defines a metric in the image plane for calculating distances from seed regions.…”
Section: Related Workmentioning
confidence: 99%
“…All of the approaches discussed above rely on using information derived either from cellular shape models [25] or internuclear gradients [4] or neck shape cues [24]. It is interesting to note that no single approach elegantly incorporates all the cues into the segmentation process.…”
Section: Related Workmentioning
confidence: 99%
“…Identifying each nucleus separately in a biologically consistent fashion is non-trivial. While some histological stains provide viable clues in the form of sharp color-space gradients at the boundaries [4], others exhibit a narrow neck at the site of overlap between two nuclei [25]. Please refer, for example, to Figure 1(b) wherein a pair of nuclei are shown with color gradients and a narrow neck indicated by the white arrows.…”
Abstract-Developments in optical microscopy imaging have generated large high-resolution datasets that have spurred medical researchers to conduct investigations into mechanisms of disease, including cancer, at cellular and sub-cellular levels. The work reported here demonstrates that a suitable methodology can be conceived which isolates modality-dependent effects from the larger segmentation task and that 3D reconstructions can be cognizant of shapes as evident in the available 2D planar images. In the current realization, a method based on active geodesic contours is first deployed to counter the ambiguity that exists in separating overlapping cells on the image plane. Later, another segmentation effort based on a variant of Voronoi tessellations improves the delineation of the cell boundaries using a Bayesian formulation. In the next stage, the cells are interpolated across the third dimension thereby mitigating the poor structural correlation that exists in that dimension. We deploy our methods on three separate datasets obtained from light, confocal and phase-contrast bright field microscopy and validate the results appropriately.
“…This approach is fragile because small islands of noisy pixels can cause over-segmentations. Tscherepanow et al [25] presented an active contour approach with a snakes formulation wherein overlapping cells are segmented as dictated by a 2D elliptical model. Jones et al [4] presented a novel method that first defines a metric in the image plane for calculating distances from seed regions.…”
Section: Related Workmentioning
confidence: 99%
“…All of the approaches discussed above rely on using information derived either from cellular shape models [25] or internuclear gradients [4] or neck shape cues [24]. It is interesting to note that no single approach elegantly incorporates all the cues into the segmentation process.…”
Section: Related Workmentioning
confidence: 99%
“…Identifying each nucleus separately in a biologically consistent fashion is non-trivial. While some histological stains provide viable clues in the form of sharp color-space gradients at the boundaries [4], others exhibit a narrow neck at the site of overlap between two nuclei [25]. Please refer, for example, to Figure 1(b) wherein a pair of nuclei are shown with color gradients and a narrow neck indicated by the white arrows.…”
Abstract-Developments in optical microscopy imaging have generated large high-resolution datasets that have spurred medical researchers to conduct investigations into mechanisms of disease, including cancer, at cellular and sub-cellular levels. The work reported here demonstrates that a suitable methodology can be conceived which isolates modality-dependent effects from the larger segmentation task and that 3D reconstructions can be cognizant of shapes as evident in the available 2D planar images. In the current realization, a method based on active geodesic contours is first deployed to counter the ambiguity that exists in separating overlapping cells on the image plane. Later, another segmentation effort based on a variant of Voronoi tessellations improves the delineation of the cell boundaries using a Bayesian formulation. In the next stage, the cells are interpolated across the third dimension thereby mitigating the poor structural correlation that exists in that dimension. We deploy our methods on three separate datasets obtained from light, confocal and phase-contrast bright field microscopy and validate the results appropriately.
“…Unstained cell recognition in bright-field images is a challenging problem [20], [21], [36], [38], [42]. Cells exhibit a great diversity in shape and size.…”
Abstract-We present a novel machine learning-based system for unstained cell detection in bright-field microscope images. The system is fully automatic since it requires no manual parameter tuning. It is also highly invariant with respect to illumination conditions and to the size and orientation of cells. Images from two adherent cell lines and one suspension cell line were used in the evaluation for a total number of more than 3500 cells. Besides real images, simulated images were also used in the evaluation. The detection error was between approximately zero and 15.5% which is a significantly superior performance compared to baseline approaches.
“…Several previous object recognition techniques have attempted to detect and count sf9 cells in bright-field images using active contour models. 4,5 Active contour models do not work satisfactorily in the presence of strong texture and pixel intensity variation, which is a characteristic of the amplitude contrast images. The broader literature review shows that not much work has been done on automatic analysis of bright-field cell data.…”
This article presents a methodology for acquisition and analysis of bright-field amplitude contrast image data in highthroughput screening (HTS) for the measurement of cell density, cell viability, and classification of individual cells into phenotypic classes. We present a robust image analysis pipeline, where the original data are subjected to image standardization, image enhancement, and segmentation by region growing. This work develops new imaging and analysis techniques for cell analysis in HTS and successfully addresses a particular need for direct measurement of cell density and other features without using dyes.
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