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C J Cogswell

Publications and source records attributed to C J Cogswell.

2 recordsLinked to original sources

Feature extraction of chromosomes from 3-D confocal microscope images.

An investigation of local energy surface detection integrated with neural network techniques for image segmentation is presented, as applied in the feature extraction of chromosomes from image datasets obtained using an experimental confocal microscope. Use of the confocal microscope enables biologists to observe dividing cells (living or preserved) within a three-dimensional (3-D) volume, that can be visualised from multiple aspects, allowing for increased structural insight. The Nomarski differential interference contrast mode used for imaging translucent specimens, such as chromosomes, produces images not suitable for volume rendering. Segmentation of the chromosomes from this data is, thus, necessary. A neural network based on competitive learning, known as Kohonen's self-organizing feature map (SOFM) was used to perform segmentation, using a collection of statistics or features defining the image. Our past investigation showed that standard features such as the localized mean and variance of pixel intensities provided reasonable extraction of objects such as mitotic chromosomes, but surface detail was only moderately resolved. In this current work, a biologically inspired feature known as local energy is investigated as an alternative image statistic based on phase congruency in the image. This, along with different combinations of other image statistics, is applied in a SOFM, producing 3-D images exhibiting vast improvement in the level of detail and clearly isolating the chromosomes from the background. Index Terms-DIC, differential interference contrast, feature extraction, feature space, image segmentation, local energy, Morlet wavelet, phase congruency, self organizing feature map, SOFM.

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Using the Hilbert transform for 3D visualization of differential interference contrast microscope images.

Differential interference contrast (DIC) is frequently used in conventional 2D biological microscopy. Our recent investigations into producing a 3D DIC microscope (in both conventional and confocal modes) have uncovered a fundamental difficulty: namely that the phase gradient images of DIC microscopy cannot be visualized using standard digital image processing and reconstruction techniques, as commonly used elsewhere in microscopy. We discuss two approaches to the problem of preparing gradient images for 3D visualization: integration and the Hilbert transform. After applying the Hilbert transform, the dataset can then be visualized in 3D using standard techniques. We find that the Hilbert transform provides a rapid qualitative pre-processing technique for 3D visualization for a wide range of biological specimens in DIC microscopy, including chromosomes, which we use in this study.

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