Paper
9 March 2011 Toward automated quantification of biological microstructures using unbiased stereology
Om Pavithra Bonam, Daniel Elozory, Kurt Kramer, Dmitry Goldgof, Lawrence O. Hall, Osvaldo Mangual, Peter R. Mouton
Author Affiliations +
Abstract
Quantitative analysis of biological microstructures using unbiased stereology plays a large and growing role in bioscience research. Our aim is to add a fully automatic, high-throughput mode to a commercially available, computerized stereology device (Stereologer). The current method for estimation of first- and second order parameters of biological microstructures, requires a trained user to manually select objects of interest (cells, fibers etc.,) while stepping through the depth of a stained tissue section in fixed intervals. The proposed approach uses a combination of color and gray-level processing. Color processing is used to identify the objects of interest, by training on the images to obtain the threshold range for objects of interest. In gray-level processing, a region-growing approach was used to assign a unique identity to the objects of interest and enumerate them. This automatic approach achieved an overall object detection rate of 93.27%. Thus, these results support the view that automatic color and gray-level processing combined with unbiased sampling and assumption and model-free geometric probes can provide accurate and efficient quantification of biological objects.
© (2011) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Om Pavithra Bonam, Daniel Elozory, Kurt Kramer, Dmitry Goldgof, Lawrence O. Hall, Osvaldo Mangual, and Peter R. Mouton "Toward automated quantification of biological microstructures using unbiased stereology", Proc. SPIE 7963, Medical Imaging 2011: Computer-Aided Diagnosis, 79633G (9 March 2011); https://doi.org/10.1117/12.878710
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KEYWORDS
Image processing

Image segmentation

Tissues

Biological research

Computing systems

Microscopy

Binary data

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