Abstract
Scientists wishing to communicate the essential characteristics of a pattern (such as an immunofluorescence distribution) currently must make a subjective choice of one or two images to publish. We therefore developed methods for objectively choosing a typical image from a set, with emphasis on images from cell biology. The methods involve calculation of numerical features to describe each image, calculation of similarity between images as a distance in feature space, and ranking of images by distance from the center of the feature distribution. Two types of features were explored, image texture measures and Zernike polynomial moments, and various distance measures were utilized. Criteria for evaluating methods for assigning typicality were proposed and applied to sets of images containing more than one pattern. The results indicate the importance of using distance measures that are insensitive to the presence of outliers. For collections of images of the distributions of a lysosomal protein, a Golgi protein, and nuclear DNA, the images chosen as most typical were in good agreement with the conventional understanding of organelle morphologies. The methods described here have been implemented in a web server (http://murphylab.web.cmu.edu/services/TyplC).
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Selected References
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- Boland M. V., Markey M. K., Murphy R. F. Automated recognition of patterns characteristic of subcellular structures in fluorescence microscopy images. Cytometry. 1998 Nov 1;33(3):366–375. [PubMed] [Google Scholar]
- Farkas D. L., Baxter G., DeBiasio R. L., Gough A., Nederlof M. A., Pane D., Pane J., Patek D. R., Ryan K. W., Taylor D. L. Multimode light microscopy and the dynamics of molecules, cells, and tissues. Annu Rev Physiol. 1993;55:785–817. doi: 10.1146/annurev.ph.55.030193.004033. [DOI] [PubMed] [Google Scholar]
- Fleming M. G. Design of a high resolution image cytometer with open software architecture. Anal Cell Pathol. 1996 Jan;10(1):1–11. [PubMed] [Google Scholar]