Proceedings of the Twenty-Second National Radio Science Conference, 2005. NRSC 2005. 2005
DOI: 10.1109/nrsc.2005.194026
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Segmentation and classification of multispectral chromosome biages

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Cited by 3 publications
(3 citation statements)
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“…Color compensation techniques are explained in [5].In this author conclude that by analyzing the intensity combinations of each pixel, all chromosome pixels in an image are classified. Use of Discrete Wavelet Transform (DWT) and Bayes rule for M-FISH image segmentation and classification is presented in [6].Classification of multicolor fluorescence in situ hybridization images using Gaussian mixture models is discussed in [7]. Use of support vector machines (SVM) for segmentation and classification of M-FISH image was described in [8].…”
Section: Literature Surveymentioning
confidence: 99%
“…Color compensation techniques are explained in [5].In this author conclude that by analyzing the intensity combinations of each pixel, all chromosome pixels in an image are classified. Use of Discrete Wavelet Transform (DWT) and Bayes rule for M-FISH image segmentation and classification is presented in [6].Classification of multicolor fluorescence in situ hybridization images using Gaussian mixture models is discussed in [7]. Use of support vector machines (SVM) for segmentation and classification of M-FISH image was described in [8].…”
Section: Literature Surveymentioning
confidence: 99%
“…Mohammed et al [8] presented an automated method for segmentation and classification of multispectral chromosome images. They used adaptive thresholding and valley searching for background cancellation.…”
Section: Literature Surveymentioning
confidence: 99%
“…There are two main types of chromosome abnormalities, namely 1) structural abnormality and 2) numerical abnormality (insertion or deletion of chromosome copies) [9]- [10]. The former type needs visible chromosome banding with resolution above 500, while the latter type needs to count the total number of chromosomes and banding at high resolution may not be needed, e.g., checking chromosome 21 trisomy.…”
Section: Introductionmentioning
confidence: 99%