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Identification of masses in digital mammogram using gray level co-occurrence matrices

Digital mammogram has become the most effective technique for early breast cancer detection modality. Digital mammogram takes an electronic image of the breast and stores it directly in a computer. The aim of this study is to develop an automated system for assisting the analysis of digital mammogra...

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Autores principales: Mohd. Khuzi, A, Besar, R, Wan Zaki, WMD, Ahmad, NN
Formato: Texto
Lenguaje:English
Publicado: Department of Biomedical Imaging, Faculty of Medicine, University of Malaya, Malaysia 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3097782/
https://www.ncbi.nlm.nih.gov/pubmed/21611053
http://dx.doi.org/10.2349/biij.5.3.e17
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author Mohd. Khuzi, A
Besar, R
Wan Zaki, WMD
Ahmad, NN
author_facet Mohd. Khuzi, A
Besar, R
Wan Zaki, WMD
Ahmad, NN
author_sort Mohd. Khuzi, A
collection PubMed
description Digital mammogram has become the most effective technique for early breast cancer detection modality. Digital mammogram takes an electronic image of the breast and stores it directly in a computer. The aim of this study is to develop an automated system for assisting the analysis of digital mammograms. Computer image processing techniques will be applied to enhance images and this is followed by segmentation of the region of interest (ROI). Subsequently, the textural features will be extracted from the ROI. The texture features will be used to classify the ROIs as either masses or non-masses. In this study normal breast images and breast image with masses used as the standard input to the proposed system are taken from Mammographic Image Analysis Society (MIAS) digital mammogram database. In MIAS database, masses are grouped into either spiculated, circumscribed or ill-defined. Additional information includes location of masses centres and radius of masses. The extraction of the textural features of ROIs is done by using gray level co-occurrence matrices (GLCM) which is constructed at four different directions for each ROI. The results show that the GLCM at 0º, 45º, 90º and 135º with a block size of 8X8 give significant texture information to identify between masses and non-masses tissues. Analysis of GLCM properties i.e. contrast, energy and homogeneity resulted in receiver operating characteristics (ROC) curve area of Az = 0.84 for Otsu’s method, 0.82 for thresholding method and Az = 0.7 for K-mean clustering. ROC curve area of 0.8-0.9 is rated as good results. The authors’ proposed method contains no complicated algorithm. The detection is based on a decision tree with five criterions to be analysed. This simplicity leads to less computational time. Thus, this approach is suitable for automated real-time breast cancer diagnosis system.
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spelling pubmed-30977822011-05-24 Identification of masses in digital mammogram using gray level co-occurrence matrices Mohd. Khuzi, A Besar, R Wan Zaki, WMD Ahmad, NN Biomed Imaging Interv J Original Article Digital mammogram has become the most effective technique for early breast cancer detection modality. Digital mammogram takes an electronic image of the breast and stores it directly in a computer. The aim of this study is to develop an automated system for assisting the analysis of digital mammograms. Computer image processing techniques will be applied to enhance images and this is followed by segmentation of the region of interest (ROI). Subsequently, the textural features will be extracted from the ROI. The texture features will be used to classify the ROIs as either masses or non-masses. In this study normal breast images and breast image with masses used as the standard input to the proposed system are taken from Mammographic Image Analysis Society (MIAS) digital mammogram database. In MIAS database, masses are grouped into either spiculated, circumscribed or ill-defined. Additional information includes location of masses centres and radius of masses. The extraction of the textural features of ROIs is done by using gray level co-occurrence matrices (GLCM) which is constructed at four different directions for each ROI. The results show that the GLCM at 0º, 45º, 90º and 135º with a block size of 8X8 give significant texture information to identify between masses and non-masses tissues. Analysis of GLCM properties i.e. contrast, energy and homogeneity resulted in receiver operating characteristics (ROC) curve area of Az = 0.84 for Otsu’s method, 0.82 for thresholding method and Az = 0.7 for K-mean clustering. ROC curve area of 0.8-0.9 is rated as good results. The authors’ proposed method contains no complicated algorithm. The detection is based on a decision tree with five criterions to be analysed. This simplicity leads to less computational time. Thus, this approach is suitable for automated real-time breast cancer diagnosis system. Department of Biomedical Imaging, Faculty of Medicine, University of Malaya, Malaysia 2009-07-01 /pmc/articles/PMC3097782/ /pubmed/21611053 http://dx.doi.org/10.2349/biij.5.3.e17 Text en © 2009 Biomedical Imaging and Intervention Journal http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Mohd. Khuzi, A
Besar, R
Wan Zaki, WMD
Ahmad, NN
Identification of masses in digital mammogram using gray level co-occurrence matrices
title Identification of masses in digital mammogram using gray level co-occurrence matrices
title_full Identification of masses in digital mammogram using gray level co-occurrence matrices
title_fullStr Identification of masses in digital mammogram using gray level co-occurrence matrices
title_full_unstemmed Identification of masses in digital mammogram using gray level co-occurrence matrices
title_short Identification of masses in digital mammogram using gray level co-occurrence matrices
title_sort identification of masses in digital mammogram using gray level co-occurrence matrices
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3097782/
https://www.ncbi.nlm.nih.gov/pubmed/21611053
http://dx.doi.org/10.2349/biij.5.3.e17
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