{"id":19685,"date":"2018-03-25T09:44:07","date_gmt":"2018-03-25T09:44:07","guid":{"rendered":"http:\/\/biomedpharmajournal.org\/?p=19685"},"modified":"2020-04-23T06:03:25","modified_gmt":"2020-04-23T06:03:25","slug":"textures-and-intensity-histogram-based-retinal-image-classification-system-using-hybrid-colour-structure-descriptor","status":"publish","type":"post","link":"https:\/\/biomedpharmajournal.org\/staging\/vol11no1\/textures-and-intensity-histogram-based-retinal-image-classification-system-using-hybrid-colour-structure-descriptor\/","title":{"rendered":"Textures and Intensity Histogram Based Retinal Image Classification System Using Hybrid Colour Structure Descriptor"},"content":{"rendered":"<p><strong>Introduction<\/strong><\/p>\n<p>Medical images are used for investigation, education and research and hence its security is of vital importance. Therefore many authentication techniques have been proposed to protect the medical images. Medical images can be split into ROI and RONI portions. ROI is a key area in the medical image as it is used by doctors for investigation and treatment. Medical images are dissimilar in nature. Therefore ROI selection itself is a problem because ROI of different modalities disparate. Even ROIs of two head CT are unlike. There is also a possibility of having multiple ROIs in an image. Therefore automatic feature detection methods could be useful in identifying ROI and RONI. Automated image segmentation shall also be to discriminate ROI and RONI. These tools have the advantage of minimising the task of manual inspection. Another advantage of automated tools is that there is no need to send the ROI vertices to the receiver as it is required by the receiver for verification.<sup>1-2<\/sup><\/p>\n<p>Glaucoma is a degenerative and progressive optic neuropathy which ranks as the second most disabling and blinding disease worldwide. Early diagnosis is the key to prevent progressive and irreversible damage to retinal nerve fibers\u2019 functionality. Funduscopic sign of the retinalnerve fiber layer (RNFL) defect provides an early objective evidence of structural changes inglaucoma which is caused due to the loss of retinal ganglion cell axons.<sup>3<\/sup> Before the visualfield defect begins, the ganglion cells have already sustained a loss of about 50%.<sup>4<\/sup> Current imaging techniques like optical coherence tomography (OCT), GDx offering RNFLD assessment are expensive and require careful interpretation by experts. Moreover, these imaging techniquesare not feasible solution for mass screening and routine checkup of glaucoma in peripheralsettings. In this regard, computer-aided lesion detection using retinal image provides apractical solution for efficient glaucoma risk assessment.<sup>5-6<\/sup><\/p>\n<p>Several studies have been reported in the literature that utilize data-driven approaches to sub-divide a given ROI into several functional subROIs. One approach is clustering based on features, for example the Pearson&#8217;s pair-wise correlation between each voxel&#8217;s time course within the ROI with that of other brain regions, and then a clustering algorithm is applied to divide the voxels into several sub-groups.<sup>7-10<\/sup> However, most clustering methods require rigorous preprocessing and denoising steps to obtain spatially continuous results since they are very sensitive to outliers. Another approach, based on graph theory, is where each voxel within the ROI is rep-resented by a node in a graph. This graph is then divided into subROIs using modularity detection<sup>11<\/sup>\u00a0 or a normalized cut approach.<sup>12<\/sup> Furthermore, the robustness of the method highly depends on its optimization parameters and tuning the parameters is a challenging task. Therefore there is still a need for a complete framework for functional subROI parcellation that can incorporate both the inter-ROI and intra-ROI connectivity patterns while imposing spatial continuity for subROIs.<sup>13<\/sup> The rest of the paper is organized as follows: Our proposed feature extraction technique is given in section 2 and feature classification is given in section 3. The detailed experimental results and discussions are given in section 4, while the conclusion is summarized in section 4.<\/p>\n<p><strong>Multi Model Feature Extraction Process<\/strong><\/p>\n<p>Diabetic retinopathy is an ocular manifestation of diabetes, and diabetics are at a risk of loss of eyesight due to diabetic retinopathy. In our proposed feature extraction system consists of colour, structure and shape.The proposed method feature process consists of the following stages<\/p>\n<p><strong>Computing Feature Vector <\/strong>\u00a0<strong>H(V<sub>1<\/sub>)<\/strong><\/p>\n<p>In this work, original image is divided into 4, 18, and 24 grids. The grids are normally square in shape. Gridding results in smaller grids, so that the analysis can be performed easily, then the Feature vector H(V<sub>1<\/sub>) is calculated for each intensity values 1 to 255of the original image.<\/p>\n<p><strong>Feature Vector \u00a0H(V<sub>2<\/sub>) using Orientation <\/strong><\/p>\n<p>Spatial Gray Level Dependence Matrix technique (SGLDM) is\u00a0 utilized in each ROI to extract second ordermeasurable texture\u00a0 features\u00a0 for\u00a0 the\u00a0 analysis.<sup>14<\/sup> This\u00a0 system is\u00a0 in\u00a0 light of the\u00a0 estimation of\u00a0 second order jointconditional\u00a0 likelihood\u00a0 density\u00a0 functions<\/p>\n<p><img decoding=\"async\" class=\"alignnone size-full wp-image-19688\" src=\"https:\/\/biomedpharmajournal.org\/wp-content\/uploads\/2018\/03\/Vol11No1_Tex_Jay_f1.jpg\" alt=\"F1\" width=\"277\" height=\"40\" \/><\/p>\n<p>Where angle (\u03b8) is varies from 0 to 180 degrees. Each P(i, j | d,\u03b8 ) is the likelihood grid of two pixels which are placed with a inter test distance d and direction \u03b8having a gray level i to j. The calculated value for these likelihood density function is given by<\/p>\n<p><img decoding=\"async\" class=\"alignnone size-full wp-image-19689\" src=\"https:\/\/biomedpharmajournal.org\/wp-content\/uploads\/2018\/03\/Vol11No1_Tex_Jay_f2.jpg\" alt=\"F2\" width=\"360\" height=\"43\" srcset=\"https:\/\/biomedpharmajournal.org\/staging\/wp-content\/uploads\/2018\/03\/Vol11No1_Tex_Jay_f2-300x36.jpg 300w, https:\/\/biomedpharmajournal.org\/staging\/wp-content\/uploads\/2018\/03\/Vol11No1_Tex_Jay_f2.jpg 360w\" sizes=\"(max-width: 360px) 100vw, 360px\" \/><\/p>\n<p>where Ng is maximum grey level. In this technique, four gray level co-occurrence matrixes for four different directions are acquired for a given distance and the following five statistical texture features are computed for each gray level co-occurrence matrix. Finally, the features such as correlation ,homogeneity, contrast, energy and entropy are extracted and stored in the feature vector H(V<sub>2<\/sub>).<\/p>\n<p><strong>Feature Vector <\/strong><strong>H(V<sub>3<\/sub>)<\/strong> <strong>using <\/strong><strong>TCM<\/strong><\/p>\n<p>In Texton co-occurrence matrix (TCM), they divided the image into non-overlapping 2 \u00d7 2 sub blocks and then they collected the relationship between the pixel gray values in a 2 \u00d7 2 sub block for texton image generation. After calculation of texton image, co-occurrence matrix operation is performed on the texton image to form the final feature vector generation. Figure 1 illustrates the texton shapes which are considered for the texton image generation.<\/p>\n<table style=\"width: 70%;\" border=\"1\" cellpadding=\"5\">\n<tbody>\n<tr>\n<td><img decoding=\"async\" class=\"alignnone size-thumbnail wp-image-19693\" src=\"https:\/\/biomedpharmajournal.org\/wp-content\/uploads\/2018\/03\/Vol11No1_Tex_Jay_fig1-150x150.jpg\" alt=\"Figure 1: Different shape of the texton for feature extraction\" width=\"150\" height=\"150\" srcset=\"https:\/\/biomedpharmajournal.org\/staging\/wp-content\/uploads\/2018\/03\/Vol11No1_Tex_Jay_fig1-150x150.jpg 150w, https:\/\/biomedpharmajournal.org\/staging\/wp-content\/uploads\/2018\/03\/Vol11No1_Tex_Jay_fig1-256x256.jpg 256w, https:\/\/biomedpharmajournal.org\/staging\/wp-content\/uploads\/2018\/03\/Vol11No1_Tex_Jay_fig1.jpg 542w\" sizes=\"(max-width: 150px) 100vw, 150px\" \/><\/td>\n<td><strong>Figure 1: Different shape of the texton for feature extraction<\/strong><\/p>\n<p>&nbsp;<\/p>\n<p><a href=\"http:\/\/biomedpharmajournal.org\/wp-content\/uploads\/2018\/03\/Vol11No1_Tex_Jay_fig1.jpg\" target=\"_blank\">Click here to View figure<\/a><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>&nbsp;<\/p>\n<p>Then, the block count value is calculated for each intensity value (1-255) on this image. The resultant feature vector\u00a0 H(V<sub>3<\/sub>) is obtained from the micro structure image<\/p>\n<p><strong>Feature Vector H(V<sub>4<\/sub>) using RGB Plane<\/strong><\/p>\n<p>Feature vector H(V<sub>4<\/sub>) is calculated using Red, Green and Blue plane separately, Here, the relationship of RGB plane of retinal image calculation process is given in the following figure (2). In this technique, the edge detection algorithm is applied in Green plane then the corresponding relationship of Red and Blue plane pixel values are in a 3&#215;3 matrix using various binary pattern , finally the feature vector H(V<sub>4<\/sub>) is calculated using histogram.<\/p>\n<table style=\"width: 70%;\" border=\"1\" cellpadding=\"5\">\n<tbody>\n<tr>\n<td>\u00a0<img decoding=\"async\" class=\"alignnone size-thumbnail wp-image-19694\" src=\"https:\/\/biomedpharmajournal.org\/wp-content\/uploads\/2018\/03\/Vol11No1_Tex_Jay_fig2-150x150.jpg\" alt=\"Figure 2: Feature vector F(V4) calculation process\" width=\"150\" height=\"150\" srcset=\"https:\/\/biomedpharmajournal.org\/staging\/wp-content\/uploads\/2018\/03\/Vol11No1_Tex_Jay_fig2-150x150.jpg 150w, https:\/\/biomedpharmajournal.org\/staging\/wp-content\/uploads\/2018\/03\/Vol11No1_Tex_Jay_fig2-256x256.jpg 256w, https:\/\/biomedpharmajournal.org\/staging\/wp-content\/uploads\/2018\/03\/Vol11No1_Tex_Jay_fig2.jpg 651w\" sizes=\"(max-width: 150px) 100vw, 150px\" \/><\/td>\n<td><strong>Figure 2: Feature vector F(V4) calculation process<\/strong><\/p>\n<p>&nbsp;<\/p>\n<p><a href=\"http:\/\/biomedpharmajournal.org\/wp-content\/uploads\/2018\/03\/Vol11No1_Tex_Jay_fig2.jpg\" target=\"_blank\">Click here to View figure<\/a><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>&nbsp;<\/p>\n<p><strong>Concatenated of Four Feature Vectors<\/strong><\/p>\n<p>Finally the feature vector H(V1),H(V2), H(V3) and H(V4) are concatenated and generate a feature vector H(V)is used for\u00a0 feature \u00a0classification. It is defined as follows\u00a0<em>H(V) = H(V<sub>1<\/sub>) + H(V<sub>2<\/sub>) + H(V<sub>3<\/sub>) + H(V<sub>4<\/sub>)<\/em><\/p>\n<p><strong>Feature Classification<\/strong><\/p>\n<p>In our feature classification system, various \u00a0kernels functions are combined and to develop a novel retinal image classification system \u00a0using SVM. It\u00a0 is\u00a0 a\u00a0 statistical\u00a0 classi\ufb01cation algorithm developed using structural risk\u00a0 minimization methods.<sup>15-16<\/sup> It classifies the data into two separate classes that is normal classes and abnormal classes. In SVM, the kernel functions are used to maximize the margin between different classes. The margin is 1\/||w||. Maximizing the margin 1\/||w|| is equivalent to minimizing ||w||<sup>2<\/sup>, whose solution is found after resolving the following quadratic optimization problem:<\/p>\n<p><img decoding=\"async\" class=\"alignnone size-full wp-image-19690\" src=\"https:\/\/biomedpharmajournal.org\/wp-content\/uploads\/2018\/03\/Vol11No1_Tex_Jay_f3.jpg\" alt=\"F3\" width=\"516\" height=\"90\" srcset=\"https:\/\/biomedpharmajournal.org\/staging\/wp-content\/uploads\/2018\/03\/Vol11No1_Tex_Jay_f3-300x52.jpg 300w, https:\/\/biomedpharmajournal.org\/staging\/wp-content\/uploads\/2018\/03\/Vol11No1_Tex_Jay_f3.jpg 516w\" sizes=\"(max-width: 516px) 100vw, 516px\" \/><\/p>\n<p>By using the duality theory of optimization is defined as follows<\/p>\n<p><img decoding=\"async\" class=\"alignnone size-full wp-image-19691\" src=\"https:\/\/biomedpharmajournal.org\/wp-content\/uploads\/2018\/03\/Vol11No1_Tex_Jay_f4.jpg\" alt=\"F3\" width=\"283\" height=\"89\" \/><\/p>\n<p>There are several kernel functions, and the generally used kernel functions are given as follows:<\/p>\n<p>Linear kernel <em>k (x,x<sub>i<\/sub>) = (x<sup>T<\/sup> x<sub>i<\/sub>)<\/em><\/p>\n<p>Polynomial kernel\u00a0<em>k (x,x<sub>i<\/sub>) = (\u03b3 (x<sup>T<\/sup> x<sub>i<\/sub>) +r)<sup>d <\/sup>,\u03b3&gt;0<\/em><\/p>\n<p>RBF kernel\u00a0<em>k (x,x<sub>i<\/sub>) = exp(-||\u03b3 x &#8211; x<sub>i<\/sub> ||<sup>2<\/sup>) ,\u03b3&gt;0<\/em><\/p>\n<p>Sigmoid kernel\u00a0<em>k (x,x<sub>i<\/sub>) =tanh (\u03b3 (x<sup>T<\/sup>, x<sub>i<\/sub>) +r)<\/em><\/p>\n<p>Where y,d,r are kernel parameter for each kernel function<\/p>\n<p><strong>Experimental Results and Comparative Analysis <\/strong><\/p>\n<p>The experimental image data set contains 100 retinal images ( 80 images for abnormal and the remaining 20 images for normal)\u00a0 that are collected from Government medical college hospital, Tirunelveli, Tamilnadu, India. The normal and abnormal image is shown in Fig 2.<\/p>\n<table style=\"width: 70%;\" border=\"1\" cellpadding=\"5\">\n<tbody>\n<tr>\n<td>\u00a0<img decoding=\"async\" class=\"alignnone size-thumbnail wp-image-19695\" src=\"https:\/\/biomedpharmajournal.org\/wp-content\/uploads\/2018\/03\/Vol11No1_Tex_Jay_fig2a-150x150.jpg\" alt=\"Figure 2a: Normal and abnormal retinal images\" width=\"150\" height=\"150\" srcset=\"https:\/\/biomedpharmajournal.org\/staging\/wp-content\/uploads\/2018\/03\/Vol11No1_Tex_Jay_fig2a-150x150.jpg 150w, https:\/\/biomedpharmajournal.org\/staging\/wp-content\/uploads\/2018\/03\/Vol11No1_Tex_Jay_fig2a-256x256.jpg 256w, https:\/\/biomedpharmajournal.org\/staging\/wp-content\/uploads\/2018\/03\/Vol11No1_Tex_Jay_fig2a.jpg 586w\" sizes=\"(max-width: 150px) 100vw, 150px\" \/><\/td>\n<td><strong>Figure 2a: Normal and abnormal retinal images<\/strong><\/p>\n<p>&nbsp;<\/p>\n<p><a href=\"http:\/\/biomedpharmajournal.org\/wp-content\/uploads\/2018\/03\/Vol11No1_Tex_Jay_fig2a.jpg\" target=\"_blank\">Click here to View figure<\/a><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>&nbsp;<\/p>\n<p>The classification performance of our proposed system is evaluated using the following metrics such as sensitivity,specificity and accuracy.<sup>17<\/sup><\/p>\n<p><em>Sensitivity = TP\/(TP+FN)<\/em><\/p>\n<p><em>Specificity = TN\/(TN+FP)<\/em><\/p>\n<p><em>Accuracy = (TN+TP)\/(TN + TP+ FN+FP)<\/em><\/p>\n<p><em>Error rate = 1 &#8211; Accuracy<\/em><\/p>\n<p>The investigational results of CSID with Hybrid SVM and other neural network based classifier are shown in Table 1 and the results are visualized in Figure 3.<\/p>\n<p><strong>Table 1: Experimental results of the proposed and exiting system<\/strong><\/p>\n<table style=\"width: 95%;\" border=\"1\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr>\n<td colspan=\"2\" rowspan=\"2\" width=\"162\">\n<p style=\"text-align: center;\"><strong>Evaluation metrics<\/strong><\/p>\n<\/td>\n<td style=\"text-align: center;\" rowspan=\"2\" width=\"81\"><strong>CSID +\u00a0<\/strong><strong>SVM<\/strong><\/td>\n<td style=\"text-align: center;\" rowspan=\"2\" width=\"76\"><strong>CSID+ RBF<\/strong><\/td>\n<td style=\"text-align: center;\" rowspan=\"2\" width=\"76\"><strong>CSID<\/strong><strong> + FFNN<\/strong><\/td>\n<td style=\"text-align: center;\" colspan=\"2\" width=\"161\"><strong>Our Proposed Approach<\/strong><\/td>\n<\/tr>\n<tr>\n<td style=\"text-align: center;\" width=\"85\"><strong>k1+k2<\/strong><\/td>\n<td style=\"text-align: center;\" width=\"76\"><strong>k1 k2<\/strong><\/td>\n<\/tr>\n<tr>\n<td style=\"text-align: center;\" rowspan=\"7\" width=\"55\">Input MRI image data set<\/td>\n<td style=\"text-align: center;\" width=\"107\">True Positive(TP)<\/td>\n<td style=\"text-align: center;\" width=\"81\">37<\/td>\n<td style=\"text-align: center;\" width=\"76\">35<\/td>\n<td style=\"text-align: center;\" width=\"76\">30<\/td>\n<td style=\"text-align: center;\" width=\"85\">38<\/td>\n<td style=\"text-align: center;\" width=\"76\">38<\/td>\n<\/tr>\n<tr>\n<td style=\"text-align: center;\" width=\"107\">True Negative(TN)<\/td>\n<td style=\"text-align: center;\" width=\"81\">8<\/td>\n<td style=\"text-align: center;\" width=\"76\">7<\/td>\n<td style=\"text-align: center;\" width=\"76\">6<\/td>\n<td style=\"text-align: center;\" width=\"85\">9<\/td>\n<td style=\"text-align: center;\" width=\"76\">9<\/td>\n<\/tr>\n<tr>\n<td style=\"text-align: center;\" width=\"107\">False Positive(FP)<\/td>\n<td style=\"text-align: center;\" width=\"81\">2<\/td>\n<td style=\"text-align: center;\" width=\"76\">3<\/td>\n<td style=\"text-align: center;\" width=\"76\">4<\/td>\n<td style=\"text-align: center;\" width=\"85\">1<\/td>\n<td style=\"text-align: center;\" width=\"76\">1<\/td>\n<\/tr>\n<tr>\n<td style=\"text-align: center;\" width=\"107\">False Negative(FN)<\/td>\n<td style=\"text-align: center;\" width=\"81\">3<\/td>\n<td style=\"text-align: center;\" width=\"76\">5<\/td>\n<td style=\"text-align: center;\" width=\"76\">10<\/td>\n<td style=\"text-align: center;\" width=\"85\">2<\/td>\n<td style=\"text-align: center;\" width=\"76\">2<\/td>\n<\/tr>\n<tr>\n<td style=\"text-align: center;\" width=\"107\">Sensitivity<\/td>\n<td style=\"text-align: center;\" width=\"81\">0.925<\/td>\n<td style=\"text-align: center;\" width=\"76\">0.875<\/td>\n<td style=\"text-align: center;\" width=\"76\">0.75<\/td>\n<td style=\"text-align: center;\" width=\"85\">0.95<\/td>\n<td style=\"text-align: center;\" width=\"76\">0.95<\/td>\n<\/tr>\n<tr>\n<td style=\"text-align: center;\" width=\"107\">Specificity<\/td>\n<td style=\"text-align: center;\" width=\"81\">0.8<\/td>\n<td style=\"text-align: center;\" width=\"76\">0.7<\/td>\n<td style=\"text-align: center;\" width=\"76\">0.6<\/td>\n<td style=\"text-align: center;\" width=\"85\">0.9<\/td>\n<td style=\"text-align: center;\" width=\"76\">0.9<\/td>\n<\/tr>\n<tr>\n<td style=\"text-align: center;\" width=\"107\">Accuracy<\/td>\n<td style=\"text-align: center;\" width=\"81\">0.9<\/td>\n<td style=\"text-align: center;\" width=\"76\">0.84<\/td>\n<td style=\"text-align: center;\" width=\"76\">0.72<\/td>\n<td style=\"text-align: center;\" width=\"85\">0.94<\/td>\n<td style=\"text-align: center;\" width=\"76\">0.94<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>&nbsp;<\/p>\n<table style=\"width: 70%;\" border=\"1\" cellpadding=\"5\">\n<tbody>\n<tr>\n<td>\u00a0<img decoding=\"async\" class=\"alignnone size-thumbnail wp-image-19696\" src=\"https:\/\/biomedpharmajournal.org\/wp-content\/uploads\/2018\/03\/Vol11No1_Tex_Jay_fig3-150x150.jpg\" alt=\"Figure 3: Comparison results of CSID with SVM, RBF , FFNN and HKSVM\" width=\"150\" height=\"150\" srcset=\"https:\/\/biomedpharmajournal.org\/staging\/wp-content\/uploads\/2018\/03\/Vol11No1_Tex_Jay_fig3-150x150.jpg 150w, https:\/\/biomedpharmajournal.org\/staging\/wp-content\/uploads\/2018\/03\/Vol11No1_Tex_Jay_fig3-256x256.jpg 256w, https:\/\/biomedpharmajournal.org\/staging\/wp-content\/uploads\/2018\/03\/Vol11No1_Tex_Jay_fig3.jpg 769w\" sizes=\"(max-width: 150px) 100vw, 150px\" \/><\/td>\n<td><strong>Figure 3: Comparison results of CSID with SVM, RBF , FFNN and HKSVM<\/strong><\/p>\n<p>&nbsp;<\/p>\n<p><a href=\"http:\/\/biomedpharmajournal.org\/wp-content\/uploads\/2018\/03\/Vol11No1_Tex_Jay_fig3.jpg\" target=\"_blank\">Click here to View figure<\/a><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>&nbsp;<\/p>\n<p><strong>Conclusion<\/strong><\/p>\n<p>Manual segmentation results look better because it involves human intelligence but the disadvantage is that the results may differ from one person to another person and takes long time. A novel\u00a0 fully automatic , multi class image classification approach using Color image hybrid structure descriptor and pair of RBF kernel based SVM has been developed. In this research work ,Pair of RBF kernel functions are combined\u00a0 for multi class retinal image\u00a0 classification. The overall classification accuracy of \u00a0HCSID with\u00a0 HKSVM is 94%, HCSID with\u00a0 SVM is 90 % \u00a0HCSID with\u00a0 RBF is 84% and HCSID with\u00a0 FFNN is 84%..<\/p>\n<p><strong>Reference<\/strong><\/p>\n<ol>\n<li>Juuti-Uusitalo K., Delporte C., Gr\u00e9goire F., Perret J., Huhtala H., Savolainen V., et al. Aquaporin expressionand function in human pluripotent stem cell-derived retinal pigmented epithelial cells. <em>Invest Ophthalmol.Vis Sci.<\/em> 2013;54:3510\u20133519.<br \/>\n<a href=\"https:\/\/doi.org\/10.1167\/iovs.13-11800\" target=\"_blank\">CrossRef<\/a><\/li>\n<li>Schwartz S. D., Hubschman J. P., Heilwell G., Franco-Cardenas V., Pan C. K., Ostrick R. M., et al. 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