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Identification of Diabetic Retinopathy Using The Retinal Images

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IDENTIFICATION OF DIABETIC

RETINOPATHY USING THE RETINAL


IMAGES

Department of ECE

-by
M.Ayisha sithika
M.Basima banu
K.Gayathri
Batch number :111
Under the supervision of
Miss
L.C.MEENA(Asst.PROFESSOR) , 1
AIM
 To identify diabetic retinopathy using the retinal images in an
efficient manner.
 Exudates is one of the features used to identify the
diabetic retinopathy .

OBJECTIVE

 Exudates ,a very important and mostly occurring feature


of retinopathy is identified using k-means and naives bayes
classifier.

2
INTRODUCTION-EYE
INTRODUCTION-DIABETIC
RETINOPAHTY
DIABETIC RETINOPATHY
• DR is an eye disease which has been caused due to high blood
sugar level.

TYPES OF DR

1) Non-proliferative diabetic retinopathy


2) Diabetic maculopathy
3) Proliferative diabetic retinopathy
Normal Defective
EXUDATES

• Primary sign of diabetic retinopathy


• It is lipids and proteins leaks from damaged
blood vessels.

FUNDUS IMAGE OF EYE

• FUNDUS OF EYE: The back portion of the interior of


the eyeball, visible through the pupil by use of the
ophthalmoscope.

• FUNDUS IMAGE: Fundus photography is performed by a


fundus camera, which basically consists of a specialized
low power microscope with an attached camera.
LITREATURE SURVEY
1.Akara Sopharak , Bunyarit Uyyanonvara and Sarah Barman[6],
“Automatic Exudate Detection from Non-dilated Diabetic
Retinopathy-Retinal Images Using Fuzzy C-means Clustering”.

ADVANTAGES:
 The low contrast retinal image- intensity increased
and a
number of edge pixels were extracted.

DISADVANTAGES:
 More time consuming.

7
2.T. Walter, J. Klein, P. Massin, and A. Erginary[2],“A
contribution of image processing to the diagnosis of
diabetic retinopathy thy,detection of exudates in colour
fundus images of the human retina".

ADVANTAGES:
 Time consumption reduced as it uses mathematical
is morphology
techniques .
DISADVANTAGES:
 The paper ignored some types of errors on the border
of the segmented exudates in their reported performances.
 Time consumption is reduced but not to great extent. 8
NOVELTY USED

• In our project we are using k-means clustering algorithm with


naive bayes classifier.

• Fuzzy c-means algorithm, as consumes time, so k-means


is used to reduce time.

• Naive bayes,a type of classifier is used to increase


the accuracy and sensitivity of the detection.

9
WORK ACCOMPLISHED

BLOCK DIAGRAM:

INPUT
PRE- FEATURE
RETINAL SEGMENTATION
PROCESSING EXTRACTION
IMAGE

EXUDATES

CLASSIFICATION

NON-
EXUDATES
STEP 1:PRE-PROCESSING

RGB to HIS
image

Median
filtering

CLAHE

HSI to RGB
image
STEP 2:IMAGE SEGMENTATION

RGB to a*b alone


l*a*b colour using k-means five clusters
space clustering

Colour
optic disc is labels every
segmented
localized pixel
images
STEP 3:FEATURE EXTRACTION

• On the basis of colour and texture


orientation, features are extracted using
GLCM.

STEP 4: CLASSIFICATION

• The final step is classification of given input as


exudates (or) non-exudates by naive bayes
classifier.
PRE-PROCESSED OUTPUT

Input retinal image

HSI Components

H component S Component I Component


Filtered I component CLAHE image Pre-processed image
SEGMENTATION OUTPUT
LAB colour space images

a. L channel b. A channel c. B channel


Image Labeled By Cluster Index
CLUSTER FORMATION

cluster1 cluster2 cluster3

cluster4 cluster5

Cluster Output
EXECUTION OF FINAL OUTPUT
CONCLUSION
• The selected features clustered by k-means clustering and
classified into exudates and non –exudates using naive
bayes classifier.
• Using this approach, the exudates are detected with 98%
success rate.

FUTURE WORK

• Detection of Micro-aneurysm and also maculopathy be


predicted and performance can be compared.
REFERENCES
1 Wynne Hsu, P M D S Pallawala, Mong Li Lee, KahGuan Au Eong(2001),”The Role
of Domain Knowledge in the Detection of Retinal Hard Exudates”, IEEE
Conference on Computer Vision and Pattern Recognition (CVPR), Kauai Marriott,
Hawaii, vol.12,pp. 533-548.

2 T. Walter, J.Klein, P.Massin and A.Erginary(2002), “A Contribution of image


processing to the diagnosis of Diabetic Retinopathy detection of exudates in color
fundus images of the human retina”, IEEE Trans. On Med. images, vol. 21, no.
10,
pp. 1236-1243.

3 Pizer. S.M(2003),“The Medical Image Display and analysis group at the university
of North Carolina:Reminiscences and philosophy ”, IEEE Trans On Medical
Imaging, vol. 22, no. 1, pp. 2-10.

4 Fleming. AD, Philips. S, Goatman. KA, Williams. GJ, Olson.JA, sharp.


PF(2007),“Automated detection of exudates for Diabetic Retinopathy Screening”,
Journal of Phys. Med. Bio., vol. 52, no. 24, pp. 7385-7396.

5 Alireza Osareh, Bita Shadgar, and Richard Markham(2009), “A Computational-


Intelligence-Based Approach for Detection of Exudates in Diabetic Retinopathy
Images”,IEEE Transactions on Information Technology in Biomedicine,vol. 13,
no. 4,pp.535-545.International Diabetic Federation (IDF), 2009a, Latest diabetes
• [6] Akara Sopharak, Bunyarit Uyyanonvara, Sarah Barman(2009), “Automatic Exudate
Detection from Non-dilated Diabetic Retinopathy retinal images using Fuzzy Cleans
Clustering” Journal of Sensors, vol.9, No. 3, pp 2148- 2161.

• [7] Saiprasad Ravishankar, Arpit Jain, Anurag Mittal(2009),“Automated feature extraction for
early detection of Diabetic Retinopathy in fundus images”,IEEE Conference on Computer
vision and pattern Recognition, pp. 210-217.

• [8] Doaa Youssef, Nahed Solouma, Amr El-dib, Mai Mabrouk(2010),“New Feature-Based
Detection of Blood Vessels and Exudates in Color Fundus Images” IEEE conference on Image
Processing Theory, Tools and Applications, vol.16,pp.294-299

• [9] Guoliang Fang, Nan Yang, Huchuan Lu and Kaisong Li(2010),“Automatic


Segmentation of Hard Exudates in fundus images based on Boosted Soft Segmentation”,
International Conference on Intelligent Control and Information Processing, vol.13,pp. 633-
638.

• [10] Plissiti.M.E., Nikar.C, Charchanti.A(2011),“Automated detection of cell nuclei in


pap smear images using morphological reconstruction and clustering” IEEE Trans. On
Insformation Technology in Biomedicine, vol. 2, pp. 233-241.
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