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Motivation
Visual inspection of microscopic images - labor-intensive, repetitive and time consuming task. Non-existence of automated technique in life science laboratories. Automation - important for medical diagnostics, planning, and treatment.
Objective
Feature extraction of known samples Master feature set creation ( Mean, Variance, Moments, Entropy) of known samples Feature set creation of test sample To classify the disease based on the minimum Euclidean distance calculation
Data
Methods
Reading pixel values Size normalisation Grey level conversion Feature extraction Minimum Euclidean distance calculation
Block Diagram
Image
Known Samples Pre Processing Feature Extraction Minimum Euclidean distance calculation Pre Processing Feature Extraction Classification
Output
Mean Calculation
Variance Calculation Moment Calculation
Read the input microscopic blood smear image. Convert the image to a Grayscale image. Resize the input image. Convert the image type to double data type. Extract Mean, Variance, 3rd order & 4th order Moment, Entropy of the image and store it in an array. Average the feature values and form a Master feature set for Normal, Elephantiasis, Trypanosomiasis, Malaria, Polycythemia and Sickle Cell Anaemia.
Variance Calculation
Moment Calculation Master feature set creation Minimum Euclidean distance calculation between the test sample and the master feature set Classification
Department of Biomedical Engineering
Read the input microscopic blood smear image that has to be tested. Convert the image to a Grayscale image and resize it. Convert the image to double data type. Extract Mean, Variance, 3rd order & 4th order Moment, Entropy of the test image and store it in an array. Calculate Minimum Euclidean distance of the feature set of the test sample with various Master feature set for Normal, Elephantiasis, Malaria, Trypanosomiasis, Polycythemia and Sickle Cell Anaemia and store it in an array. Find the minimum value of the array. Based on the minimum value, the blood smear image is classified.
Quantitative Results
Sample Mean Variance Normalized variance 0.2159 0.2095 0.2095 Moment 3rd order -0.0008 -0.0008 -0.0008 Moment 4th order 0.0002 0.0002 0.0002 Entropy Normalized entropy 0.8088 0.8163 0.7927
Normal 4
Master feature set
0.8537
0.8502
803.0929
815.5507
0.2074
0.2106
-0.0009
-0.0008
0.0002
0.0002
4.7941
4.8556
0.7924
0.8026
Elephant 1
Elephant 2 Master feature set
0.7596
0.7586 0.7591
523.3367
538.0814 530.7091
0.1351
0.1389 0.1370
-0.0012
-0.0013 -0.0013
0.0004
0.0005 0.0005
5.7054
5.7038 5.7046
0.9430
0.9427 0.9429
Cont.
Sample With normal blood smear 0.0222 0.4481 With With elephantiasis malaria blood smear blood smear 0.0128 0.0515 0.5032 0.5340 With With trypanosomiasis polycythemia blood smear blood smear 0.0348 0.4851 0.0578 0.3286 With sickle cell anaemia blood smear 0.8455 0.0365 Output
Unknown 2 Unknown 9
Unknown 10
Unknown 12 Unknown 13 Unknown 15 Unknown 16
0.0094
0.0096 0.0651 0.8243 0.1772
0.0150
0.0392 0.1813 0.8606 0.1436
0.0320
0.0192 0.0509 0.9032 0.2788
0.0164
0.00097 0.0791 0.8619 0.2265
0.0460
0.0428 0.1530 0.7380 0.0820
0.7792
0.6977 0.4556 0.2173 0.3235
normal
trypanosomasis malaria not available polycythemia
Conclusions
Advantages
Gives quantitative results for accurate diagnosis Minimal human intervention. More accurate results Synchronization of the results with interpretation from human experts. More advantageous than manual inspection Better and effective Less time consuming and less laborious Aimed at hospitals in rural areas where there is a crisis for skilled Pathologists and Lab technicians. Thus our project can be a valuable asset in the life science laboratories. In future, our project can be further extended for the detection and classification of other blood cell disorders. It can be also used for Automated Detection of cancer cells and tumors.
Conclusions
Future scope