Deep Learning Architectures� for Automated Malaria Diagnostics
Dominik Polzer
Problem definition
Dominik
Polzer
Solution approach
Model ID | Size (MB) | Epochs | F1 Score | Technical Status |
Model 0 | 4.04 | 10 | 98% | Baseline model (No augmentation) |
Model 3 | 4.04 | 7 | 97% | Good Generalization (augmentation) |
Model 4 | 58.20 | 3 | ~95% | Bouncy Validation (High Learning rate) |
Model 2 | 18.95 | 9 | ~91% | Slight overfitting Issue |
Model 5 | 58.29 | 5 | ~90% | Augmentation + PT |
Model 1 | 18.92 | 5 | FAIL | pre-processing fail |
All models compared in the process of finding the best classification model.
Proposed model solution
97%
F1-SCORE PEAK
7 Epochs / 4.04MB
Model 3:
Model 3 training process
Proposed business solution
Dominik Polzer
Appendix
More info on the hyperparameters chosen in the code -
shown in the next few slides …
Predictions - Confusion matrix
Model 3
Model predictions
We can observe some of the Model3 classification results.
False positives
Model 3 CNN Architecture
Pre-processing - Augmentation hyper-params
Model 3 training dataset preprocessing utilized these selected augmentation hyperparameters.
Comparison vs VGG16 architecture
Top 4 observed models
Model training /fitting process.
Notice the sharp val_accuracy jumps in model 4 and 5.
This was likely caused by non optimal HIGH learning rate(0.001) hyper-parameter.
Resource references:
VGG 16 Architecture
WHO - Malaria report 2025
Dominik Polzer