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Flemboda artificial intelligence: hybrid fuzzy-convolutional neural network for efficient chromosome abnormality
K Kiruthika1, S Sarumathi2, M Karpagam3
1Department of Mathematics, K.S.Rangasamy College of Technology, Tiruchengode, Tamil Nadu, 637 215, India.
Molecular Genetics and Genomics : MGG
|January 20, 2026
Summary
This study introduces FLEMBODA AI, an automated system for detecting chromosomal abnormalities. The framework enhances accuracy and efficiency in clinical genetics, offering a robust solution for diagnosing genetic disorders.
Area of Science:
- Clinical Genetics
- Computational Biology
- Bioinformatics
Background:
- Accurate chromosomal abnormality detection is crucial for clinical genetics diagnosis and treatment planning.
- Existing learning-based methods struggle with capturing diverse features, limiting classification performance.
- Automated detection systems need enhanced efficiency, accuracy, and robustness.
Purpose of the Study:
- To propose FLEMBODA AI, an advanced computational framework for automated chromosome defect detection.
- To improve the efficiency, accuracy, and robustness of existing methods.
- To provide a reliable solution for clinical diagnostics and large-scale genetic analysis.
Main Methods:
- Karyotype image acquisition, augmentation, and pre-processing (normalization, G-bending enhancement).
- Chromosome segmentation using U-Net.
- Feature extraction and classification using a Hybrid Fuzzy-Convolutional Neural Network (Hybrid Fuzzy-CNN) with VGG-16 for weight assignment.
- Chromosome defect localization using Mask Region-centric CNN (Mask R-CNN).
Main Results:
- FLEMBODA AI achieved a recall of 95.3%, precision of 94.8%, and F1-score of 95.0%, outperforming baseline models.
- The U-Net segmentation model attained 93.8% accuracy.
- The framework demonstrated significant improvements in abnormality localization and classification.
Conclusions:
- FLEMBODA AI offers a reliable and effective solution for automated chromosomal abnormality detection.
- The proposed framework shows strong potential for clinical diagnostics and future genetic analysis.
- Enhanced feature capture and classification methods contribute to superior performance.
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