Debojyoti Biswas

Debojyoti Biswas, Jelena Tešić

State-of-the-art object detection methods applied to satellite and drone imagery largely fail to identify small and dense objects. One reason is the high variability of content in the overhead imagery due to the terrestrial region captured and the high variability of acquisition conditions. Another reason is that the number and size of objects in aerial imagery are very different than in the consumer data. In this work, we propose a small object detection pipeline that improves the feature extraction process by spatial pyramid pooling, cross-stage partial networks, heatmap-based region proposal network, and object localization and identification through a novel image difficulty score that adapts the overall focal loss measure based on the image difficulty. Next, we propose novel contrastive learning with progressive domain adaptation to produce domain-invariant features across aerial datasets using local and global components. We show we can alleviate the degradation of object identification in previously unseen datasets. We create a first-ever domain adaptation benchmark using contrastive learning for the object detection task in highly imbalanced satellite datasets with significant domain gaps and dominant small objects. The proposed method results in a 7.4% increase in mAP performance measure over the best state-of-art.

Aditya Shankar Pal, Debojyoti Biswas, Joy Mahapatra et al.

White blood cells (WBCs) play a crucial role in safeguarding the human body against pathogens and foreign substances. Leveraging the abundance of WBC imaging data and the power of deep learning algorithms, automated WBC analysis has the potential for remarkable accuracy. However, the capability of deep learning models to explain their WBC classification remains largely unexplored. In this study, we introduce HemaX, an explainable deep neural network-based model that produces pathologist-like explanations using five attributes: granularity, cytoplasm color, nucleus shape, size relative to red blood cells, and nucleus to cytoplasm ratio (N:C), along with cell classification, localization, and segmentation. HemaX is trained and evaluated on a novel dataset, LeukoX, comprising 467 blood smear images encompassing ten (10) WBC types. The proposed model achieves impressive results, with an average classification accuracy of 81.08% and a Jaccard index of 89.16% for cell localization. Additionally, HemaX performs well in generating the five explanations with a normalized mean square error of 0.0317 for N:C ratio and over 80% accuracy for the other four attributes. Comprehensive experiments comparing against multiple state-of-the-art models demonstrate that HemaX's classification accuracy remains unaffected by its ability to provide explanations. Moreover, empirical analyses and validation by expert hematologists confirm the faithfulness of explanations predicted by our proposed model.

Iftekhar Ahmed, Shakib Absar, Aftar Ahmad Sami et al.

Precise segmentation of retinal arteries and veins carries the diagnosis of systemic cardiovascular conditions. However, standard convolutional architectures often yield topologically disjointed segmentations, characterized by gaps and discontinuities that render reliable graph-based clinical analysis impossible despite high pixel-level accuracy. To address this, we introduce a topology-aware framework engineered to maintain vascular connectivity. Our architecture fuses a Topological Feature Fusion Module (TFFM) that maps local feature representations into a latent graph space, deploying Graph Attention Networks to capture global structural dependencies often missed by fixed receptive fields. Furthermore, we drive the learning process with a hybrid objective function, coupling Tversky loss for class imbalance with soft clDice loss to explicitly penalize topological disconnects. Evaluation on the Fundus-AVSeg dataset reveals state-of-the-art performance, achieving a combined Dice score of 90.97% and a 95% Hausdorff Distance of 3.50 pixels. Notably, our method decreases vessel fragmentation by approximately 38% relative to baselines, yielding topologically coherent vascular trees viable for automated biomarker quantification. We open-source our code at https://tffm-module.github.io/.