The rapid adoption of electric vehicles (EVs) has intensified the demand for intelligent, scalable, and interoperable charging infrastructure. Traditional EV charging networks based on the Open Charge Point Protocol (OCPP) face challenges related to dynamic load management, cybersecurity, and efficient integration with renewable energy sources. This paper presents a novel AI-driven framework that integrates federated learning, predictive analytics, and real-time control within OCPP-compliant networks to enhance performance and sustainability. The proposed system utilizes edge AI modules at charging stations, supported by a central aggregator that employs federated learning to preserve data privacy while enabling network-wide optimization. A case study involving simulated smart charging stations demonstrates significant improvements, including an 18% reduction in peak load demand, a 29% increase in forecasting accuracy (MAPE of 8.5%), a 10% decrease in average charging wait times, and a 12% increase in on-site solar energy utilization. The framework’s compatibility with OCPP and related standards (e.g., IEC 61851, ISO 15118) ensures ease of deployment on existing infrastructure. These results indicate that the proposed AI-OCPP integration provides a scalable and intelligent foundation for next-generation EV charging networks that align with the goals of sustainable transportation and smart grid evolution.
The HER2-IHC-40x and HER2-IHC-40x-WSI datasets are high-resolution whole slide image (WSI) and patch-extracted region collection for HER2 immunohistochemistry (IHC) scoring in breast cancer pathology. 107 WSIs are scanned at 40 × magnification with Regions of Interest (ROIs) annotated by expert pathologists. Patches of 1024 × 1024 pixels are extracted from the ROIs and classified into four HER2 scores (0, 1+, 2+, 3+), yielding structured data for computational pathology analysis. There were two strategies of splitting: WSI-based split, where data was first split before extracting the patches and named as HER2-IHC-40x for this dataset, the other one is patch-based split, where patches were extracted first and then split, named as HER2-IHC-40x-WSI of this dataset. The filtering method for color histograms was applied to remove the non-tumour regions and artifacts, generating high-quality data. The dataset is applicable to deep learning applications, including HER2 classification and explainable AI. It is freely available on Zenodo, with preprocessing scripts provided via GitHub, enabling reproducibility in digital pathology research.
Background/Objectives: Estrogen receptor immunohistochemistry (ER-IHC) exhibits heterogeneous staining and substantial class imbalance, complicating segmentation of ordered expression categories. We evaluated whether class weighting, minority-focused crop sampling, adaptive minority curriculum (AMC), and Focal–Tversky optimization improved a common ResUNet-DS backbone for segmenting background/non-target pixels and C1 ER-negative, C2 weak-positive, C3 moderate-positive, and C4 strong-positive foreground categories. Methods: The dataset comprised 220 paired image–mask patches organized into 44 recovered five-patch source groups. A source-group-preserving nested five-fold design used outer folds of 45, 45, 45, 45, and 40 patches. Six controlled training conditions were compared, with four independently selected inner models ensembled for each condition and outer fold. Results: Unweighted random training achieved the best numerical mean for all five primary endpoints: foreground Dice (), C2–C4 Dice (), foreground IoU (), foreground quadratically weighted kappa (), and foreground-ordinal MAE (). Weighted random training was the strongest weighted/minority-sensitive condition but did not exceed the unweighted reference. None of 25 paired outer-fold comparisons reached ; the minimum raw p-value was , and all Holm-adjusted p-values were . A 20,000-replicate paired source-group bootstrap preserved the same overall ordering. Conclusions: More complex imbalance-handling strategies did not improve aggregate segmentation over unweighted training. Post hoc analyses showed scope-dependent probability quality and error ranking. IHC4BC provided expression-ordering consistency but not direct external segmentation validation. The findings support preliminary source-group-preserving methodological evidence rather than patient-level, whole-slide, or clinical validity.