William Borges Domingues

Mihaela Gaman, Adrian-Gabriel Chifu, William Domingues et al.

We present a novel corpus for French dialect identification comprising 413,522 French text samples collected from public news websites in Belgium, Canada, France and Switzerland. To ensure an accurate estimation of the dialect identification performance of models, we designed the corpus to eliminate potential biases related to topic, writing style, and publication source. More precisely, the training, validation and test splits are collected from different news websites, while searching for different keywords (topics). This leads to a French cross-domain (FreCDo) dialect identification task. We conduct experiments with four competitive baselines, a fine-tuned CamemBERT model, an XGBoost based on fine-tuned CamemBERT features, a Support Vector Machines (SVM) classifier based on fine-tuned CamemBERT features, and an SVM based on word n-grams. Aside from presenting quantitative results, we also make an analysis of the most discriminative features learned by CamemBERT. Our corpus is available at https://github.com/MihaelaGaman/FreCDo.

Paulo R. Ferreira, Lucas Coutinho Freitas, Laís dos Santos Gonçalves et al.

NA methylation profiling has become a powerful approach for central nervous system (CNS) tumor classification, yet important challenges remain regarding cross-cohort transferability, methodological correctness, and robust multiclass evaluation. In this work, we propose a novel and methodologically rigorous machine-learning approach for methylation-based CNS tumor classification that combines Sparse Random Projection for dimensionality reduction with multinomial logistic regression for classification. We evaluate the proposed approach in the same general experimental setting established by a widely used reference classifier. On the 2,801-sample reference cohort, our method achieves a mean accuracy of 96\% under stratified 3-fold cross-validation. On the independent 1,104-sample clinical evaluation cohort, it reaches 86\% accuracy at the 91-class level and 93\% when predictions are evaluated at the methylation class family level. These results improve upon the corresponding state-of-the-art reference figures of 82\% class-level concordance and 88\% family-level concordance, yielding absolute gains of approximately 4 and 5 percentage points, respectively. This improvement is clinically relevant: in a diagnostic setting, a 5-point increase in correct tumor classification can directly affect cancer subtype assignment and, in turn, influence treatment selection and downstream clinical decision-making. Our results show that the proposed model, grounded in stronger methodological practice in machine learning, consistently outperforms the previous state of the art across evaluation settings and can materially improve the reliability of CNS tumor classification.