This research discusses the critical need for early detection and treatment for early prediction of Freezing of Gaits (FOG) utilizing a wearable sensor technology powered with LoRa communication. The system consisted of an Esp-32 microcontroller, in which the trained model is utilized utilizing the Micromlgen Python library. The research investigates accurate FOG classification based on pertinent clinical data by utilizing machine learning (ML) algorithms like Catboost, XGBoost, and Extra Tree classifiers. The XGBoost could classify with approximately 97% accuracy, along with 96% for the catboost and 90% for the Extra Trees Classifier model. The SHAP analysis interpretability shows that GYR SI degree is the most affecting factor in the prediction of the diseases. These results show the possibility of monitoring and identifying the affected person with tracking location on GPS and providing aid as an assistive technology for aiding the affected. The developed sensor-based technology has great potential for real-world problem solving in the field of healthcare and biomedical technology enhancements.

Out-of-distribution (OOD) detection is crucial for ensuring the reliability and safety of machine learning models in real-world applications, where they frequently face data distributions unseen during training. Despite progress, existing methods are often vulnerable to spurious correlations that mislead models and compromise robustness. To address this, we propose SPROD, a novel prototype-based OOD detection approach that explicitly addresses the challenge posed by unknown spurious correlations. Our post-hoc method refines class prototypes to mitigate bias from spurious features without additional data or hyperparameter tuning, and is broadly applicable across diverse backbones and OOD detection settings. We conduct a comprehensive spurious correlation OOD detection benchmarking, comparing our method against existing approaches and demonstrating its superior performance across challenging OOD datasets, such as CelebA, Waterbirds, UrbanCars, Spurious Imagenet, and the newly introduced Animals MetaCoCo. On average, SPROD improves AUROC by 4.8% and FPR@95 by 9.4% over the second best.

This position paper argues that post-deployment monitoring in clinical AI is underdeveloped and proposes statistically valid and label-efficient testing frameworks as a principled foundation for ensuring reliability and safety in real-world deployment. A recent review found that only 9% of FDA-registered AI-based healthcare tools include a post-deployment surveillance plan. Existing monitoring approaches are often manual, sporadic, and reactive, making them ill-suited for the dynamic environments in which clinical models operate. We contend that post-deployment monitoring should be grounded in label-efficient and statistically valid testing frameworks, offering a principled alternative to current practices. We use the term "statistically valid" to refer to methods that provide explicit guarantees on error rates (e.g., Type I/II error), enable formal inference under pre-defined assumptions, and support reproducibility--features that align with regulatory requirements. Specifically, we propose that the detection of changes in the data and model performance degradation should be framed as distinct statistical hypothesis testing problems. Grounding monitoring in statistical rigor ensures a reproducible and scientifically sound basis for maintaining the reliability of clinical AI systems. Importantly, it also opens new research directions for the technical community--spanning theory, methods, and tools for statistically principled detection, attribution, and mitigation of post-deployment model failures in real-world settings.

Algorithmic fairness has emerged as a central issue in ML, and it has become standard practice to adjust ML algorithms so that they will satisfy fairness requirements such as Equal Opportunity. In this paper we consider the effects of adopting such fair classifiers on the overall level of ecosystem fairness. Specifically, we introduce the study of fairness with competing firms, and demonstrate the failure of fair classifiers in yielding fair ecosystems. Our results quantify the loss of fairness in systems, under a variety of conditions, based on classifiers' correlation and the level of their data overlap. We show that even if competing classifiers are individually fair, the ecosystem's outcome may be unfair; and that adjusting biased algorithms to improve their individual fairness may lead to an overall decline in ecosystem fairness. In addition to these theoretical results, we also provide supporting experimental evidence. Together, our model and results provide a novel and essential call for action.

The advent of single-cell Assay for Transposase-Accessible Chromatin using sequencing (scATAC-seq) offers an innovative perspective for deciphering regulatory mechanisms by assembling a vast repository of single-cell chromatin accessibility data. While foundation models have achieved significant success in single-cell transcriptomics, there is currently no foundation model for scATAC-seq that supports zero-shot high-quality cell identification and comprehensive multi-omics analysis simultaneously. Key challenges lie in the high dimensionality and sparsity of scATAC-seq data, as well as the lack of a standardized schema for representing open chromatin regions (OCRs). Here, we present ChromFound, a foundation model tailored for scATAC-seq. ChromFound utilizes a hybrid architecture and genome-aware tokenization to effectively capture genome-wide long contexts and regulatory signals from dynamic chromatin landscapes. Pretrained on 1.97 million cells from 30 tissues and 6 disease conditions, ChromFound demonstrates broad applicability across 6 diverse tasks. Notably, it achieves robust zero-shot performance in generating universal cell representations and exhibits excellent transferability in cell type annotation and cross-omics prediction. By uncovering enhancer-gene links undetected by existing computational methods, ChromFound offers a promising framework for understanding disease risk variants in the noncoding genome.

The identification of hope speech has become a promised NLP task, considering the need to detect motivational expressions of agency and goal-directed behaviour on social media platforms. This proposal evaluates traditional machine learning models and fine-tuned transformers for a previously split hope speech dataset as train, development and test set. On development test, a linear-kernel SVM and logistic regression both reached a macro-F1 of 0.78; SVM with RBF kernel reached 0.77, and Naïve Bayes hit 0.75. Transformer models delivered better results, the best model achieved weighted precision of 0.82, weighted recall of 0.80, weighted F1 of 0.79, macro F1 of 0.79, and 0.80 accuracy. These results suggest that while optimally configured traditional machine learning models remain agile, transformer architectures detect some subtle semantics of hope to achieve higher precision and recall in hope speech detection, suggesting that larges transformers and LLMs could perform better in small datasets.

We explore a "best-of-both" approach to modelling molecular properties by combining learned molecular descriptors from a graph neural network (GNN) with general-purpose descriptors and a mixed ensemble of machine learning (ML) models. We introduce a MetaModel framework to aggregate predictions from a diverse set of leading ML models. We present a featurisation scheme for combining task-specific GNN-derived features with conventional molecular descriptors. We demonstrate that our framework outperforms the cutting-edge ChemProp model on all regression datasets tested and 6 of 9 classification datasets. We further show that including the GNN features derived from ChemProp boosts the ensemble model's performance on several datasets where it otherwise would have underperformed. We conclude that to achieve optimal performance across a wide set of problems, it is vital to combine general-purpose descriptors with task-specific learned features and use a diverse set of ML models to make the predictions.

The increasing deployment of Machine Learning (ML) models in sensitive domains motivates the need for robust, practical privacy assessment tools. PrivacyGuard is a comprehensive tool for empirical differential privacy (DP) analysis, designed to evaluate privacy risks in ML models through state-of-the-art inference attacks and advanced privacy measurement techniques. To this end, PrivacyGuard implements a diverse suite of privacy attack -- including membership inference , extraction, and reconstruction attacks -- enabling both off-the-shelf and highly configurable privacy analyses. Its modular architecture allows for the seamless integration of new attacks, and privacy metrics, supporting rapid adaptation to emerging research advances. We make PrivacyGuard available at https://github.com/facebookresearch/PrivacyGuard.

This thesis works to address a pivotal challenge in medical image analysis: the reliance on extensive labeled datasets, which are often limited due to the need for expert annotation and constrained by privacy and legal issues. By focusing on the development of self-supervised learning techniques and domain adaptation methods, this research aims to circumvent these limitations, presenting a novel approach to enhance the utility and efficacy of deep learning in medical imaging. Central to this thesis is the development of the Medformer, an innovative neural network architecture designed for multitask learning and deep domain adaptation. This model is adept at pre-training on diverse medical image datasets, handling varying sizes and modalities, and is equipped with a dynamic input-output adaptation mechanism. This enables efficient processing and integration of a wide range of medical image types, from 2D X-rays to complex 3D MRIs, thus mitigating the dependency on large labeled datasets. Further, the thesis explores the current state of self-supervised learning in medical imaging. It introduces novel pretext tasks that are capable of extracting meaningful information from unlabeled data, significantly advancing the model's interpretative abilities. This approach is validated through rigorous experimentation, including the use of the MedMNIST dataset, demonstrating the model's proficiency in learning generalized features applicable to various downstream tasks. In summary, this thesis contributes to the advancement of medical image analysis by offering a scalable, adaptable framework that reduces reliance on labeled data. It paves the way for more accurate, efficient diagnostic tools in healthcare, signifying a major step forward in the application of deep learning in medical imaging.

We introduce the task of Multi-Modal Context-Aware Recognition (MCoRec) in the ninth CHiME Challenge, which addresses the cocktail-party problem of overlapping conversations in a single-room setting using audio, visual, and contextual cues. MCoRec captures natural multi-party conversations where the recordings focus on unscripted, casual group chats, leading to extreme speech overlap of up to 100% and highly fragmented conversational turns. The task requires systems to answer the question "Who speaks when, what, and with whom?" by jointly transcribing each speaker's speech and clustering them into their respective conversations from audio-visual recordings. Audio-only baselines exceed 100% word error rate, whereas incorporating visual cues yields substantial 50% improvements, highlighting the importance of multi-modality. In this manuscript, we present the motivation behind the task, outline the data collection process, and report the baseline systems developed for the MCoRec.