An Empirical Study of Causal Relation Extraction Transfer: Design and Data

We conduct an empirical analysis of neural network architectures and data transfer strategies for causal relation extraction. By conducting experiments with various contextual embedding layers and architectural components, we show that a relatively straightforward BioBERT-BiGRU relation extraction model generalizes better than other architectures across varying web-based sources and annotation strategies. Furthermore, we introduce a metric for evaluating transfer performance, $F1_{phrase}$ that emphasizes noun phrase localization rather than directly matching target tags. Using this metric, we can conduct data transfer experiments, ultimately revealing that augmentation with data with varying domains and annotation styles can improve performance. Data augmentation is especially beneficial when an adequate proportion of implicitly and explicitly causal sentences are included.

Advancing clinical trial outcomes using deep learning and predictive modelling: bridging precision medicine and patient-centered care

The integration of artificial intelligence [AI] into clinical trials has revolutionized the process of drug development and personalized medicine. Among these advancements, deep learning and predictive modelling have emerged as transformative tools for optimizing clinical trial design, patient recruitment, and real-time monitoring. This study explores the application of deep learning techniques, such as convolutional neural networks [CNNs] and transformerbased models, to stratify patients, forecast adverse events, and personalize treatment plans. Furthermore, predictive modelling approaches, including survival analysis and time-series forecasting, are employed to predict trial outcomes, enhancing efficiency and reducing trial failure rates. To address challenges in analysing unstructured clinical data, such as patient notes and trial protocols, natural language processing [NLP] techniques are utilized for extracting actionable insights. A custom dataset comprising structured patient demographics, genomic data, and unstructured text is curated for training and validating these models. Key metrics, including precision, recall, and F1 scores, are used to evaluate model performance, while trade-offs between accuracy and computational efficiency are examined to identify the optimal model for clinical deployment. This research underscores the potential of AI-driven methods to streamline clinical trial workflows, improve patient-centric outcomes, and reduce costs associated with trial inefficiencies. The findings provide a robust framework for integrating predictive analytics into precision medicine, paving the way for more adaptive and efficient clinical trials. By bridging the gap between technological innovation and real-world applications, this study contributes to advancing the role of AI in healthcare, particularly in fostering personalized care and improving overall trial success rates.