Understanding and mitigating biases is critical for the adoption of large language models (LLMs) in high-stakes decision-making. We introduce Admissions and Hiring, decision tasks with hypothetical applicant profiles where a person's race can be inferred from their name, as simplified test beds for racial bias. We show that Gemma 2B Instruct and LLaMA 3.2 3B Instruct exhibit strong biases. Gemma grants admission to 26% more White than Black applicants, and LLaMA hires 60% more Asian than White applicants. We demonstrate that these biases are resistant to prompt engineering: multiple prompting strategies all fail to promote fairness. In contrast, using distributed alignment search, we can identify "race subspaces" within model activations and intervene on them to debias model decisions. Averaging the representation across all races within the subspaces reduces Gemma's bias by 37-57%. Finally, we examine the generalizability of Gemma's race subspaces, and find limited evidence for generalization, where changing the prompt format can affect the race representation. Our work suggests mechanistic approaches may provide a promising venue for improving the fairness of LLMs, but a universal race representation remains elusive.

As a developing country, Fiji is facing rapid urbanisation, which is visible in the massive development projects that include housing, roads, and civil works. In this study, we present machine learning and remote sensing frameworks to compare land use and land cover change from 2013 to 2024 in Nadi, Fiji. The ultimate goal of this study is to provide technical support in land cover/land use modelling and change detection. We used Landsat-8 satellite image for the study region and created our training dataset with labels for supervised machine learning. We used Google Earth Engine and unsupervised machine learning via k-means clustering to generate the land cover map. We used convolutional neural networks to classify the selected regions' land cover types. We present a visualisation of change detection, highlighting urban area changes over time to monitor changes in the map.

Drug-drug interactions (DDIs) represent a critical challenge in pharmacology, often leading to adverse drug reactions with significant implications for patient safety and healthcare outcomes. While graph-based methods have achieved strong predictive performance, most approaches treat drug pairs independently, overlooking the complex, context-dependent interactions unique to drug pairs. Additionally, these models struggle to integrate biological interaction networks and molecular-level structures to provide meaningful mechanistic insights. In this study, we propose MolecBioNet, a novel graph-based framework that integrates molecular and biomedical knowledge for robust and interpretable DDI prediction. By modeling drug pairs as unified entities, MolecBioNet captures both macro-level biological interactions and micro-level molecular influences, offering a comprehensive perspective on DDIs. The framework extracts local subgraphs from biomedical knowledge graphs and constructs hierarchical interaction graphs from molecular representations, leveraging classical graph neural network methods to learn multi-scale representations of drug pairs. To enhance accuracy and interpretability, MolecBioNet introduces two domain-specific pooling strategies: context-aware subgraph pooling (CASPool), which emphasizes biologically relevant entities, and attention-guided influence pooling (AGIPool), which prioritizes influential molecular substructures. The framework further employs mutual information minimization regularization to enhance information diversity during embedding fusion. Experimental results demonstrate that MolecBioNet outperforms state-of-the-art methods in DDI prediction, while ablation studies and embedding visualizations further validate the advantages of unified drug pair modeling and multi-scale knowledge integration.

Regional discrimination is a persistent social issue in Vietnam. While existing research has explored hate speech in the Vietnamese language, the specific issue of regional discrimination remains under-addressed. Previous studies primarily focused on model development without considering practical system implementation. In this work, we propose a task called Detection of Regional Discriminatory Comments on Vietnamese Social Media, leveraging the power of machine learning and transfer learning models. We have built the ViRDC (Vietnamese Regional Discrimination Comments) dataset, which contains comments from social media platforms, providing a valuable resource for further research and development. Our approach integrates streaming capabilities to process real-time data from social media networks, ensuring the system's scalability and responsiveness. We developed the system on the Apache Spark framework to efficiently handle increasing data inputs during streaming. Our system offers a comprehensive solution for the real-time detection of regional discrimination in Vietnam.

Vietnamese, a low-resource language, is typically categorized into three primary dialect groups that belong to Northern, Central, and Southern Vietnam. However, each province within these regions exhibits its own distinct pronunciation variations. Despite the existence of various speech recognition datasets, none of them has provided a fine-grained classification of the 63 dialects specific to individual provinces of Vietnam. To address this gap, we introduce Vietnamese Multi-Dialect (ViMD) dataset, a novel comprehensive dataset capturing the rich diversity of 63 provincial dialects spoken across Vietnam. Our dataset comprises 102.56 hours of audio, consisting of approximately 19,000 utterances, and the associated transcripts contain over 1.2 million words. To provide benchmarks and simultaneously demonstrate the challenges of our dataset, we fine-tune state-of-the-art pre-trained models for two downstream tasks: (1) Dialect identification and (2) Speech recognition. The empirical results suggest two implications including the influence of geographical factors on dialects, and the constraints of current approaches in speech recognition tasks involving multi-dialect speech data. Our dataset is available for research purposes.

The field of drug discovery has experienced a remarkable transformation with the advent of artificial intelligence (AI) and machine learning (ML) technologies. However, as these AI and ML models are becoming more complex, there is a growing need for transparency and interpretability of the models. Explainable Artificial Intelligence (XAI) is a novel approach that addresses this issue and provides a more interpretable understanding of the predictions made by machine learning models. In recent years, there has been an increasing interest in the application of XAI techniques to drug discovery. This review article provides a comprehensive overview of the current state-of-the-art in XAI for drug discovery, including various XAI methods, their application in drug discovery, and the challenges and limitations of XAI techniques in drug discovery. The article also covers the application of XAI in drug discovery, including target identification, compound design, and toxicity prediction. Furthermore, the article suggests potential future research directions for the application of XAI in drug discovery. The aim of this review article is to provide a comprehensive understanding of the current state of XAI in drug discovery and its potential to transform the field.

The availability of multi-modality datasets provides a unique opportunity to characterize the same object of interest using multiple viewpoints more comprehensively. In this work, we investigate the use of canonical correlation analysis (CCA) and penalized variants of CCA (pCCA) for the fusion of two modalities. We study a simple graphical model for the generation of two-modality data. We analytically show that, with known model parameters, posterior mean estimators that jointly use both modalities outperform arbitrary linear mixing of single modality posterior estimators in latent variable prediction. Penalized extensions of CCA (pCCA) that incorporate domain knowledge can discover correlations with high-dimensional, low-sample data, whereas traditional CCA is inapplicable. To facilitate the generation of multi-dimensional embeddings with pCCA, we propose two matrix deflation schemes that enforce desirable properties exhibited by CCA. We propose a two-stage prediction pipeline using pCCA embeddings generated with deflation for latent variable prediction by combining all the above. On simulated data, our proposed model drastically reduces the mean-squared error in latent variable prediction. When applied to publicly available histopathology data and RNA-sequencing data from The Cancer Genome Atlas (TCGA) breast cancer patients, our model can outperform principal components analysis (PCA) embeddings of the same dimension in survival prediction.