A key feature differentiating artificial general intelligence (AGI) from traditional AI is that AGI can perform composite tasks that require a wide range of capabilities. Although embodied agents powered by multimodal large language models (MLLMs) offer rich perceptual and interactive capabilities, it remains largely unexplored whether they can solve composite tasks. In the current work, we designed a set of composite tasks inspired by common daily activities observed in early childhood development. Within a dynamic and simulated home environment, these tasks span three core domains: object understanding, spatial intelligence, and social activity. We evaluated 17 leading proprietary and open-source MLLMs on these tasks. The results consistently showed poor performance across all three domains, indicating a substantial gap between current capabilities and general intelligence requirements. Together, our tasks offer a preliminary framework for evaluating the general capabilities of embodied agents, marking an early but significant step toward the development of embodied MLLMs and their real-world deployment.

Experimental studies of beauty hadron decays face significant challenges due to a wide range of backgrounds arising from the numerous possible decay channels with similar final states. For a particular signal decay, the process for ascertaining the most relevant background processes necessitates a detailed analysis of final state particles, potential misidentifications, and kinematic overlaps, which, due to computational limitations, is restricted to the simulation of only the most relevant backgrounds. Moreover, this process typically relies on the physicist's intuition and expertise, as no systematic method exists. This paper has two primary goals. First, from a particle physics perspective, we present a novel approach that utilises Reinforcement Learning (RL) to overcome the aforementioned challenges by systematically determining the critical backgrounds affecting beauty hadron decay measurements. While beauty hadron physics serves as the case study in this work, the proposed strategy is broadly adaptable to other types of particle physics measurements. Second, from a Machine Learning perspective, we introduce a novel algorithm which exploits the synergy between RL and Genetic Algorithms (GAs) for environments with highly sparse rewards and a large trajectory space. This strategy leverages GAs to efficiently explore the trajectory space and identify successful trajectories, which are used to guide the RL agent's training. Our method also incorporates a transformer architecture for the RL agent to handle token sequences representing decays.

Frontier AI systems require governance mechanisms that can verify internal alignment, not just behavioral compliance. Private governance mechanisms audits, certification, insurance, and procurement are emerging to complement public regulation, but they require technical substrates that generate verifiable causal evidence about model behavior. This paper argues that mechanistic interpretability provides this substrate. We frame interpretability not as post-hoc explanation but as a design constraint embedding auditability, provenance, and bounded transparency within model architectures. Integrating causal abstraction theory and empirical benchmarks such as MIB and LoBOX, we outline how interpretability-first models can underpin private assurance pipelines and role-calibrated transparency frameworks. This reframing situates interpretability as infrastructure for private AI governance bridging the gap between technical reliability and institutional accountability.

Imagine a world where clinical trials need far fewer patients to achieve the same statistical power, thanks to the knowledge encoded in large language models (LLMs). We present a novel framework for hierarchical Bayesian modeling of adverse events in multi-center clinical trials, leveraging LLM-informed prior distributions. Unlike data augmentation approaches that generate synthetic data points, our methodology directly obtains parametric priors from the model. Our approach systematically elicits informative priors for hyperparameters in hierarchical Bayesian models using a pre-trained LLM, enabling the incorporation of external clinical expertise directly into Bayesian safety modeling. Through comprehensive temperature sensitivity analysis and rigorous cross-validation on real-world clinical trial data, we demonstrate that LLM-derived priors consistently improve predictive performance compared to traditional meta-analytical approaches. This methodology paves the way for more efficient and expert-informed clinical trial design, enabling substantial reductions in the number of patients required to achieve robust safety assessment and with the potential to transform drug safety monitoring and regulatory decision making.

Deep learning models often learn and exploit spurious correlations in training data, using these non-target features to inform their predictions. Such reliance leads to performance degradation and poor generalization on unseen data. To address these limitations, we introduce a more general form of counterfactual data augmentation, termed counterbias data augmentation, which simultaneously tackles multiple biases (e.g., gender bias, simplicity bias) and enhances out-of-distribution robustness. We present CoBA: CounterBias Augmentation, a unified framework that operates at the semantic triple level: first decomposing text into subject-predicate-object triples, then selectively modifying these triples to disrupt spurious correlations. By reconstructing the text from these adjusted triples, CoBA generates counterbias data that mitigates spurious patterns. Through extensive experiments, we demonstrate that CoBA not only improves downstream task performance, but also effectively reduces biases and strengthens out-of-distribution resilience, offering a versatile and robust solution to the challenges posed by spurious correlations.

Quantization offers a practical solution to deploy LLMs in resource-constraint environments. However, its impact on internal representations remains understudied, raising questions about the reliability of quantized models. In this study, we employ a range of interpretability techniques to investigate how quantization affects model and neuron behavior. We analyze multiple LLMs under 4-bit and 8-bit quantization. Our findings reveal that the impact of quantization on model calibration is generally minor. Analysis of neuron activations indicates that the number of dead neurons, i.e., those with activation values close to 0 across the dataset, remains consistent regardless of quantization. In terms of neuron contribution to predictions, we observe that smaller full precision models exhibit fewer salient neurons, whereas larger models tend to have more, with the exception of Llama-2-7B. The effect of quantization on neuron redundancy varies across models. Overall, our findings suggest that effect of quantization may vary by model and tasks, however, we did not observe any drastic change which may discourage the use of quantization as a reliable model compression technique.

Ensuring the robustness of factual knowledge in LLMs is critical for reliable applications in tasks such as question answering and reasoning. However, existing evaluation methods predominantly focus on performance-based metrics, often investigating from the perspective of prompt perturbations, which captures only the externally triggered side of knowledge robustness. To bridge this gap, we introduce a principled approach to measure factual robustness from the perspective of the generation process by analyzing token distribution entropy in combination with temperature scaling sensitivity. These two factors build the Factual Robustness Score (FRS), a novel metric which quantifies the stability of a fact against perturbations in decoding conditions, given its initial uncertainty. To validate our approach, we conduct extensive experiments on 5 LLMs across 3 closed-book QA datasets (SQuAD, TriviaQA, and HotpotQA). We show that factual robustness varies significantly -- smaller models report an FRS of $0.76$, larger ones $0.93$ -- with accuracy degrading by ~$60\%$ under increased uncertainty. These insights demonstrate how entropy and temperature scaling impact factual accuracy, and lay a foundation for developing more robust knowledge retention and retrieval in future models.

Graph machine learning has been widely explored in various domains, such as community detection, transaction analysis, and recommendation systems. In these applications, anomaly detection plays an important role. Recently, studies have shown that anomalies on graphs induce spectral shifts. Some supervised methods have improved the utilization of such spectral domain information. However, they remain limited by the scarcity of labeled data due to the nature of anomalies. On the other hand, existing unsupervised learning approaches predominantly rely on spatial information or only employ low-pass filters, thereby losing the capacity for multi-band analysis. In this paper, we propose Graph Autoencoder with Spectral Encoder and Spectral Decoder (GRASPED) for node anomaly detection. Our unsupervised learning model features an encoder based on Graph Wavelet Convolution, along with structural and attribute decoders. The Graph Wavelet Convolution-based encoder, combined with a Wiener Graph Deconvolution-based decoder, exhibits bandpass filter characteristics that capture global and local graph information at multiple scales. This design allows for a learning-based reconstruction of node attributes, effectively capturing anomaly information. Extensive experiments on several real-world graph anomaly detection datasets demonstrate that GRASPED outperforms current state-of-the-art models.

Designing therapeutic peptides with tailored properties is hindered by the vastness of sequence space, limited experimental data, and poor interpretability of current generative models. To address these challenges, we introduce PepThink-R1, a generative framework that integrates large language models (LLMs) with chain-of-thought (CoT) supervised fine-tuning and reinforcement learning (RL). Unlike prior approaches, PepThink-R1 explicitly reasons about monomer-level modifications during sequence generation, enabling interpretable design choices while optimizing for multiple pharmacological properties. Guided by a tailored reward function balancing chemical validity and property improvements, the model autonomously explores diverse sequence variants. We demonstrate that PepThink-R1 generates cyclic peptides with significantly enhanced lipophilicity, stability, and exposure, outperforming existing general LLMs (e.g., GPT-5) and domain-specific baseline in both optimization success and interpretability. To our knowledge, this is the first LLM-based peptide design framework that combines explicit reasoning with RL-driven property control, marking a step toward reliable and transparent peptide optimization for therapeutic discovery.

As large language models (LLMs) are increasingly deployed in real-world applications, the need to selectively remove unwanted knowledge while preserving model utility has become paramount. Recent work has explored sparse autoencoders (SAEs) to perform precise interventions on monosemantic features. However, most SAE-based methods operate at inference time, which does not create persistent changes in the model's parameters. Such interventions can be bypassed or reversed by malicious actors with parameter access. We introduce CRISP, a parameter-efficient method for persistent concept unlearning using SAEs. CRISP automatically identifies salient SAE features across multiple layers and suppresses their activations. We experiment with two LLMs and show that our method outperforms prior approaches on safety-critical unlearning tasks from the WMDP benchmark, successfully removing harmful knowledge while preserving general and in-domain capabilities. Feature-level analysis reveals that CRISP achieves semantically coherent separation between target and benign concepts, allowing precise suppression of the target features.