The reliance of organisations on computer networks is enabled by network programmability, which is typically achieved through Service Function Chaining. These chains virtualise network functions, link them, and programmatically embed them on networking infrastructure. Optimal embedding of Service Function Chains is an NP-hard problem, with three sub-problems, chain composition, virtual network function embedding, and link embedding, that have to be optimised simultaneously, rather than sequentially, for optimal results. Genetic Algorithms have been employed for this, but existing approaches either do not optimise all three sub-problems or do not optimise all three sub-problems simultaneously. We propose a Genetic Algorithm-based approach called GENESIS, which evolves three sine-function-activated Neural Networks, and funnels their output to a Gaussian distribution and an A* algorithm to optimise all three sub-problems simultaneously. We evaluate GENESIS on an emulator across 48 different data centre scenarios and compare its performance to two state-of-the-art Genetic Algorithms and one greedy algorithm. GENESIS produces an optimal solution for 100% of the scenarios, whereas the second-best method optimises only 71% of the scenarios. Moreover, GENESIS is the fastest among all Genetic Algorithms, averaging 15.84 minutes, compared to an average of 38.62 minutes for the second-best Genetic Algorithm.

As large language model (LLM) agents increasingly automate complex web tasks, they boost productivity while simultaneously introducing new security risks. However, relevant studies on web agent attacks remain limited. Existing red-teaming approaches mainly rely on manually crafted attack strategies or static models trained offline. Such methods fail to capture the underlying behavioral patterns of web agents, making it difficult to generalize across diverse environments. In web agent attacks, success requires the continuous discovery and evolution of attack strategies. To this end, we propose Genesis, a novel agentic framework composed of three modules: Attacker, Scorer, and Strategist. The Attacker generates adversarial injections by integrating the genetic algorithm with a hybrid strategy representation. The Scorer evaluates the target web agent's responses to provide feedback. The Strategist dynamically uncovers effective strategies from interaction logs and compiles them into a continuously growing strategy library, which is then re-deployed to enhance the Attacker's effectiveness. Extensive experiments across various web tasks show that our framework discovers novel strategies and consistently outperforms existing attack baselines.

A central challenge in cognitive neuroscience is to explain how semantic and episodic memory, two major forms of declarative memory, typically associated with cortical and hippocampal processing, interact to support learning, recall, and imagination. Despite significant advances, we still lack a unified computational framework that jointly accounts for core empirical phenomena across both semantic and episodic processing domains. Here, we introduce the Generative Episodic-Semantic Integration System (GENESIS), a computational model that formalizes memory as the interaction between two limited-capacity generative systems: a Cortical-VAE, supporting semantic learning and generalization, and a Hippocampal-VAE, supporting episodic encoding and retrieval within a retrieval-augmented generation (RAG) architecture. GENESIS reproduces hallmark behavioral findings, including generalization in semantic memory, recognition, serial recall effects and gist-based distortions in episodic memory, and constructive episodic simulation, while capturing their dynamic interactions. The model elucidates how capacity constraints shape the fidelity and memorability of experiences, how semantic processing introduces systematic distortions in episodic recall, and how episodic replay can recombine previous experiences. Together, these results provide a principled account of memory as an active, constructive, and resource-bounded process. GENESIS thus advances a unified theoretical framework that bridges semantic and episodic memory, offering new insights into the generative foundations of human cognition.

Image captioning, situated at the intersection of computer vision and natural language processing, requires a sophisticated understanding of both visual scenes and linguistic structure. While modern approaches are dominated by large-scale Transformer architectures, this paper documents a systematic, iterative development of foundational image captioning models, progressing from a simple CNN-LSTM encoder-decoder to a competitive attention-based system. This paper presents a series of five models, beginning with Genesis and concluding with Nexus, an advanced model featuring an EfficientNetV2B3 backbone and a dynamic attention mechanism. The experiments chart the impact of architectural enhancements and demonstrate a key finding within the classic CNN-LSTM paradigm: merely upgrading the visual backbone without a corresponding attention mechanism can degrade performance, as the single-vector bottleneck cannot transmit the richer visual detail. This insight validates the architectural shift to attention. Trained on the MS COCO 2017 dataset, the final model, Nexus, achieves a BLEU-4 score of 31.4, surpassing several foundational benchmarks and validating the iterative design process. This work provides a clear, replicable blueprint for understanding the core architectural principles that underpin modern vision-language tasks.

Causal discovery in multi-omic datasets is crucial for understanding the bigger picture of gene regulatory mechanisms, but remains challenging due to high dimensionality, differentiation of direct from indirect relationships, and hidden confounders. We introduce GENESIS (GEne Network inference from Expression SIgnals and SNPs), a constraint-based algorithm that leverages the natural causal precedence of genotypes to infer ancestral relationships in transcriptomic data. Unlike traditional causal discovery methods that start with a fully connected graph, GENESIS initialises an empty ancestrality matrix and iteratively populates it with direct, indirect or non-causal relationships using a series of provably sound marginal and conditional independence tests. By integrating genotypes as fixed causal anchors, GENESIS provides a principled ``head start'' to classical causal discovery algorithms, restricting the search space to biologically plausible edges. We test GENESIS on synthetic and real-world genomic datasets. This framework offers a powerful avenue for uncovering causal pathways in complex traits, with promising applications to functional genomics, drug discovery, and precision medicine.

The cutting edge of applying AI to science is the closed-loop automation of scientific research: robot scientists. We have previously developed two robot scientists: `Adam' (for yeast functional biology), and `Eve' (for early-stage drug design)). We are now developing a next generation robot scientist Genesis. With Genesis we aim to demonstrate that an area of science can be investigated using robot scientists unambiguously faster, and at lower cost, than with human scientists. Here we report progress on the Genesis project. Genesis is designed to automatically improve system biology models with thousands of interacting causal components. When complete Genesis will be able to initiate and execute in parallel one thousand hypothesis-led closed-loop cycles of experiment per-day. Here we describe the core Genesis hardware: the one thousand computer-controlled $\mu$-bioreactors. For the integrated Mass Spectrometry platform we have developed AutonoMS, a system to automatically run, process, and analyse high-throughput experiments. We have also developed Genesis-DB, a database system designed to enable software agents access to large quantities of structured domain information. We have developed RIMBO (Revisions for Improvements of Models in Biology Ontology) to describe the planned hundreds of thousands of changes to the models. We have demonstrated the utility of this infrastructure by developed two relational learning bioinformatic projects. Finally, we describe LGEM+ a relational learning system for the automated abductive improvement of genome-scale metabolic models.