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William J. Richardson

Publications and source records attributed to William J. Richardson.

3 recordsLinked to original sources

RAG-GNN: Integrating Retrieved Knowledge with Graph Neural Networks for Precision Medicine

Network topology excels at structural predictions but fails to capture functional semantics encoded in biomedical literature. We present RAG-GNN, an end-to-end trainable retrieval-augmented graph neural network framework that integrates GNN representations with dynamically retrieved literature-derived knowledge through a jointly optimized retrieval projection, gated fusion mechanism, and contrastive alignment. In a cancer signaling case study (379 proteins, 3,498 interactions, 14 functional categories), RAG-GNN improves functional clustering from silhouette $= -0.237 \pm 0.065$ (GNN-only) to $-0.144 \pm 0.066$, a consistent improvement of $+0.093 \pm 0.022$ across 10 random seeds, while the learned retrieval achieves mean precision@10 $= 0.242$, a 152\% improvement over the random baseline ($0.096$). Heuristic information decomposition with bootstrap confidence intervals reveals that topology and retrieval encode overwhelmingly shared information (95.6\%), with retrieval improving both intra-cluster cohesion (silhouette) and cluster agreement (ARI $+0.021 \pm 0.015$). Counterfactual experiments confirm that adversarial, absent, and random retrieval all degrade performance, validating that the gated fusion mechanism depends on document content. Benchmarking against eight established embedding methods demonstrates task-specific complementarity: topology-focused methods achieve strong link prediction, while retrieval augmentation consistently improves functional clustering within the controlled GNN-only ablation. DDR1 subnetwork analysis provides confirmatory validation consistent with established synthetic lethality relationships. These results establish that topology-only and retrieval-augmented approaches serve complementary purposes for precision medicine applications.

q-bio.MN↗

ECMSim: A high-performance interactive web application for real-time spatiotemporal simulation of cardiac ECM signaling and diffusion

Extracellular matrix (ECM) remodeling is central to a wide variety of healthy and diseased tissue processes. Unfortunately, predicting ECM remodeling under various chemical and mechanical conditions has proven to be excessively challenging, due in part to its complex regulation by intracellular and extracellular molecular reaction networks that are spatially and temporally dynamic. We introduce ECMSim, which is a highly interactive, real-time, and web application designed to simulate heterogeneous matrix remodeling. The current model simulates cardiac scar tissue with configurable input conditions using a large-scale model of the cardiac fibroblast signaling network. Cardiac fibrosis is a major component of many forms of heart failure. ECMSim solves 1.37 million coupled ordinary differential equations (ODEs) and executes approximately 4.84 million operations per time step in real time, encompassing 137 molecular species and 259 regulatory interactions per cell across a 100x100 spatial array (10,000 cells), which accounts for inputs, receptors, intracellular signaling cascades, ECM production, feedback loops, and molecular diffusion. The algorithm is represented by a set of ODEs that are coupled with ECM molecular diffusion. The equations are solved on demand using compiled C++ and the WebAssembly standard. The software enables the investigation of pathological or experimental conditions, hypothetical scenarios, matrix remodeling, or the testing of the effects of an experimental drug(s) with a target receptor.

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Hierarchical Molecular Language Models (HMLMs)

Artificial intelligence (AI) is reshaping computational and network biology by enabling new approaches to decode cellular communication networks. We introduce Hierarchical Molecular Language Models (HMLMs), a novel framework that models cellular signaling as a specialized molecular language, where signaling molecules function as tokens, protein interactions define syntax, and functional consequences constitute semantics. HMLMs employ a transformer-based architecture adapted to accommodate graph-structured signaling networks through information transducers, mathematical entities that capture how molecules receive, process, and transmit signals. The architecture integrates multi-modal data sources across molecular, pathway, and cellular scales through hierarchical attention mechanisms and scale-bridging operators that enable information flow across biological hierarchies. Applied to a complex network of cardiac fibroblast signaling, HMLMs outperformed traditional approaches in temporal dynamics prediction, particularly under sparse sampling conditions. Attention-based analysis revealed biologically meaningful crosstalk patterns, including previously uncharacterized interactions between signaling pathways. By bridging molecular mechanisms with cellular phenotypes through AI-driven molecular language representation, HMLMs establish a foundation for biology-oriented large language models (LLMs) that could be pre-trained on comprehensive pathway datasets and applied across diverse signaling systems and tissues, advancing precision medicine and therapeutic discovery.

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