Paper List
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A Unified Variational Principle for Branching Transport Networks: Wave Impedance, Viscous Flow, and Tissue Metabolism
This paper solves the core problem of predicting the empirically observed branching exponent (α≈2.7) in mammalian arterial trees, which neither Murray...
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Household Bubbling Strategies for Epidemic Control and Social Connectivity
This paper addresses the core challenge of designing household merging (social bubble) strategies that effectively control epidemic risk while maximiz...
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Empowering Chemical Structures with Biological Insights for Scalable Phenotypic Virtual Screening
This paper addresses the core challenge of bridging the gap between scalable chemical structure screening and biologically informative but resource-in...
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A mechanical bifurcation constrains the evolution of cell sheet folding in the family Volvocaceae
This paper addresses the core problem of why there is an evolutionary gap in species with intermediate cell numbers (e.g., 256 cells) in Volvocaceae, ...
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Bayesian Inference in Epidemic Modelling: A Beginner’s Guide Illustrated with the SIR Model
This guide addresses the core challenge of estimating uncertain epidemiological parameters (like transmission and recovery rates) from noisy, real-wor...
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Geometric framework for biological evolution
This paper addresses the fundamental challenge of developing a coordinate-independent, geometric description of evolutionary dynamics that bridges gen...
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A multiscale discrete-to-continuum framework for structured population models
This paper addresses the core challenge of systematically deriving uniformly valid continuum approximations from discrete structured population models...
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Whole slide and microscopy image analysis with QuPath and OMERO
使QuPath能够直接分析存储在OMERO服务器中的图像而无需下载整个数据集,克服了大规模研究的本地存储限制。
Open Biomedical Knowledge Graphs at Scale: Construction, Federation, and AI Agent Access with Samyama Graph Database
VaidhyaMegha Private Limited, India
30秒速读
IN SHORT: This paper addresses the core pain point of fragmented biomedical data by constructing and federating large-scale, open knowledge graphs to enable seamless cross-domain queries and natural language access via AI agents.
核心创新
- Methodology A reproducible ETL pattern for constructing large-scale biomedical KGs from heterogeneous public sources, featuring cross-source deduplication, batch loading, and portable snapshot export.
- Methodology Demonstration of cross-KG federation via property-based joins, enabling queries that traverse multiple independent knowledge graphs (e.g., from clinical trials to biological pathways).
- Methodology Schema-driven MCP server generation that automatically exposes typed tools for LLM agents, achieving 98% accuracy on a new BiomedQA benchmark, significantly outperforming text-to-Cypher (0%) and standalone GPT-4o (75%).
主要结论
- The federated graph (7.9M nodes, 28M edges) loads in approximately 3 minutes on commodity hardware (AWS g4dn.4xlarge, 62 GB RAM), with cross-KG queries completing in 80 ms–4 s.
- Schema-driven MCP tools achieve 98% accuracy (39/40) on the BiomedQA benchmark, dramatically outperforming text-to-Cypher (0%) and standalone GPT-4o (75%).
- A Rust native loader constructs the Drug Interactions KG (32,726 nodes, 191,970 edges) in under 1 second, demonstrating orders-of-magnitude performance improvement over Python HTTP-based ETL.
摘要: Biomedical knowledge is fragmented across siloed databases—Reactome for pathways, STRING for protein interactions, Gene Ontology for functional annotations, ClinicalTrials.gov for study registries, DrugBank for drug vocabularies, DGIdb for drug–gene interactions, SIDER for side effects, and dozens more. Researchers routinely download flat files from each source and write bespoke scripts to cross-reference them, a process that is slow, error-prone, and not reproducible. We present three open-source biomedical knowledge graphs—Pathways KG (118,686 nodes, 834,785 edges from 5 sources), Clinical Trials KG (7,774,446 nodes, 26,973,997 edges from 5 sources), and Drug Interactions KG (32,726 nodes, 191,970 edges from 3 sources)—built on Samyama, a high-performance graph database written in Rust. Our contributions are threefold. First, we describe a reproducible ETL pattern for constructing large-scale KGs from heterogeneous public data sources, with cross-source deduplication, batch loading (both Python Cypher and Rust native loaders), and portable snapshot export. Second, we demonstrate cross-KG federation: loading all three snapshots into a single graph tenant enables property-based joins across datasets, answering questions like “For drugs indicated for diabetes, what are their gene targets and which biological pathways do those targets participate in?”—a query that no single KG can answer alone. Third, we introduce schema-driven MCP server generation: each KG automatically exposes typed tools for LLM agents via the Model Context Protocol, enabling natural-language access to graph queries. We evaluate domain-specific MCP tools against text-to-Cypher and standalone GPT-4o on a new BiomedQA benchmark (40 pharmacology questions), achieving 98% accuracy vs. 0% for text-to-Cypher and 75% for standalone GPT-4o. All data sources are open-license (CC BY 4.0, CC0, OBO, public domain). Snapshots, ETL code, and MCP configurations are publicly available. The combined federated graph (7.9M nodes, 28M edges) loads in approximately 3 minutes from portable snapshots on commodity cloud hardware (AWS g4dn.4xlarge, 62 GB RAM), and cross-KG queries complete in 80 ms–4 s.