Petagraph is a large-scale biomedical knowledge graph framework designed to integrate and analyze multi-omics biomolecular and biomedical data. It encompasses over 32 million nodes and 118 million relationships, leveraging more than 180 ontologies and standards from the Unified Biomedical Knowledge Graph (UBKG) to create a cohesive data environment for researchers.
Petagraph enhances the integration and analysis of multi-omics data through several mechanisms:
Petagraph's capabilities enable a variety of applications in biomedical research, including:
Future developments for Petagraph include enhancing automated validation techniques and integrating knowledge graphs with Large Language Models (LLMs) to improve biomedical data analysis. This integration could lead to more accurate and contextually relevant responses to complex biomedical queries, further advancing personalized medicine and clinical outcome predictions.
In summary, Petagraph represents a significant advancement in the integration and analysis of multi-omics and biomedical data. Its robust framework, extensive dataset integration, and advanced analytical capabilities position it as a valuable resource for the biomedical research community, enabling new discoveries and fostering a deeper understanding of complex biological systems.
from neo4j import GraphDatabase def query_petagraph(uri, user, password): driver = GraphDatabase.driver(uri, auth=(user, password)) with driver.session() as session: result = session.run("MATCH (g:Gene)-[r:ASSOCIATED_WITH]->(d:Disease) RETURN g.name, d.name LIMIT 10") for record in result: print(f'Gene: {record['g.name']}, Disease: {record['d.name']}') driver.close() # Example usage query_petagraph('bolt://localhost:7687', 'neo4j', 'password')