An open research community dedicated to unlocking the therapeutic potential of existing drugs for patients with rare and complex diseases. We advance precision medicine through the integration of Electronic Health Records, Knowledge Graphs, Multi-Omics Data, and Deep Learning Models.
We focus on rare and complex diseases such as ME/CFS, Long Covid, ALS, and more, leveraging cutting-edge technologies to accelerate drug discovery and precision medicine.
Integrate and analyze electronic health records to understand patient phenotypes, disease progression, and treatment outcomes for rare and complex diseases.
Curate and analyze multi-omics data from public databases and literature for rare and complex diseases, enabling comprehensive molecular profiling and biomarker discovery.
Build comprehensive biomedical knowledge graphs for drug repurposing and disease mechanism understanding, connecting genes, drugs, diseases, and molecular pathways.
Develop advanced AI models that integrate multi-omics data and knowledge graphs to predict drug candidates and understand disease mechanisms for rare and complex diseases.
Open-source platforms and tools developed by our community for drug discovery, data analysis, and precision medicine research.
Comprehensive drug and target databases with advanced search and analysis tools for drug repurposing research.
Database Explore Database →Multi-omics data analysis platforms and quality control tools for comprehensive molecular profiling.
Analysis View Tools →Multi-agent systems and AI tools for automated biomedical research and knowledge discovery.
AI Tools Explore AI Tools →Meet the researchers and developers behind OpenProphetDB, working across prestigious institutions worldwide.
We are looking for partners who are highly motivated on drug repurposing to join the OpenProphetDB community. Let's work together to unlock the therapeutic potential of existing drugs for patients with rare and complex diseases.