CancerAtHomeV2 / CHANGELOG.md
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# Changelog
All notable changes to Cancer@Home v2 will be documented in this file.
## [2.0.0] - 2025-11-19
### πŸŽ‰ Initial Release
#### Added
- **Core Infrastructure**
- FastAPI backend with REST and GraphQL APIs
- Neo4j graph database integration
- Docker Compose setup for easy deployment
- Python virtual environment configuration
- Comprehensive YAML-based configuration system
- **BOINC Integration**
- Distributed computing task submission
- Task status monitoring and tracking
- Support for variant calling, BLAST, and alignment tasks
- Task statistics and performance metrics
- JSON-based task persistence
- **GDC Data Portal Integration**
- API client for GDC cancer data
- File search and download capabilities
- Support for TCGA and TARGET projects
- MAF and VCF file parsers
- Clinical data extraction
- **Bioinformatics Pipeline**
- FASTQ quality control and filtering
- Adapter trimming
- BLAST sequence alignment (BLASTN/BLASTP)
- Variant calling from sequencing data
- Cancer variant identification
- Tumor mutation burden calculation
- **Neo4j Graph Database**
- Comprehensive graph schema (Genes, Mutations, Patients, Cancer Types)
- Repository pattern for data access
- GraphQL schema with flexible querying
- Sample dataset with 7 genes, 5 mutations, 5 patients, 4 cancer types
- Optimized with constraints and indexes
- **Web Dashboard**
- Modern, responsive HTML5/CSS3/JavaScript interface
- 5 main sections: Dashboard, Neo4j Visualization, BOINC Tasks, GDC Data, Pipeline
- Interactive D3.js graph visualization
- Chart.js analytics and statistics
- Real-time data updates
- Clean gradient-based design
- **API Endpoints**
- `/api/health` - System health check
- `/api/neo4j/summary` - Database statistics
- `/api/neo4j/genes/{symbol}` - Gene information
- `/api/boinc/*` - BOINC task management
- `/api/gdc/*` - GDC data access
- `/api/pipeline/*` - Bioinformatics tools
- `/graphql` - GraphQL playground
- `/docs` - Swagger API documentation
- **Documentation**
- Comprehensive README with installation guide
- Quick start guide (QUICKSTART.md)
- Detailed user guide (USER_GUIDE.md)
- GraphQL query examples (GRAPHQL_EXAMPLES.md)
- Architecture documentation (ARCHITECTURE.md)
- Project summary (PROJECT_SUMMARY.md)
- MIT License
- **Setup & Deployment**
- Automated Windows setup script (setup.ps1)
- Automated Linux/Mac setup script (setup.sh)
- One-command application launcher (run.py)
- Rich terminal output with progress tracking
- Automatic directory structure creation
- Database schema initialization
- **Testing**
- Comprehensive test suite (test_cancer_at_home.py)
- Module import tests
- Integration tests
- Directory structure validation
#### Features Highlights
βœ“ **Easy Installation**: 5-minute setup with automated scripts
βœ“ **Interactive Dashboard**: Modern web UI with real-time updates
βœ“ **Graph Visualization**: Neo4j-powered relationship mapping
βœ“ **Flexible Querying**: Both REST and GraphQL APIs
βœ“ **Distributed Computing**: BOINC integration for heavy workloads
βœ“ **Real Data**: GDC Portal integration for cancer genomics
βœ“ **Bioinformatics**: Complete FASTQ β†’ BLAST β†’ VCF pipeline
βœ“ **Well Documented**: 7 documentation files covering all aspects
βœ“ **Production Ready**: Error handling, logging, configuration
#### Technical Specifications
- **Python**: 3.8+
- **Neo4j**: 5.13 Community Edition
- **FastAPI**: 0.104.1
- **Docker**: Latest
- **Supported OS**: Windows, Linux, macOS
#### Sample Data Included
**Genes**: TP53, BRAF, BRCA1, BRCA2, PIK3CA, KRAS, EGFR
**Cancer Types**: Breast Cancer, Lung Adenocarcinoma, Colon Adenocarcinoma, Glioblastoma
**Projects**: TCGA-BRCA, TCGA-LUAD, TCGA-COAD, TCGA-GBM, TARGET-AML
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## Version Numbering
This project follows [Semantic Versioning](https://semver.org/):
- **MAJOR**: Incompatible API changes
- **MINOR**: New functionality, backwards compatible
- **PATCH**: Bug fixes, backwards compatible
---
## Future Roadmap
### Planned Features (v2.1.0)
- [ ] Machine learning for mutation prediction
- [ ] Multi-omics data integration (RNA-seq, proteomics)
- [ ] Advanced graph algorithms (PageRank, community detection)
- [ ] Export and report generation (PDF, Excel)
- [ ] User authentication and authorization
- [ ] Data caching for improved performance
### Planned Features (v2.2.0)
- [ ] Survival analysis and clinical outcomes
- [ ] Drug response prediction
- [ ] Mobile-responsive design improvements
- [ ] Real-time collaboration features
- [ ] Batch data import wizard
- [ ] Advanced search and filtering
### Long-term Goals
- [ ] Cloud deployment support (AWS, Azure, GCP)
- [ ] Kubernetes orchestration
- [ ] Microservices architecture
- [ ] Real-time BOINC cluster management
- [ ] Integration with additional data sources
- [ ] AI-powered data analysis
---
## Contributing
Contributions are welcome! Please see CONTRIBUTING.md (to be created) for guidelines.
---
## Support
For issues, questions, or suggestions:
- Check the documentation first
- Review logs in `logs/cancer_at_home.log`
- Open a GitHub issue (if applicable)
---
## Acknowledgments
Built with inspiration from:
- Cancer@Home v1 (HeroX DCx Challenge)
- Andrew Kamal's Neo4j Cancer Visualization Dashboard
- The Cancer Genome Atlas (TCGA) Project
- BOINC Project at UC Berkeley
Data provided by:
- Genomic Data Commons (GDC) Portal
- National Cancer Institute (NCI)
- The Cancer Genome Atlas Program
---
**Cancer@Home v2** - Making cancer genomics research accessible, distributed, and visual.