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--- |
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base_model: |
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- unsloth/gemma-3n-E4B-it-unsloth-bnb-4bit |
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pipeline_tag: text-generation |
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library_name: transformers |
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language: |
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- en |
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license: apache-2.0 |
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datasets: |
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- ClinVar |
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- COSMIC |
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tags: |
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- medical |
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- genomics |
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- cancer |
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- oncology |
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- mutation-analysis |
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- precision-medicine |
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- GGUF |
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- Ollama |
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model_type: gemma3n |
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quantized_by: OncoScope |
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--- |
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# OncoScope Cancer Genomics Analysis Model |
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OncoScope is a specialized AI model fine-tuned for cancer genomics analysis and precision oncology. Built on Google's Gemma 3n architecture, this model provides expert-level analysis of cancer mutations, risk assessments, and therapeutic recommendations while maintaining complete privacy through on-device inference. |
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## Model Details |
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- **Base Model**: Google Gemma 3n 2B E4B Chat IT |
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- **Parameters**: 6.9B (quantized from fine-tuned model) |
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- **Architecture**: Gemma3n |
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- **Quantization**: Q8_0 GGUF format |
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- **Context Length**: 32,768 tokens |
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- **Embedding Length**: 2,048 |
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## Key Features |
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- **Cancer Mutation Analysis**: Pathogenicity assessment using ACMG/AMP guidelines |
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- **Risk Stratification**: Hereditary cancer syndrome evaluation |
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- **Therapeutic Recommendations**: Evidence-based drug target identification |
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- **Privacy-First**: Designed for on-device inference with Ollama |
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- **Clinical Guidelines**: Incorporates established medical standards |
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- **Multi-mutation Analysis**: Complex genomic interaction assessment |
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## Training Data |
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The model was fine-tuned on a curated dataset of 5,998 cancer genomics examples from: |
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- **ClinVar**: Clinical variant database |
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- **COSMIC Top 50**: Cancer mutation signatures |
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- **Expert-curated**: Clinical oncology cases |
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## Usage |
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### With Ollama |
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1. **Download the model files**: |
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- `oncoscope-gemma-3n-merged.Q8_0.gguf` (6.8GB) |
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- `Modelfile` |
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2. **Create the model**: |
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```bash |
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ollama create oncoscope -f Modelfile |
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``` |
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3. **Run inference**: |
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```bash |
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ollama run oncoscope "Analyze the clinical significance of BRCA1 c.5266dupC mutation" |
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``` |
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### Example Usage |
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```bash |
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ollama run oncoscope "Patient: 45-year-old female with family history of breast cancer. |
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Mutation: BRCA1 c.68_69delAG (p.Glu23ValfsTer17). |
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Please provide pathogenicity assessment and recommendations." |
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``` |
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**Example Response**: |
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```json |
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{ |
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"mutation_analysis": { |
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"gene": "BRCA1", |
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"variant": "c.68_69delAG", |
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"protein_change": "p.Glu23ValfsTer17", |
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"pathogenicity": "Pathogenic", |
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"confidence_score": 0.95, |
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"acmg_classification": "PVS1, PM2, PP3" |
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}, |
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"clinical_significance": { |
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"cancer_risk": "High", |
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"associated_cancers": ["Breast", "Ovarian"], |
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"lifetime_risk": { |
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"breast_cancer": "55-85%", |
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"ovarian_cancer": "15-40%" |
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} |
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}, |
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"recommendations": { |
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"genetic_counseling": "Strongly recommended", |
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"screening": "Enhanced surveillance starting age 25", |
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"prevention": "Consider prophylactic surgery", |
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"family_testing": "Cascade testing recommended" |
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} |
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} |
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``` |
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## Model Capabilities |
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- **Pathogenicity Assessment**: ACMG/AMP guideline compliance |
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- **Risk Calculation**: Quantitative cancer risk estimates |
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- **Drug Recommendations**: FDA-approved targeted therapies |
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- **Family History Analysis**: Hereditary pattern recognition |
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- **Genetic Counseling**: Evidence-based guidance |
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- **Multi-lingual Support**: Medical terminology in multiple languages |
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## Limitations |
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- **Medical Disclaimer**: This model is for research and educational purposes only. Always consult qualified healthcare professionals for medical decisions. |
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- **Training Cutoff**: Knowledge based on training data through early 2024 |
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- **Quantization**: Some precision loss due to Q8_0 quantization |
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- **Context Window**: Limited to 4,096 tokens for optimal performance |
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## Technical Specifications |
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- **Model Size**: 6.8GB (GGUF Q8_0) |
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- **Memory Requirements**: 8GB+ RAM recommended |
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- **Hardware**: CPU inference optimized, GPU acceleration supported |
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- **Operating Systems**: Cross-platform (macOS, Linux, Windows) |
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## Performance |
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The model demonstrates expert-level performance on: |
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- Variant pathogenicity classification (>90% accuracy vs. clinical consensus) |
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- Cancer risk assessment correlation with established guidelines |
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- Therapeutic recommendation alignment with FDA approvals |
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- Response time: 20-40 seconds for complex genomic analysis |
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## Privacy & Security |
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- **On-Device Inference**: No data transmitted to external servers |
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- **HIPAA Compliance**: Suitable for clinical environments |
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- **Offline Operation**: Full functionality without internet connection |
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- **Data Security**: Patient genetic information remains local |
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## Citation |
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If you use this model in your research, please cite: |
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```bibtex |
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@misc{oncoscope2025, |
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title={OncoScope: Privacy-First Cancer Genomics Analysis with Gemma 3n}, |
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author={Sheldon Aristide}, |
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year={2025}, |
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url={https://huggingface.co/Zero21/OncoScope} |
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} |
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``` |
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## License |
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This model is released under the Apache 2.0 license, consistent with the base Gemma model licensing. |
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## Support & Contact |
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For questions, issues, or contributions: |
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- GitHub: [OncoScope Project](https://github.com/Aristide021/OncoScope) |
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- Issues: Please report bugs or feature requests via GitHub Issues |
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## Disclaimer |
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This AI model is intended for research and educational purposes only. It should not be used as a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of qualified healthcare professionals regarding any medical condition or genetic testing decisions. |