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End-to-end variant interpretation platform for rare genetic disease research: SvelteKit UI, FastAPI + PostgreSQL API, Nextflow/Ensembl VEP pipeline, LightGBM pathogenicity scoring with MLflow, K8s/ArgoCD/GCP infrastructure. Public test data only; no clinical claims.
9 lines
216 B
Docker
9 lines
216 B
Docker
FROM python:3.12-slim
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WORKDIR /app
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RUN pip install --no-cache-dir uv
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COPY pyproject.toml .
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RUN uv pip install --system -e .
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COPY . .
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EXPOSE 8000
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CMD ["uvicorn", "app.main:app", "--host", "0.0.0.0", "--port", "8000"]
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