kemal
5463f489a3
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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.
8 lines
203 B
Docker
8 lines
203 B
Docker
FROM python:3.12-slim
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WORKDIR /ml
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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 rarelens_ml ./rarelens_ml
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ENTRYPOINT ["python", "-m", "rarelens_ml.train"]
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