Initial release: rarelens platform skeleton (AGPL-3.0)
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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.
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2026-09-11 16:55:35 +01:00
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FROM python:3.12-slim
WORKDIR /ml
RUN pip install --no-cache-dir uv
COPY pyproject.toml .
RUN uv pip install --system -e .
COPY rarelens_ml ./rarelens_ml
ENTRYPOINT ["python", "-m", "rarelens_ml.train"]