Initial release: rarelens platform skeleton (AGPL-3.0)

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.

pipeline/Dockerfile

@@ -0,0 +1,5 @@
+# Loader image: pandas + psycopg for LOAD_DB
+FROM python:3.12-slim
+RUN pip install --no-cache-dir pandas sqlalchemy "psycopg[binary]"
+COPY bin/load_db.py /usr/local/bin/load_db.py
+RUN chmod +x /usr/local/bin/load_db.py