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.
6 lines
219 B
Docker
6 lines
219 B
Docker
# Loader image: pandas + psycopg for LOAD_DB
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FROM python:3.12-slim
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RUN pip install --no-cache-dir pandas sqlalchemy "psycopg[binary]"
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COPY bin/load_db.py /usr/local/bin/load_db.py
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RUN chmod +x /usr/local/bin/load_db.py
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