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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kemal

2026-09-11 16:55:35 +01:00

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api/app/services/__init__.py