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/modules/load_db.nf

@@ -0,0 +1,13 @@
+process LOAD_DB {
+    tag "$job_id"
+    input:
+        path tsv
+        val job_id
+        val db_url
+    output: stdout
+
+    script:
+    """
+    load_db.py --tsv $tsv --job-id $job_id --db-url '$db_url'
+    """
+}