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.
10 lines
290 B
Terraform
10 lines
290 B
Terraform
resource "google_container_cluster" "rarelens" {
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name = "rarelens"
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location = var.region
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enable_autopilot = true
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deletion_protection = false
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workload_identity_config { workload_pool = "${var.project}.svc.id.goog" }
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release_channel { channel = "REGULAR" }
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}
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