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.
14 lines
339 B
Terraform
14 lines
339 B
Terraform
terraform {
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required_version = ">= 1.8"
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required_providers {
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google = { source = "hashicorp/google", version = "~> 6.0" }
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random = { source = "hashicorp/random", version = "~> 3.6" }
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}
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backend "gcs" { bucket = "REPLACE-tfstate", prefix = "rarelens" }
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}
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provider "google" {
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project = var.project
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region = var.region
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}
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