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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resource "google_storage_bucket" "data" {
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name = "${var.project}-rarelens-data"
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location = var.region
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uniform_bucket_level_access = true
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lifecycle_rule {
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condition {
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age = 30
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matches_prefix = ["work/"]
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}
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action { type = "Delete" }
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}
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}
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resource "google_artifact_registry_repository" "images" {
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repository_id = "rarelens"
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location = var.region
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format = "DOCKER"
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}
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resource "google_pubsub_topic" "vcf_uploaded" { name = "vcf-uploaded" }
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