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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.
13 lines
331 B
Python
13 lines
331 B
Python
import pytest
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from httpx import ASGITransport, AsyncClient
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from app.main import app
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@pytest.mark.asyncio
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async def test_health():
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async with AsyncClient(transport=ASGITransport(app=app), base_url="http://test") as c:
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r = await c.get("/health")
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assert r.status_code == 200
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assert r.json() == {"status": "ok"}
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