Rare Disease Genomics
GenomeDx ultraRapid — Inpatient Genome Sequencing
AC-GDX-TH78B · GeneDx
Accelerated genome sequencing for critically ill infants and children in the NICU or PICU, where a molecular diagnosis may change management within the admission. Requires coordination before collection — do not order this pathway without confirming the timeline with AC first.
Order this test
Send the clinical question and specimen details and AC confirms the pathway, collection requirements, and logistics.
Order in the portalNot a client yet? Ask usHow ordering works →Test details
- Test code
- AC-GDX-TH78B
- Performing lab
- GeneDx
- Clinical area
- Rare Disease Genomics
- Method
- Rapid or ultra-rapid whole genome sequencing — duo or trio
- Specimen
- EDTA whole blood
- Turnaround
- ~18 days incl. shipping
Turnaround is quoted end to end — the reference laboratory’s processing time plus courier transit from Jordan, 5 days to Korea and 8 days to the United States. It is indicative, not a guarantee, and may vary with specimen quality and shipment timing.
Sample requirements
Collect EDTA whole blood. Full handling, storage, and stability requirements are confirmed when you order. See sample requirements for general collection guidance.
Other tests in Rare Disease Genomics
For healthcare professionals. Tests are ordered and interpreted in consultation with a qualified physician. Test names are the performing laboratory’s own. Pricing is per-institution and confirmed on request.