Rare Disease Genomics
GenomeDx — Genome Sequencing
AC-GDX-J774B · GeneDx
Genome sequencing covering coding and non-coding regions, used where exome has been uninformative or a structural or non-coding cause is suspected. Holds FDA Breakthrough Device designation.
Order this test
Send the clinical question and specimen details and AC confirms the pathway, collection requirements, and logistics.
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- Test code
- AC-GDX-J774B
- Performing lab
- GeneDx
- Clinical area
- Rare Disease Genomics
- Method
- Whole genome sequencing — proband, duo, or trio
- Specimen
- EDTA whole blood or buccal swab
- Turnaround
- ~38 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 or buccal swab. 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.