If you are requesting a rapid whole genome sequencing test for an acutely unwell baby or child suspected to have a monogenic disorder, where rapid testing is required to guide immediate clinical management, please use the R14 service.
The R14 test is a Rapid Whole Genome Sequencing test for acutely unwell children with a likely monogenic disorder, where rapid testing is required to guide immediate clinical management.
We aim to deliver preliminary results via email within 2 weeks of samples arriving in the Exeter Genomics Laboratory.
How to order genomic testing for the R14 Rapid Whole Genome Sequencing test
Important documents can be found to the right-hand side of this page, but please refer to the full guidance on the dedicated R14 pages here.