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Launching our NEW podcast!

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It’s here!! We’re excited to share our new podcast in partnership with experts from across the NHS Genomic Medicine Service.

First up is Dr Lydia Green who talks about the transformative impact a genomic diagnosis can have for children and their families.

Lydia is a Neurologist at Leeds Hospital where she is leading research into Inherited White Matter Disorders, and leads the unique Leukodystrophy Service. Find out more about Lydia’s work here. 

Take a listen to Lydia here 

We’ll be launching a new episode every week.

Motorway road sign with a roundabout on it and directions from The Past to The Road to Genome. An audio wave image runs across the roundabout image

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With any Whole Genome Sequencing (WGS) test ordered, a Record of Discussion (RoD) form will also need to be submitted. This document is to record the patient’s consent for genomic testing and their choice on taking part in research. Guidance on the patient choice conversation can be found here. 
 
This RoD form will be available for clinicians to download from this webpage. Once completed with the patient, it can be send to the lab with the corresponding test order form and sample.
Tests available to order will be listed in the National Genomic Test Directory. A test order form will soon be made available for clinicians on this webpage to download and complete. This form will include the address of the laboratory that the appropriate sample and completed form needs to be sent to.
 
Until the new Genomic Laboratory Service goes live, please continue to follow existing test order processes.
 
Later this year, the online test ordering tool for Whole Genome Sequencing will be integrated into the National Genomics Informatics System (NGIS) and clinicians will be able to search or filter to find a clinical indication, confirm eligibility criteria and start the test request process for their patient.