South East Genomics

CONTACT US

Get in touch if you have any questions about the South East GLH and the tests provided. You can complete the online form below or email us.

Please note that we are no longer recruiting participants for the 100,000 Genomes Project. If you are a current participant and wish to find out about your progress in the 100,000 Genomes Project, please contact the Project Team via email or call 020 7188 8138.

Online form

Help us direct your message to the most appropriate expert by completing all fields in the form below. We will respond to all queries as soon as possible.

This contact form is not for hospital appointments and queries regarding your hospital care. If you need to cancel or rearrange an appointment, please contact the clinical team at your hospital. Any queries about results that are not from the 100,000 Genomes Project will also need to be directed to your clinical team.

We will only use your email address to contact you regarding your query. Your email address will be deleted after your query has been answered.

 

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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.