South East Genomics

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Find out more about recent genomic developments in our region or nationally. You can stay regularly updated with South East Genomics by signing up to receive our newsletter or follow us on Twitter.

A different kind of PPE #FoG2021

A different kind of PPE #FoG2021 There were many important and thought-provoking topics discussed at this year’s Festival of Genomics ...

Pathology Spotlight – Q&A with Dr Marc Ooft

PATHOLOGY SPOTLIGHT ……………………………… To mark National Pathology week, we spoke with Dr Marc Ooft, Consultant Histopathologist at King’s College Hospital, ...

Kati Paalosalo-Harris Frontline- NEWS

Cancer risk assessment and genetics

Cancer risk assessment and genetics Specialist family history nurse, Kati Paalosalo-Harris, on cancer risk levels in families and common misconceptions ...

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South East Genomics

Welcome to our new home

We have recently changed our name from the NHS London South Genomic Laboratory Hub to the NHS South East Genomic Laboratory Hub. We think it better reflects the region we cover!

Read the full announcement here
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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.