education

Congenica EGM2020- Genomic Medicine

Enabling Genomic Medicine 2020: Mainstreaming Genomics

Join global genomics experts at the forefront of precision medicine for this free virtual event presenting the latest innovations and best practices for mainstreaming genomics to enable routine clinical care, diagnosis, and treatment.   Speakers include: Prof. Sanjay Sisodiya Director of Genomics & Professor of Neurology, UCL Dr. Michael Phillips Chief Scientific Officer, Sequence Bio …

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SGUL Postgraduate Virtual Open Evening- Event

SGUL Postgraduate Virtual Open Evening

Join the St George’s Postgraduate Virtual Open Evening on Thursday 6th August, where you can hear about the available postgraduate courses, including the Genomics MSc, and speak with course directors from the comfort of your home.   For more details and to register, visit the St George’s event page.

Cancer Genetics Course 2020

Cancer Genetics Course 2020

What is Guy’s Cancer Genetics course? This 4-day course covers a breadth of topics pertinent to the rapidly moving field of genomics, impacting all areas of healthcare. We will equip you with the basics of cancer genetic counselling, approaches to genetic testing, management of hereditary cancers and a consent taking workshop, covering a variety of …

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Curating the Clinical Genome Conference

Curating the Clinical Genome

The conference brings together the clinical genomics and biodata community to discuss best practices for the clinical use of genomic data, including interpretation and clinical utility, and the consensus generation of curated knowledge. The sharing of genetic data from clinical diagnostic testing and the generation of consensus curated knowledge is vital for delivering on the …

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Genomic Variant Interpretation Course

Genomic Variant Interpretation Course

The University of Manchester (UoM) have launched a new continuing professional development (CPD) course, funded by the HEE, which provides an introduction to the tools and procedures used in the interpretation of genetic variants in the clinical setting. This free course is aimed at Consultant Clinical geneticists, Genetic Counsellors (who have not undertaken STP training), …

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Genomic Variant Interpretation Course

Genomic Variant Interpretation Course

The University of Manchester (UoM) have launched a new continuing professional development (CPD) course, funded by the HEE, which provides an introduction to the tools and procedures used in the interpretation of genetic variants in the clinical setting. This free course is aimed at Consultant Clinical geneticists, Genetic Counsellors (who have not undertaken STP training), …

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Familial Hypercholesterolaemia Symposium 2020 event

Live stream: Familial Hypercholesterolaemia Symposium 2020

  The Royal Society of Medicine is dedicating an entire day to the in-depth understanding of genetic causes, identification and management of Familial Hypercholesterolaemia (FH). From this live streamed event, you will have an unprecedented opportunity to learn about this under-diagnosed, potentially fatal, but eminently treatable disorder. View the full agenda and register on the …

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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 HubWe think it better reflects the region we cover!

Hello! Welcome to the South East GLH website. The site is not fully supported in older versions of Internet Explorer. To get the best experience, we recommend that you use Google Chrome or Firefox to browse the site.

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.