South East Genomics

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Dr Srividhya Sankaran- Maternal Fetal Medicine and Genomics NEWS

#GenomicsConversation spotlight on… Maternal-Foetal Medicine and Genomics

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Spotlight on…Maternal-Foetal Medicine #GenomicsConversation Maternal-Foetal Medicine and Genomics This week is the national #GenomicsConversation week of action, part of a campaign launched by the Genomics Education Programme (GEP) to dispel the myths, explain the facts and outline the clinical impact of genomics. At South East we will be sharing a series of interviews with different health …

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#GenomicsConversation spotlight on… Neurodisability, Epilepsy and Genomics

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Spotlight on…Neurodisbility and Epilepsy #GenomicsConversation Neurodisbility, Epilepsy and Genomics This week is the national #GenomicsConversation week of action, part of a campaign launched by the Genomics Education Programme (GEP) to dispel the myths, explain the facts and outline the clinical impact of genomics. At South East we will be sharing a series of interviews with …

#GenomicsConversation spotlight on… Neurodisability, Epilepsy and Genomics Read More »

Dr Tony Hulse- NEWS

#GenomicsConversation spotlight on… Paediatric Endocrinology and Genomics

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Spotlight on…Endocrinology #GenomicsConversation Paediatric Endocrinology and Genomics This week is the national #GenomicsConversation week of action, part of a campaign launched by the Genomics Education Programme (GEP) to dispel the myths, explain the facts and outline the clinical impact of genomics. At South East we will be sharing a series of interviews with different health professionals …

#GenomicsConversation spotlight on… Paediatric Endocrinology and Genomics Read More »

Dr Richard Dillon- NEWS

#GenomicsConversation spotlight on… Haematology and Genomics

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Spotlight on…Haematology #GenomicsConversation Haematology and Genomics This week is the national #GenomicsConversation week of action, part of a campaign launched by the Genomics Education Programme (GEP) to dispel the myths, explain the facts and outline the clinical impact of genomics. At South East we will be sharing a series of interviews with different health professionals where …

#GenomicsConversation spotlight on… Haematology and Genomics Read More »

Beth Coad- NEWS

#GenomicsConversation spotlight on… Genetic Counselling and Genomics

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Spotlight on…Genetic Counselling #GenomicsConversation Genetic Counselling and Genomics This week is the national #GenomicsConversation week of action, part of a campaign launched by the Genomics Education Programme (GEP) to dispel the myths, explain the facts and outline the clinical impact of genomics. At South East we will be sharing a series of interviews with different health …

#GenomicsConversation spotlight on… Genetic Counselling and Genomics Read More »

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), …

Genomic Variant Interpretation Course Read More »

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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!

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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.