Professional

  • Overview
  • How to order a test
  • National test directory
  • Getting the results
  • 100k guidance for clinicians
  • Educational resources
  • Education & Training events calendar

Genomic medicine is now part of mainstream NHS care and all healthcare professionals (not just genetics specialists) need to have a good understanding of its relevance. The pathway below outlines the Whole Genome Sequencing (WGS) pathway. 

STEP 1
Clinician requests a test from the National Test Directory by completing a Test Order Form and sending this to the GLH with the Patient Choice form and appropriate samples.
STEP 2
The GLH receive the forms and samples. The information from these forms are entered into the NGIS Test Ordering System. DNA is extracted from the samples.
STEP 3
THe GLH sends all required DNA samples for WGS testing to the plating organisation.
STEP 4
The GLH performs interpretation and issues a NHS Genomic Report to the ordering clinician.
Resource library- Professionals

Library of resources

Carefully created and curated for healthcare professionals across the region to make the best use of genomics in their practice.

Calendar- Professionals

Education & events calendar

Our programme of genomics education for healthcare professionals is delivered through a mixture of face-to-face and online events.

We want to hear from you!

How to order a test

Cancer
test order form

Rare disease
test order form

Record of Discussion form

National test directory

The National Genomic Test Direcctory

The 2020/2021 National Genomic Test Directory specifies which genomic tests are commissioned by the NHS in England, the technology by which they are available, and the patients who will be eligible to access to a test. 

Getting results

All genetic and genomic test results will be returned by the London South Genomic Laboratory Hub after appropriate interpretation and analysis has been completed. These reports will be returned directly to the ordering clinician, unless instructed otherwise.

A GTAB meeting at Guy's Hospital- Clinicians
A GTAB meeting at Guy’s Hospital- Clinicians

Results will need to be discussed at a Genomic Tumour Advisory Board meeting prior to a report being issued. These meetings have been established to ensure there is appropriate expert knowledge and oversight of genomic test results and that they are managed and acted upon in a coordinated way.  These GTAB meetings will take place on a regular basis across the London South region and responsible clinicians will be invited to their local meeting to review their patient’s results with the Board members. Below is a mapping of the overall MDT model through which genomic test results will be monitored and reviewed.

Getting results- Clinicians

A GARD meeting at Guy's Hospital- Professionals
A GARD meeting at Guy’s Hospital- Professionals

Results will need to be discussed by the Genomic Advisory team for Rare Disease at a MDT meeting prior to a report being issued. These meetings have been established to ensure there is appropriate expert knowledge and oversight of genomic test results and that they are managed and acted upon in a coordinated way.  These GARD meetings will take place on a regular basis across the London South region and responsible clinicians will be invited to their local meeting to review their patient’s results. Below is a mapping of the overall MDT model through which genomic test results will be monitored and reviewed.

Getting results- Professionals

100k guidance for clinicians

A big thank you to all the healthcare professionals in the South London, Kent, Surrey and Sussex region who helped recruit over 2000 Cancer participants and nearly 4000 Rare Disease participants and their families to the Project. Recruitment to the Project has now come to an end and our current focus is on returning the results of the project to patients. Your continued cooperation and support are critical in ensuring this happens.

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Referring clinicians may be invited to a Genomic MDT meeting to review the results and discuss next steps for the patient. Depending on this discussion, more work may be required before the final result can be returned to the referring clinician (i.e. further analysis and validation of the findings).

In some cases an MDT discussion may not be appropriate and the report may be issued directly after the analysis at the lab. The referring clinician is then responsible for discussing the result with the patient.

Information for healthcare professionals on the 100,000 Genomes Project can be found on the Genomics England website:

Education & Training events calendar

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Events for December 2020

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Calendar of Events

Calendar of Events
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Elizabeth Blackwell Annual Public Lecture 2020: Genomics and personalised medicine

Mitochondrial Medicine Virtual Conference

Mitochondrial Medicine Virtual Conference

Mitochondrial Medicine Virtual Conference

The genomic revolution: A practical guide to what you can’t afford not to know Part 1

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Glasgow Pathology 2020

Glasgow Pathology 2020

Virtual Cancer Genetics Course 20/21

Glasgow Pathology 2020

Virtual Cancer Genetics Course 20/21

Fertility, Genomics and COVID-19: PET Annual Conference

ERN GENTURIS webinar: PTEN hamartoma tumour syndrome

The genomic revolution: A practical guide to what you can’t afford not to know – Part 2

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Derivation and Culture of Human Induced Pluripotent Stem Cells (hiPSCs) Virtual Course

Derivation and Culture of Human Induced Pluripotent Stem Cells (hiPSCs) Virtual Course

Derivation and Culture of Human Induced Pluripotent Stem Cells (hiPSCs) Virtual Course

Derivation and Culture of Human Induced Pluripotent Stem Cells (hiPSCs) Virtual Course

The genomic revolution: A practical guide to what you can’t afford not to know – Part 3

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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.
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.

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