Lynch Syndrome & Colorectal Cancer : Learn more

Online Webinar , United Kingdom

All patients with colorectal (CRC) and endometrial cancer should now receive genetic testing according to NICE guidelines.

Come and learn how you can achieve that for your patients.

Learn about Endometrial Cancer and Lynch Syndrome

Online Webinar , United Kingdom

All patients with colorectal (CRC) and endometrial cancer should now receive genetic testing according to NICE guidelines.

Come and learn how you can achieve that for your patients.

Lunch & Learn – Unique -Supporting families with rare chromosome or gene disorders

Online Webinar , United Kingdom

Unique-Supporting families with rare chromosome or gene disorders As part of rare chromosome awareness week, we are excited to be joined by representatives from Unique, who will be discussing their role in supporting patients and professionals with pre and postnatal diagnosis of rare chromosome or gene disorders. This talk will also cover topics including implications […]

Learn about Colorectal Cancer and Lynch Syndrome

Online Webinar , United Kingdom

All patients with colorectal (CRC) and endometrial cancer should now receive genetic testing according to NICE guidelines.

Come and learn how you can achieve that for your patients.

Lunch & Learn about Lynch Syndrome and Endometrial Cancer

Online Webinar , United Kingdom

All patients with colorectal (CRC) and endometrial cancer should now receive genetic testing according to NICE guidelines.

Come and learn how you can achieve that for your patients

Lunch and Learn – Inherited Epilepsies, genomics & comprehensive care

Online Webinar , United Kingdom

Lunch and Learn: Inherited Epilepsies, genomics, and comprehensive care Epilepsy is a common neurological condition. A genetic basis for epilepsy has long been known of and advances in genetic testing has increased our ability to diagnose genetic causes of epilepsy. Join our speakers to hear about    genetic epilepsy, genetic testing and pathways available for […]

Genomics Education Programme New Webinar Series

Online Webinar , United Kingdom

  The first webinar and Q&A session in the series will be broadcast live on Tuesday 24 January at 5pm and will provide an introduction to gene-directed therapies and is presented by cellular therapeutics expert Dr James Patterson. The webinar and Q&A will cover: an introduction to gene-directed therapy modalities and strategies; the use of genetic approaches for ex […]

“Everything you want to know about genomics but are afraid to ask”

Online Webinar , United Kingdom

The NHS North Thames GLH and NHS South East GLH are delighted to organise and co-host this Bayer sponsored educational meeting and welcome healthcare professional attendees from our regional cancer clinical teams. With the aim to explore the benefits and challenges of mainstreaming genomic profiling and precision oncology pathways in the management of patients with […]

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.