Events

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Recurring

Let’s Talk: Genomics Medicine Across a Lifetime

Online , United Kingdom

Genomic tests are already available in the NHS for use in many childhood and adult cancers, inherited disorders and rare diseases, and more tests are becoming available every year through the NHS Genomic Medicine Service. To make sure everyone for whom genomics is appropriate can access the tests that are right for them, it’s important […]

Lunch and Learn: Think Patient Care, Think Genomics

Online , United Kingdom

Session One: Cystic Fibrosis screening and diagnosis Join us for our first edition of Lunch and learn, a session for nurses and midwives focused on Cystic Fibrosis. Speakers and topics covered:   Carrier testing Cathryn Moss, Principle Genetic Counsellor, St George’s Hospital This session will offer nurses and midwives a practical guide to Cystic Fibrosis […]

RCPCH Conference 2022

We are thrilled to be returning to a face-to-face conference this year. Taking place in Liverpool from 28 to 30 June, this is a great opportunity to network with colleagues once again, hear from leading voices and catch up on the latest innovations in child health at a wide range of specialty sessions. As the […]

Facing up to the genomic gap: Tackling equality and diversity in genomics

Online Webinar , United Kingdom

About this event This webinar is part of the popular Genetics of webinar series and will discuss the challenge of equality and diversity in genomic research and clinical settings and strategies to address this.  Genomic research has traditionally been focused on Caucasian populations, which leads to inherent biases in genomic findings translated into clinical research. Underrepresentation of other populations in genomic […]

Lunch and Learn: Think Patient Care, Think Genomics

Online , United Kingdom

Session Two: Monogenic Diabetes in pregnancy Join us for our second edition of Lunch and learn, a session for nurses and midwives focused on Monogenic Diabetes.   Monogenic diabetes is a rare form of diabetes caused by a mutation in a single gene and can often be misdiagnosed as type 1 diabetes. Accurate diagnosis and […]

Recurring

Clinical Genomics Service Specification Consultation Webinar

Online , United Kingdom

NHS England are currently seeking feedback on the way clinical genomics services are delivered in England. The public consultation is open from 1 September until midnight on 30 September. Click here to view the consultation documents and access the online questionnaire to provide feedback.   Join an information webinar to find out more NHS England is […]

SE Genomics Autumn Festival

via Microsoft Teams , United Kingdom

We are keen to promote our second upcoming virtual event - SE Genomics Autumn Festival. Speakers will provide an overview of how the latest developments in genomics are impacting cancer care and share their expertise on different cancer genomics pathways and the tests available. Register now via Eventbrite and please share with your networks as […]

“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 […]

Lunch and Learn: Think Patient Care, Think Genomics

Online , United Kingdom

Session Three: Lynch Syndrome Join us for our third edition of Lunch and learn, a series of webinars for nurses and midwives to gain insight into how genomic testing is used across different areas of healthcare. Professionals will share their expertise of genomic tests available for patients through different patient pathways.   Speakers and topics […]

Whole Genome Sequencing drop-in session

Online , United Kingdom

Whole Genome Sequencing Drop In Session: Tuesday 11th October, 14:30-15:30 Are you a clinician looking to find out more about Whole Genome Sequencing (WGS)? Then this drop-in session is for you! During the session you will find out more information on this new testing, how it can be used for your patients and have the […]

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.