Events

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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 […]

The Festival of Genomics & Biodata

Business Design Centre, 52 Upper St, London, N1 0QH

The Festival of Genomics & Biodata 25 – 26 January 2023 | In-Person Event WELCOME BACK to the annual get-together for the entire genomics and biodata community, to discover, meet, […]

SE Genomics Spring Festival 2023

via Microsoft Teams , United Kingdom

We are keen to promote our third upcoming virtual event - SE Genomics Spring Festival 2023. Speakers will explain the importance of consenting for a genomics test, and the implications […]

Lunch and Learn Mental Health Services

Online , United Kingdom

  Lunch and Learn: Think Patient Care, Think Genomics Mental health services and genomic medicine: embedding genomic testing in the memory clinic Join us for our tenth edition of Lunch […]

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.