Events

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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 […]

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 […]

Recurring

Virtual Prenatal Genetics Short Course 2022

Online , United Kingdom

This skills based course is designed to give midwives and other health professionals working in a prenatal testing setting tools to help them to enable patients to access appropriate onwards […]

Recurring

Virtual Prenatal Genetics Short Course 2022

Online , United Kingdom

This skills based course is designed to give midwives and other health professionals working in a prenatal testing setting tools to help them to enable patients to access appropriate onwards […]

Recurring

National pathology workshops: Lynch Syndrome

Online , United Kingdom

Lynch syndrome (LS) is an inherited condition caused by pathogenic variants in DNA genes which result in an increased risk of colorectal, endometrial, and other cancers. LS affects approximately 1 […]

Recurring

Virtual Prenatal Genetics Short Course 2022

Online , United Kingdom

This skills based course is designed to give midwives and other health professionals working in a prenatal testing setting tools to help them to enable patients to access appropriate onwards […]

Recurring

Virtual Prenatal Genetics Short Course 2022

Online , United Kingdom

This skills based course is designed to give midwives and other health professionals working in a prenatal testing setting tools to help them to enable patients to access appropriate onwards […]

Recurring

National pathology workshops: Lynch Syndrome

Online , United Kingdom

Lynch syndrome (LS) is an inherited condition caused by pathogenic variants in DNA genes which result in an increased risk of colorectal, endometrial, and other cancers. LS affects approximately 1 […]

Lunch and Learn: Think Patient Care, Think Genomics

Online , United Kingdom

Session Fifth: Spinal Muscular Atrophy Spinal muscular atrophy (SMA) is a genetic condition affecting the central nervous system, peripheral nervous system, and voluntary muscle movement (skeletal muscle). During this session […]

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.