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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 referral. These include obtaining a family history, identify high risk family histories, approaches to genetic testing, consent taking and counselling skills associated with providing information […]

Equality, Diversity and Inclusion (EDI) for Genomic Professionals

Equality, Diversity and Inclusion (EDI) for Genomic Professionals 9 – 10 January 2023 | Online course Guy’s and St Thomas’ Equality, Diversity and Inclusion (EDI) for Genomic Professionals Course will highlight the fundamental approaches and limitations for professionals keen to ensure equality, diversity and inclusion in their genomic practice. Through the use of action learning […]

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 […]

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, learn and celebrate! This year's Festival will bring you inspirational speakers, the latest research and clinical breakthroughs, cutting-edge technology and incredible networking opportunities. The Festival […]

Lunch & Learn – Renal Genomics: Steroid-Resistant Nephrotic Syndrome

via Microsoft Teams , United Kingdom

Bio's: Ania Koziell-An introduction to Genomic SRNS, Ania is a consultant nephrologist and Senior Lecturer with a research focus on the genomics of kidney disease. She is also the lead for Renal Genomics for the South East Genomic Medicine Alliance (GMSA) which aims to implement genomics into the NHS to support a precision medicine approach thus […]

Rare Disease Day on 28th February 2023 #showyourstripes

M4RD is busy getting ready for Rare Disease Day on 28th February. We’re asking people to “show their stripes” in support of the rare disease community by wearing a pair of stripy socks on the day, taking a photo and posting it online.

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 of a genomics test result for family members. This event is free and open to all, click here to secure your spot. The recording from […]

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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.