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Science Policy: Improving the Uptake of Research into UK Policy Virtual Conference

Online , United Kingdom

This event will provide early career researchers (PhD students, post-doctoral fellows and early career faculty) with an introduction to policymaking, show them how to engage with policy makers, either by their research being used to influence policy or by moving into a career in science policy. Topics will include: How does research inform policy? Getting […]

Westminster Health Forum: Next steps for rare diseases and specialised commissioning

Online , United Kingdom

Next steps for rare diseases and specialised commissioning - policy priorities, utilising genomics, patient engagement and co-ordinating care   This online conference orgainsed by the Westminster Health Forum will discuss the key policy priorities and next steps for improving outcomes in rare diseases and specialised commissioning in England. Key areas for discussion: the UK Strategy […]

Recurring

Wellcome Trust Nursing Genomics & Healthcare Virtual Conference

Online , United Kingdom

Nurses comprise over 50% of the global healthcare workforce, and have an important role in bringing the benefits of genomics to patients. Despite this, genomics has not been systematically incorporated into nursing teaching curricula, and there have been no significant changes in nursing practice that bring genomics into day-to-day health care. The inaugural conference aims to […]

Westminster Health Forum: Priorities for rare disease research, diagnosis, and care in the UK

Online , United Kingdom

This online Westminster Health Forum conference will discuss the next steps for rare diseases policy in the UK. Delegates will assess: the Rare Diseases Framework -  priorities going forward if its ambitions are to be delivered, as well as progress during it first year the impact of the pandemic the role of genomics in improving diagnosis […]

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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.