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Curating the Clinical Genome

Wellcome Genome Campus Wellcome Genome Campus, Hinxton, Cambridge, United Kingdom

The conference brings together the clinical genomics and biodata community to discuss best practices for the clinical use of genomic data, including interpretation and clinical utility, and the consensus generation of curated knowledge. The sharing of genetic data from clinical diagnostic testing and the generation of consensus curated knowledge is vital for delivering on the […]

Data in healthcare and life sciences – collection, innovation and data use

Online , United Kingdom

Join the Westminster Health Forum's online conference on Data in healthcare and life sciences - collection, innovation and data use.   The agenda will cover: The role of Life Sciences and data in improving patient care and outcomes - progress made since the industrial strategy and maximising impact into the future Improving the collection and […]

Antimicrobial Resistance – Genomes, Big Data and Emerging Technologies Virtual Conference

Online , United Kingdom

This year the conference will highlight the role of genomic evidence – from internal and external environments as well as its role in the detection, tracking and control of antimicrobial resistance, especially in low- and middle-income countries. Topics will include:         Global burden of disease from drug-resistant infections: monitoring and evaluation   […]

The Festival of Genomics & Biodata

Online , United Kingdom

Join the the UK’s largest genomics and biodata event this year online. The Festival spans everything from sample collection and preparation, through sequencing and genomic data analysis, to the integration of phenotypic and other biodata to make meaningful research and clinical decisions. The ultimate focus of the Festival is to deliver the benefits of genomics […]

Personal Genomes (Virtual Conference)

Online , United Kingdom

Promoting greater diversity and ethical sharing of genome data   This Wellcome Genome Campus UK virtual conference will bring together geneticists, bioinformaticians, and clinicians from academic and the commercial sector interested in learning the extent to which current genetic testing technologies can help people learn about their personal health and heritage. The meeting aims to […]

NDRS Lynch Syndrome Webinar

Online , United Kingdom

  To mark Bowel Cancer Awareness month this April, the National Disease Registration Service (NDRS) has organised a webinar to showcase the first ever national Lynch syndrome database created and how it can be used.   Lynch syndrome is a genetic condition that increases the lifetime risk of bowel cancer to up to 80%. Funded […]

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.