South East Genomics

South East Genomics

Search
Close this search box.

QGenome for prenatal is here!

Leave a Comment / News / By

 

We are delighted to announce that our QGenome tool has expanded to offer information and guidance to NHS staff working within prenatal.

QGenome is a free online tool that offers clinicians readily-accessible, evidence-based clinical guidance and a streamlined mechanism to instigate genomic investigations and onward referrals, where necessary. It is freely available on iOS, Android and Web apps.

Get more information about QGenome here

QGenome now available for prenatal professionals
QGenome now available for prenatal professionals

 

Leave a Comment

Your email address will not be published. Required fields are marked *

About Us

GMS Alliance

Genomic Laboratory Hub

Patients and Public

Educational Resources

News and Events

© South East Genomics 2020

Privacy and Terms

Twitter
Contact us
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.