Notice
- Important: This guidance is under active development by NHS England and content may be added or updated on a regular basis.
- This Implementation Guide is currently in Draft and SHOULD NOT be used for development or active implementation without express direction from the NHS England Genomics Unit.
WGS Test Request - Rare Disease
For each individual WGS Test Request ordered (includes duos/trios/larger family groups), an accompanying Record of Discussion (RoD) is a mandatory requirement to progress with the test request. NGIS requires both the completion of the test request, associated sample, and the RoD, which is first routed to the appropriate Home GLH. Currently, WGS Test Requests are manually transcribed onto an electronic form within NGIS by the GLH. Rollout of direct clinician access to NGIS remains limited.
In the future state, the electronic test request, sample, and RoD (electronic or pdf attachment) will be completed by members of the requesting team. Information may be completed at different stages and the GLH may receive the WGS test request, the sample, and the RoD at different times. The requirement is to remove the double entry of the test order and RoD into NGIS and provide the GLH with the ability to forward on all order components electronically to NGIS. The central service will indicate when each component (Test order, sample, and RoD) has been received by the GLH and once all components have been forwarded onto to GEL.
Representation of the RoD form can be through either an uploaded PDF or an electronically filled form. These SHOULD be linked through the Consent.source element. The Source element MAY either be a pointer to the location of the PDF version of the RoD, either hosted by the source/client system, accessed via NRL; or embedded within the message payload, base64 encoded (using sourceAttachment); or a reference to a QuestionnaireResponse resource (using sourceReference), if this has been collected in a structured format, using the Questionnaire-Genomic Testing RoD template.
For further details on WGS Test Requesting and RoD, refer to WGS Resources and Genomics England.
NOTE: For WGS Tumour First - Germline Late scenarios, it is expected that each would be send as in individual request (ServiceRequest), linking the 2 via basedOn, i.e. the Germline ServiceRequest would reference the Tumour ServiceRequest, via ServiceRequest.basedOn. Each ServiceRequest would reference the relevant specimen, tumour or germline.
The following steps is a walk through of a WGS Test order workflow:
Link to the High Fidelity Wireframe for the WGS Rare Disease Test Scenario
1. Requester searching for a patient (a dummy patient has been pre-populated as an example) - Via PDS GET /Patient request
Parameters:
given=Lindsay
family=Sorrell
birthdate=eq2011-04-12
Response:
Patient-LindsaySorrellPDS-Example