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Difference between revisions of "201601 FHIR Genomics"
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==Justification== | ==Justification== | ||
| + | The Sequence resource is a core resource in FHIR Genomics. It is used to represent complex genetics data. | ||
<!--Why is this an important track to include in the connectathon - include implementer need, impact on ballot, FMM readiness of the resources, etc. --> | <!--Why is this an important track to include in the connectathon - include implementer need, impact on ballot, FMM readiness of the resources, etc. --> | ||
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==Proposed Track Lead== | ==Proposed Track Lead== | ||
Revision as of 17:32, 11 November 2015
Contents
Sequence resource
Submitting WG/Project/Implementer Group
Justification
The Sequence resource is a core resource in FHIR Genomics. It is used to represent complex genetics data.
Proposed Track Lead
Gil Alterovitz
Expected participants
The number of the participants may be 20-50.
Roles
FHIR Client
Support the sending of the Sequence resource operations: create, history, read, search and update.
FHIR Server
Support the receiving and processing of the Patient resource operations: create, history, read, search and update.
Steps
Scenario Step 1 Register a new sequence
- Action: FHIR Client. Create a sequence instance to represent genetics data (DNA variant, RNA sequence, structural variant, etc).
- Precondition: This sequence instance does not exist in service prior to action.
- Success Criteria: Sequence created correctly on server and in the desired format.
- Bonus point:
Example for genetics data representation:
