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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. -->
The Sequence resource is a core resource in FHIR Genomics. It is used to represent complex genetics data.
 
  
 
==Proposed Track Lead==
 
==Proposed Track Lead==

Revision as of 17:32, 11 November 2015

Sequence resource

Submitting WG/Project/Implementer Group

CG

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:

TestScript(s)