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Difference between revisions of "Genetics FHIR Profile Proposal"

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<!--Put a link to the resource/datatype (or group of resources) that will be profiled here.-->
 
<!--Put a link to the resource/datatype (or group of resources) that will be profiled here.-->
* [[http://hl7-fhir.github.io/observation.html|Observation]] Observation
+
* [[http://hl7-fhir.github.io/diagnosticreport.html|Observation]] DiagnosticReport
  
 
====Constraints to be Applied====
 
====Constraints to be Applied====
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<!--Describe how the current resource will be extended.-->
 
<!--Describe how the current resource will be extended.-->
* Sequence
 
 
* AssessedCondition
 
* AssessedCondition
 
* FamilyMemberHistory
 
* FamilyMemberHistory
* DiagnosticReport
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* Analysis
  
 
===Example Scenarios===
 
===Example Scenarios===
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===Scope of coverage===
 
===Scope of coverage===
  
The Standard Genetics Profile extends the Observation resource to enable reporting of structured genetic test results by referring to Sequence resource. In addition, the genetics profile denotes condition context for genetic testing, which may influence reported variants and interpretation for large genomic testing panels and provides references to the FamilyMemberHistory resource, the DiagnosticReport resource. The Card. of the extension - variant (reference to sequence-genetics variant) in the Standard genetics profile is 0...* which makes it convenient and flexible to support genetic test results containing a list of gene mutations or variants.
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The Standard Genetics Profile extends the DiagnosticReport resource to enable reporting of structured genetic test results. It denotes condition context for genetic testing, which may influence reported variants and interpretation for large genomic testing panels and provides references to the FamilyMemberHistory resource, the Condition resource.  
  
This profile supports reporting of DNA variants at the genomic, cDNA, and protein change level. In addition, a condition context may be provided, as AssessedCondition. For large genomic tests, a condition may be used as an input into the analytic pipeline to aid in the identification of clinically relevant variants related to the test order.
+
This profile supports reporting of variants at the genomic, cDNA, and protein change level. In addition, a condition context may be provided, as AssessedCondition. For large genomic tests, a condition may be used as an input into the analytic pipeline to aid in the identification of clinically relevant variants related to the test order.
  
 
Hl7 Clinical Genomics Work Group emphasizes the importance of transmitting structured genetic findings within the clinical, translational, and research environments fully integrated with other clinical data, in order to drive outcomes analysis, operational decision making, discovery research, and public health reporting.
 
Hl7 Clinical Genomics Work Group emphasizes the importance of transmitting structured genetic findings within the clinical, translational, and research environments fully integrated with other clinical data, in order to drive outcomes analysis, operational decision making, discovery research, and public health reporting.

Revision as of 03:46, 16 October 2015



Standard Genetics Profile

Profile balloting plans

Profile Details

Profiled Resource(s)

  • [[1]] DiagnosticReport

Constraints to be Applied

None

Extensions to be Applied

  • AssessedCondition
  • FamilyMemberHistory
  • Analysis

Example Scenarios

  • Genetics Test Result Reporting
  • Public Health Reporting
  • Clinical and Research Data Warehouses
  • Genetics Results with Family History
  • Gene Analysis Panel


Scope of coverage

The Standard Genetics Profile extends the DiagnosticReport resource to enable reporting of structured genetic test results. It denotes condition context for genetic testing, which may influence reported variants and interpretation for large genomic testing panels and provides references to the FamilyMemberHistory resource, the Condition resource.

This profile supports reporting of variants at the genomic, cDNA, and protein change level. In addition, a condition context may be provided, as AssessedCondition. For large genomic tests, a condition may be used as an input into the analytic pipeline to aid in the identification of clinically relevant variants related to the test order.

Hl7 Clinical Genomics Work Group emphasizes the importance of transmitting structured genetic findings within the clinical, translational, and research environments fully integrated with other clinical data, in order to drive outcomes analysis, operational decision making, discovery research, and public health reporting.


Ownership

Owning committee name

CG

Contributing or Reviewing Work Groups

Expected implementations

gForge Users

FHIR Profile Development Project Insight ID

Plans

Timelines

  • TargetDateForInternalReview

Balloting Requirements

Choose one:

  • Ballot with next FHIR DSTU or Normative Edition
  • or Ballot independently as DSTU
  • or Realm specific ballot
  • or No Ballot

Desired Ballot Date

  • PutDesiredBallotDateHere