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Specification:

Genomics Reporting (FHIR)
Raised in Version:

1.0 [deprecated]
Work Group:

Clinical Genomics
Related URL:
http://build.fhir.org/ig/HL7/genomics-reporting/sequencing.html
Related Artifact(s):

Variant
Resolution Description:

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Update the content of http://build.fhir.org/ig/HL7/genomics-reporting/sequencing.html with streamlined text on intended scope of Variant and use of components informed from the IM work (preview on https://build.fhir.org/ig/HL7/genomics-reporting/branches/variant-component-groups/sequencing.html) and remove outdated section at bottom of variant page. Update examples to be consistent with this guidance.

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Update the content of http://build.fhir.org/ig/HL7/genomics-reporting/sequencing.html with streamlined text on intended scope of Variant and use of components informed from the IM work (preview on https://build.fhir.org/ig/HL7/genomics-reporting/branches/variant-component-groups/sequencing.html ) and remove outdated section at bottom of variant page. Update examples to be consistent with this guidance.
Resolution Vote:
Arthur Herman / Dan Rutz : 12 - 0 - 0
Change Category:
Clarification
Change Impact:
Non-substantive

The descriptive text below the Variant model should be updated to reflect decisions made through discussions about "IG Lite" found in this document: https://docs.google.com/document/d/15g1rngmgFoE8_i7UGpXRpISkOCrd1QCoQBg9REY80EI/edit#

This is a working document and once it's finished, it can replace/add to the text on the Variant Reporting page to guide readers.

is voted on by

BALLOT-18590 Negative - Clement McDonald : 2021-May-FHIR IG CG R1 STU