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FHIR UC1: ResearchStudies representation in rare disease (CMGs & Kids First) #16

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cottonva opened this issue Sep 7, 2021 · 0 comments
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@cottonva
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cottonva commented Sep 7, 2021

Platforms involved: AnVIL & Kids First
Scientific lead(s): TBD
Platform leaders: Robert Carroll & Meen Chul Kim
Datasets: Centers for Mendelian Genomics (CMGs, which specific studies), Kids First (which specific studies?)
One pager description: (what research question to be answered, plan of data use and analysis) - in development.
Use Case: Propose best practices for structuring study-level information in FHIR from rare disease studies. Incorporate into NCPI FHIR Implementation Guide https://github.com/NIH-NCPI/ncpi-fhir-ig
Funding resources: AnVIL parent funding, ODSS supplement to Kids First DRC

@cottonva cottonva changed the title FHIR: ResearchStudies representation in rare disease (CMGs & Kids First) FHIR UC: ResearchStudies representation in rare disease (CMGs & Kids First) Sep 7, 2021
@linikujp linikujp changed the title FHIR UC: ResearchStudies representation in rare disease (CMGs & Kids First) FHIR UC1: ResearchStudies representation in rare disease (CMGs & Kids First) Sep 7, 2021
@jackDiGi jackDiGi added the FHIR FHIR use case label Nov 16, 2021
@NoopDog NoopDog moved this to Needs One Pager in NCPI Use Case Tracker Dec 3, 2021
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Status: Needs One Pager
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