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Type:
Change Request
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Resolution: Persuasive with Modification
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Priority:
Medium
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Genomics Reporting (FHIR)
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STU3
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Clinical Genomics
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(profiles) [deprecated]
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1.2.6
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Bob M / Clem : 19-0-0
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Correction
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Compatible, substantive
Existing Wording: The?Sequenced Variants?section deals with all types of variants detected by formal sequencing, including simple/discrete variants, structural variants and complex variants detected by direct sequencing, shot-gun-based sequencing and array-based testing for specific variants.
Proposed Wording: The?Sequence Variants?section deals with all types of variants detected by formal sequencing, including simple/discrete variants, structural variants and complex variants detected by direct sequencing, shot-gun-based sequencing and array-based testing for specific variants.
Comment:
Think the name "sequenced' is is not right. Think report would also deliver results from a package of probes and array based testing is not a sequencing method. I think variants reported or observed variants would be better. Assume you are trying to distinguish it from legacy Cytogenetics which was excluded in the original plan and will be
Summary:
Consider variants reported or observed variants in lieu of Sequenced Variants
- is voted on by
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BALLOT-5514 Negative - Clement McDonald : 2018-May-FHIR IG CG R1
- Balloted