This page is part of the FHIR Specification (v4.1.0: Release 4B Ballot #1). The current version which supercedes this version is 5.0.0. For a full list of available versions, see the Directory of published versions . Page versions: R4B R4 R3
Clinical Genomics Work Group | Maturity Level: N/A | Standards Status: Informative | Compartments: Patient |
This is the narrative for the resource. See also the XML, JSON or Turtle format. This example conforms to the profile MolecularSequence.
Generated Narrative
coordinateSystem: 1
- | ReferenceSeqId | Strand | WindowStart | WindowEnd |
* | NC_000001.11 | watson | 10453 | 101770080 |
- | Start | End | ObservedAllele | ReferenceAllele |
* | 13116 | 13117 | T | G |
quality
type: indel
standardSequence: file-BkZxBZ00bpJVk2q6x43b1YBx
start: 10453
end: 101770080
method: Vcfeval + Hap.py Comparison
truthTP: 7749
truthFN: 2554
queryFP: 10670
gtFP: 2186
precision: 0.428005
recall: 0.752111
quality
type: snp
standardSequence: file-BkZxBZ00bpJVk2q6x43b1YBx
start: 10453
end: 101770080
method: Vcfeval + Hap.py Comparison
truthTP: 92106
truthFN: 1247
queryFP: 21744
gtFP: 493
precision: 0.808602
recall: 0.986642
- | Type | Url | Name |
* | login | https://precision.fda.gov/jobs/job-ByxYPx809jFVy21KJG74Jg3Y | FDA |
Usage note: every effort has been made to ensure that the examples are correct and useful, but they are not a normative part of the specification.