This page is part of the FHIR Specification (v3.3.0: R4 Ballot 2). 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 | Ballot Status: Informative | Compartments: Not linked to any defined compartments |
This is the narrative for the resource. See also the XML or JSON format. This example conforms to the profile Sequence.
Generated Narrative with Details
id: fda-vcf-comparison
coordinateSystem: 1
patient: Patient/example
- | ReferenceSeqId | Strand | WindowStart | WindowEnd |
* | NC_000001.11 (Details : {http://www.ncbi.nlm.nih.gov/nuccore code 'NC_000001.11' = 'NC_000001.11) | watson | 10453 | 101770080 |
- | Start | End | ObservedAllele | ReferenceAllele |
* | 13116 | 13117 | T | G |
- | Type | StandardSequence | Start | End | Score | Method | TruthTP | TruthFN | QueryFP | GtFP | Precision | FScore |
* | unknown | file-BkZxBZ00bpJVk2q6x43b1YBx (Details : {https://precision.fda.gov/files/ code 'file-BkZxBZ00bpJVk2q6x43b1YBx' = 'file-BkZxBZ00bpJVk2q6x43b1YBx) | 10453 | 101770080 | 5.000 | VCF Comparison (Details : {https://precision.fda.gov/apps/ code 'app-BqB9XZ8006ZZ2g5KzGXP3fpq' = 'app-BqB9XZ8006ZZ2g5KzGXP3fpq) | 129481 | 3168 | 1507 | 2186 | 0.9885 | 0.9823 |
- | Type | Url | Name |
* | login | https://precision.fda.gov/comparisons/1850 | 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.