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
type: dna
coordinateSystem: 1
- | ReferenceSeqId | Strand | WindowStart | WindowEnd |
* | NC_000001.11 | watson | 10453 | 101770080 |
- | Start | End | ObservedAllele | ReferenceAllele |
* | 13116 | 13117 | T | G |
- | Type | StandardSequence | Start | End | Method | TruthTP | QueryTP | TruthFN | QueryFP | GtFP | Precision | Recall | FScore |
* | snp | file-Bk50V4Q0qVb65P0v2VPbfYPZ | 10453 | 101770080 | Vcfeval + Hap.py Comparison | 7749 | 7984 | 2554 | 10670 | 2186 | 0.428005 | 0.752111 | 0.545551 |
- | Type | Url | Name | VariantsetId |
* | login | https://precision.fda.gov/files/file-Bx37ZK009P4bX5g3qjkFZV38 | FDA | file-Bx37ZK009P4bX5g3qjkFZV38 |
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.