This page is part of the FHIR Specification (v4.3.0-snapshot1: Release 4B Snapshot #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 |
Raw JSON (canonical form + also see JSON Format Specification)
MolecularSequence example from precisionFDA
{ "resourceType": "MolecularSequence", "id": "fda-example", "text": { "status": "generated", "div": "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p><b>Generated Narrative</b></p><div><p>Resource "fda-example" </p></div><p><b>type</b>: dna</p><p><b>coordinateSystem</b>: 1</p><p><b>patient</b>: <a>Patient/example</a> "Peter CHALMERS"</p><h3>ReferenceSeqs</h3><table><tr><td>-</td><td><b>ReferenceSeqId</b></td><td><b>Strand</b></td><td><b>WindowStart</b></td><td><b>WindowEnd</b></td></tr><tr><td>*</td><td>NC_000001.11 <span> (nuccore#NC_000001.11)</span></td><td>watson</td><td>10453</td><td>101770080</td></tr></table><h3>Variants</h3><table><tr><td>-</td><td><b>Start</b></td><td><b>End</b></td><td><b>ObservedAllele</b></td><td><b>ReferenceAllele</b></td></tr><tr><td>*</td><td>13116</td><td>13117</td><td>T</td><td>G</td></tr></table><h3>Qualities</h3><table><tr><td>-</td><td><b>Type</b></td><td><b>StandardSequence</b></td><td><b>Start</b></td><td><b>End</b></td><td><b>Method</b></td><td><b>TruthTP</b></td><td><b>QueryTP</b></td><td><b>TruthFN</b></td><td><b>QueryFP</b></td><td><b>GtFP</b></td><td><b>Precision</b></td><td><b>Recall</b></td><td><b>FScore</b></td></tr><tr><td>*</td><td>snp</td><td>file-Bk50V4Q0qVb65P0v2VPbfYPZ <span> (#file-Bk50V4Q0qVb65P0v2VPbfYPZ)</span></td><td>10453</td><td>101770080</td><td>Vcfeval + Hap.py Comparison <span> (#job-ByxYPx809jFVy21KJG74Jg3Y)</span></td><td>7749</td><td>7984</td><td>2554</td><td>10670</td><td>2186</td><td>0.428005</td><td>0.752111</td><td>0.545551</td></tr></table><h3>Repositories</h3><table><tr><td>-</td><td><b>Type</b></td><td><b>Url</b></td><td><b>Name</b></td><td><b>VariantsetId</b></td></tr><tr><td>*</td><td>login</td><td><a>https://precision.fda.gov/files/file-Bx37ZK009P4bX5g3qjkFZV38</a></td><td>FDA</td><td>file-Bx37ZK009P4bX5g3qjkFZV38</td></tr></table></div>" }, "type": "dna", "coordinateSystem": 1, "patient": { "reference": "Patient/example" }, "referenceSeq": { "referenceSeqId": { "coding": [ { "system": "http://www.ncbi.nlm.nih.gov/nuccore", "code": "NC_000001.11" } ] }, "strand": "watson", "windowStart": 10453, "windowEnd": 101770080 }, "variant": [ { "start": 13116, "end": 13117, "observedAllele": "T", "referenceAllele": "G" } ], "quality": [ { "type": "snp", "standardSequence": { "coding": [ { "system": "https://precision.fda.gov/files/", "code": "file-Bk50V4Q0qVb65P0v2VPbfYPZ" } ] }, "start": 10453, "end": 101770080, "method": { "coding": [ { "system": "https://precision.fda.gov/jobs/", "code": "job-ByxYPx809jFVy21KJG74Jg3Y" } ], "text": "Vcfeval + Hap.py Comparison" }, "truthTP": 7749, "queryTP": 7984, "truthFN": 2554, "queryFP": 10670, "gtFP": 2186, "precision": 0.428005, "recall": 0.752111, "fScore": 0.545551 } ], "repository": [ { "type": "login", "url": "https://precision.fda.gov/files/file-Bx37ZK009P4bX5g3qjkFZV38", "name": "FDA", "variantsetId": "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.