This page is part of the FHIR Specification (v1.8.0: STU 3 Draft). 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
Sequence example from precisionFDA (id = "fda-example")
<Sequence xmlns="http://hl7.org/fhir"> <id value="fda-example"/> <text><status value="generated"/><div xmlns="http://www.w3.org/1999/xhtml"><p><b>Generated Narrative with Details</b></p><p><b>id</b>: fda-example</p><p><b>type</b>: DNA</p><p><b>coordinateSystem</b>: 1</p><p><b>patient</b>: <a>Patient/example</a></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>(Details : {http://www.ncbi.nlm.nih.gov/nuccore code 'NC_000001.11' = 'NC_000001.11)</span></td><td>1</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>(Details : {https://precision.fda.gov/files/ code 'file-Bk50V4Q0qVb65P0v2VPbfYPZ' = 'file-Bk50V4Q0qV b65P0v2VPbfYPZ)</span></td><td>10453</td><td>101770080</td><td>Vcfeval + Hap.py Comparison <span>(Details : {https://precision.fda.gov/jobs/ code 'job-ByxYPx809jFVy21KJG74Jg3Y' = 'job-ByxYPx809jFVy 21KJG74Jg3Y)</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></text><type value="DNA"/> <coordinateSystem value="1"/> <patient> <reference value="Patient/example"/> </patient> <referenceSeq> <referenceSeqId> <coding> <system value="http://www.ncbi.nlm.nih.gov/nuccore"/> <code value="NC_000001.11"/> </coding> </referenceSeqId> <strand value="1"/> <windowStart value="10453"/> <windowEnd value="101770080"/> </referenceSeq> <variant> <start value="13116"/> <end value="13117"/> <observedAllele value="T"/> <referenceAllele value="G"/> </variant> <quality> <type value="SNP"/> <standardSequence> <coding> <system value="https://precision.fda.gov/files/"/> <code value="file-Bk50V4Q0qVb65P0v2VPbfYPZ"/> </coding> </standardSequence> <start value="10453"/> <end value="101770080"/> <method> <coding> <system value="https://precision.fda.gov/jobs/"/> <code value="job-ByxYPx809jFVy21KJG74Jg3Y"/> </coding> <text value="Vcfeval + Hap.py Comparison"/> </method> <truthTP value="7749"/> <queryTP value="7984"/> <truthFN value="2554"/> <queryFP value="10670"/> <gtFP value="2186"/> <precision value="0.428005"/> <recall value="0.752111"/> <fScore value="0.545551"/> </quality> <repository> <type value="login"/> <url value="https://precision.fda.gov/files/file-Bx37ZK009P4bX5g3qjkFZV38"/> <name value="FDA"/> <variantsetId value="file-Bx37ZK009P4bX5g3qjkFZV38"/> </repository> </Sequence>
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.