This page is part of the Genetic Reporting Implementation Guide (v3.0.0-ballot: STU 3 Ballot 1) based on FHIR (HL7® FHIR® Standard) R4. The current version which supersedes this version is 2.0.0. For a full list of available versions, see the Directory of published versions
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<id value="analysisTumorRNA"/>
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<div xmlns="http://www.w3.org/1999/xhtml"><p><b>Generated Narrative: Procedure</b><a name="analysisTumorRNA"> </a></p><div style="display: inline-block; background-color: #d9e0e7; padding: 6px; margin: 4px; border: 1px solid #8da1b4; border-radius: 5px; line-height: 60%"><p style="margin-bottom: 0px">Resource Procedure "analysisTumorRNA" </p><p style="margin-bottom: 0px">Profile: <a href="StructureDefinition-genomic-study-analysis.html">Genomic Study Analysis</a></p></div><blockquote><p><b>Genomic Study Analysis Regions</b></p><blockquote><p><b>url</b></p><code>studied</code></blockquote><p><b>value</b>: <a href="DocumentReference-FullGenome-GRCh38.html">DocumentReference/FullGenome-GRCh38</a></p></blockquote><p><b>Genomic Study Analysis Method Type</b>: RNA analysis <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> (<a href="CodeSystem-genomic-study-method-type-cs.html">Genomic Study Method Type CodeSystem</a>#rna-analysis)</span></p><p><b>Genomic Study Analysis Change Type</b>: gene_fusion <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> (sequenceontology.org#SO:0001565)</span></p><p><b>Genomic Study Analysis Change Type</b>: transcript_variant <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> (sequenceontology.org#SO:0001576)</span></p><p><b>Genomic Study Analysis Specimen</b>: <a href="Specimen-tumorSpecimen.html">Specimen/tumorSpecimen</a></p><p><b>Genomic Study Analysis Focus</b>: <a href="Patient-somaticPatient.html">Patient/somaticPatient</a> " HAMSBURG"</p><p><b>status</b>: completed</p><p><b>category</b>: Laboratory <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> (<a href="http://terminology.hl7.org/5.3.0/CodeSystem-observation-category.html">Observation Category Codes</a>#laboratory)</span></p><p><b>subject</b>: <a href="Patient-somaticPatient.html">Patient/somaticPatient</a> " HAMSBURG"</p><p><b>performed</b>: 2023-02-02 01:01:10-0600</p></div>
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<extension url="studied">
<valueReference>🔗
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<code value="rna-analysis"/>
<display value="RNA analysis"/>
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<extension
url="http://hl7.org/fhir/uv/genomics-reporting/StructureDefinition/genomic-study-analysis-change-type">
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<coding>
<system value="http://sequenceontology.org"/>
<code value="SO:0001565"/>
<display value="gene_fusion"/>
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<extension
url="http://hl7.org/fhir/uv/genomics-reporting/StructureDefinition/genomic-study-analysis-change-type">
<valueCodeableConcept>
<coding>
<system value="http://sequenceontology.org"/>
<code value="SO:0001576"/>
<display value="transcript_variant"/>
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<extension
url="http://hl7.org/fhir/uv/genomics-reporting/StructureDefinition/genomic-study-analysis-specimen">
<valueReference>🔗
<reference value="Specimen/tumorSpecimen"/>
</valueReference>
</extension>
<extension
url="http://hl7.org/fhir/uv/genomics-reporting/StructureDefinition/genomic-study-analysis-focus">
<valueReference>🔗
<reference value="Patient/somaticPatient"/>
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<status value="completed"/>
<category>
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<system
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<code value="laboratory"/>
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<subject>🔗
<reference value="Patient/somaticPatient"/>
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<performedDateTime value="2023-02-02T01:01:10-06:00"/>
</Procedure>
IG © 2022+ HL7 International / Clinical Genomics. Package hl7.fhir.uv.genomics-reporting#3.0.0-ballot based on FHIR 4.0.1. Generated 2023-12-18
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