Genomics Reporting Implementation Guide
3.0.0-ballot - Ballot International flag

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

: genomicstudyanalysis-trio2 - XML Representation

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<Procedure xmlns="http://hl7.org/fhir">
  <id value="genomicstudyanalysis-trio2"/>
  <meta>
    <profile
             value="http://hl7.org/fhir/uv/genomics-reporting/StructureDefinition/genomic-study-analysis"/>
  </meta>
  <text>
    <status value="extensions"/>
    <div xmlns="http://www.w3.org/1999/xhtml"><p><b>Generated Narrative: Procedure</b><a name="genomicstudyanalysis-trio2"> </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 &quot;genomicstudyanalysis-trio2&quot; </p><p style="margin-bottom: 0px">Profile: <a href="StructureDefinition-genomic-study-analysis.html">Genomic Study Analysis</a></p></div><p><b>Genomic Study Analysis Genome Build</b>: GRCh38 <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> (<a href="https://loinc.org/">LOINC</a>#LA26806-2)</span></p><p><b>Genomic Study Analysis Focus</b>: <a href="Patient-denovoFather.html">Patient/denovoFather</a> &quot; DENOVO&quot;</p><p><b>Genomic Study Analysis Focus</b>: <a href="Patient-denovoMother.html">Patient/denovoMother</a> &quot; DENOVO&quot;</p><p><b>Genomic Study Analysis Title</b>: Parental Sequence Variation Detection Using Next Generation Sequencing</p><p><b>Genomic Study Analysis Protocol Performed</b>: <a href="Procedure-SequencingProcedure.html">Procedure/SequencingProcedure</a></p><blockquote><p><b>Genomic Study Analysis Input</b></p><blockquote><p><b>url</b></p><code>file</code></blockquote><p><b>value</b>: <a href="DocumentReference-genomicFileProbandBAM.html">DocumentReference/genomicFileProbandBAM</a></p><blockquote><p><b>url</b></p><code>type</code></blockquote><p><b>value</b>: BAM <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> (<a href="CodeSystem-genomic-study-data-format-cs.html">Genomic Study Data Format CodeSystem</a>#bam)</span></p></blockquote><blockquote><p><b>Genomic Study Analysis Input</b></p><blockquote><p><b>url</b></p><code>file</code></blockquote><p><b>value</b>: <a href="DocumentReference-genomicFileMotherBAM.html">DocumentReference/genomicFileMotherBAM</a></p><blockquote><p><b>url</b></p><code>type</code></blockquote><p><b>value</b>: BAM <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> (<a href="CodeSystem-genomic-study-data-format-cs.html">Genomic Study Data Format CodeSystem</a>#bam)</span></p></blockquote><blockquote><p><b>Genomic Study Analysis Input</b></p><blockquote><p><b>url</b></p><code>file</code></blockquote><p><b>value</b>: <a href="DocumentReference-genomicFileFatherBAM.html">DocumentReference/genomicFileFatherBAM</a></p><blockquote><p><b>url</b></p><code>type</code></blockquote><p><b>value</b>: BAM <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> (<a href="CodeSystem-genomic-study-data-format-cs.html">Genomic Study Data Format CodeSystem</a>#bam)</span></p></blockquote><blockquote><p><b>Genomic Study Analysis Output</b></p><blockquote><p><b>url</b></p><code>file</code></blockquote><p><b>value</b>: <a href="DocumentReference-genomicFileProbandVCF.html">DocumentReference/genomicFileProbandVCF</a></p><blockquote><p><b>url</b></p><code>type</code></blockquote><p><b>value</b>: VCF <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> (<a href="CodeSystem-genomic-study-data-format-cs.html">Genomic Study Data Format CodeSystem</a>#vcf)</span></p></blockquote><p><b>instantiatesUri</b>: <a href="https://pubmed.ncbi.nlm.nih.gov/33927380/">https://pubmed.ncbi.nlm.nih.gov/33927380/</a></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-denovoChild.html">Patient/denovoChild</a> &quot; DENOVO&quot;</p><p><b>performed</b>: 2023-10-01</p></div>
  </text>
  <extension
             url="http://hl7.org/fhir/uv/genomics-reporting/StructureDefinition/genomic-study-analysis-genome-build">
    <valueCodeableConcept>
      <coding>
        <system value="http://loinc.org"/>
        <code value="LA26806-2"/>
        <display value="GRCh38"/>
      </coding>
    </valueCodeableConcept>
  </extension>
  <extension
             url="http://hl7.org/fhir/uv/genomics-reporting/StructureDefinition/genomic-study-analysis-focus">
    <valueReference>🔗 
      <reference value="Patient/denovoFather"/>
    </valueReference>
  </extension>
  <extension
             url="http://hl7.org/fhir/uv/genomics-reporting/StructureDefinition/genomic-study-analysis-focus">
    <valueReference>🔗 
      <reference value="Patient/denovoMother"/>
    </valueReference>
  </extension>
  <extension
             url="http://hl7.org/fhir/uv/genomics-reporting/StructureDefinition/genomic-study-analysis-title">
    <valueString
                 value="Parental Sequence Variation Detection Using Next Generation Sequencing"/>
  </extension>
  <extension
             url="http://hl7.org/fhir/uv/genomics-reporting/StructureDefinition/genomic-study-analysis-protocol-performed">
    <valueReference>🔗 
      <reference value="Procedure/SequencingProcedure"/>
    </valueReference>
  </extension>
  <extension
             url="http://hl7.org/fhir/uv/genomics-reporting/StructureDefinition/genomic-study-analysis-input">
    <extension url="file">
      <valueReference>🔗 
        <reference value="DocumentReference/genomicFileProbandBAM"/>
      </valueReference>
    </extension>
    <extension url="type">
      <valueCodeableConcept>
        <coding>
          <system
                  value="http://hl7.org/fhir/uv/genomics-reporting/CodeSystem/genomic-study-data-format-cs"/>
          <code value="bam"/>
          <display value="BAM"/>
        </coding>
      </valueCodeableConcept>
    </extension>
  </extension>
  <extension
             url="http://hl7.org/fhir/uv/genomics-reporting/StructureDefinition/genomic-study-analysis-input">
    <extension url="file">
      <valueReference>🔗 
        <reference value="DocumentReference/genomicFileMotherBAM"/>
      </valueReference>
    </extension>
    <extension url="type">
      <valueCodeableConcept>
        <coding>
          <system
                  value="http://hl7.org/fhir/uv/genomics-reporting/CodeSystem/genomic-study-data-format-cs"/>
          <code value="bam"/>
          <display value="BAM"/>
        </coding>
      </valueCodeableConcept>
    </extension>
  </extension>
  <extension
             url="http://hl7.org/fhir/uv/genomics-reporting/StructureDefinition/genomic-study-analysis-input">
    <extension url="file">
      <valueReference>🔗 
        <reference value="DocumentReference/genomicFileFatherBAM"/>
      </valueReference>
    </extension>
    <extension url="type">
      <valueCodeableConcept>
        <coding>
          <system
                  value="http://hl7.org/fhir/uv/genomics-reporting/CodeSystem/genomic-study-data-format-cs"/>
          <code value="bam"/>
          <display value="BAM"/>
        </coding>
      </valueCodeableConcept>
    </extension>
  </extension>
  <extension
             url="http://hl7.org/fhir/uv/genomics-reporting/StructureDefinition/genomic-study-analysis-output">
    <extension url="file">
      <valueReference>🔗 
        <reference value="DocumentReference/genomicFileProbandVCF"/>
      </valueReference>
    </extension>
    <extension url="type">
      <valueCodeableConcept>
        <coding>
          <system
                  value="http://hl7.org/fhir/uv/genomics-reporting/CodeSystem/genomic-study-data-format-cs"/>
          <code value="vcf"/>
          <display value="VCF"/>
        </coding>
      </valueCodeableConcept>
    </extension>
  </extension>
  <instantiatesUri value="https://pubmed.ncbi.nlm.nih.gov/33927380/"/>
  <status value="completed"/>
  <category>
    <coding>
      <system
              value="http://terminology.hl7.org/CodeSystem/observation-category"/>
      <code value="laboratory"/>
    </coding>
  </category>
  <subject>🔗 
    <reference value="Patient/denovoChild"/>
  </subject>
  <performedDateTime value="2023-10-01"/>
</Procedure>