This page is part of the FHIR Specification v6.0.0-ballot1: Release 6 Ballot (1st Draft) (see Ballot Notes). The current version is 5.0.0. For a full list of available versions, see the Directory of published versions
Clinical Genomics Work Group | Maturity Level: N/A | Standards Status: Informative | Compartments: Patient |
Raw XML (canonical form + also see XML Format Specification)
GenomicStudy - Trio study - De novo mutation 1 (id = "example")
<?xml version="1.0" encoding="UTF-8"?> <GenomicStudy xmlns="http://hl7.org/fhir"> <!-- from Resource: id, meta, implicitRules, and language --> <id value="example"/> <!-- from DomainResource: text, contained, extension, and modifierExtension --> <text> <status value="additional"/> <div xmlns="http://www.w3.org/1999/xhtml">This is a genomic study that involves a de novo mutation analysis of a proband, mother, and father. The analysis involves the use use of NGS device and a specilized analysis platform.</div> </text> <identifier> <use value="temp"/> <system value="http://www.somesystemabc.net/identifiers/genomicstudies"/> <value value="urn:uuid:1111-1111-1111-1111"/> </identifier> <status value="unknown"/> <type> <coding> <system value="http://hl7.org/fhir/genomicstudy-type"/> <code value="fam-var-segr"/> <display value="Familial variant segregation"/> </coding> </type> <subject> <reference value="Patient/denovoChild"/> </subject> <encounter> <reference value="Encounter/denovoEncounter"/> </encounter> <startDate value="2021-01-01"/> <basedOn> <reference value="ServiceRequest/genomicServiceRequest"/> </basedOn> <referrer> <reference value="Practitioner/practitioner01"/> </referrer> <interpreter> <reference value="Practitioner/practitioner02"/> </interpreter> <reason> <concept> <coding> <system value="http://snomed.info/sct"/> <code value="267431006"/> <display value="Disorder of lipid metabolism (disorder)"/> </coding> </concept> </reason> <note> <text value="This de novo mutation is urgent and important for establishing the treatment plan."/> </note> <description value="De novo mutation study of the patient."/> <analysis> <!-- 0..* Genomic Analysis Event of proband --> <identifier> <use value="temp"/> <system value="http://www.somesystemabc.net/identifiers/genomicAnalyses"/> <value value="urn:uuid:1111-1111-1111-1111"/> </identifier> <!-- <instantiatesCanonical>0..1 canonical(PlanDefinition) The defined protocol that describes the analysis</instantiatesCanonical> --> <instantiatesUri value="https://pubmed.ncbi.nlm.nih.gov/33927380/"/> <title value="Proband Sequence Variation Detection Using Next Generation Sequencing"/> <specimen> <reference value="Specimen/denovo-1"/> </specimen> <date value="2021-01-01T01:01:10-06:00"/> <!-- 0..1 The date of the analysis event --> <note> <text value="This is a next generation sequencing analysis of a proband."/> </note> <!-- <protocolPerformed>0..1 Reference(Procedure|Task) The protocol that was performed for the analysis event</protocolPerformed> --> <!-- <regionsCalled>0..1 Reference(DocumentReference) Genomic regions actually called in the analysis event (BED file)</regionsCalled> --> <input> <!-- 0..* Inputs for the analysis event of Child --> <file> <reference value="DocumentReference/genomicFile1"/> </file> <type> <coding> <code value="vcf"/> <display value="VCF"/> </coding> </type> <!-- <generatedBy[x]>0..1 Identifier|Reference(GenomicStudy) The analysis event or other GenomicStudy that generated this input file</generatedBy[x]> --> </input> <performer> <!-- 0..* Performer for the analysis event --> <actor> <reference value="Practitioner/practitioner02"/> </actor> <role> <coding> <system value="http://terminology.hl7.org/3.1.0/CodeSystem-v3-ParticipationType.html"/> <code value="PRF"/> <display value="Performer"/> </coding> </role> </performer> <device> <!-- 0..* Devices used for the analysis (e.g., instruments, software), with settings and parameters --> <device> <reference value="Device/NGS-device"/> </device> <function> <coding> <display value="Next Generation Sequencing"/> </coding> </function> </device> </analysis> <analysis> <!-- 0..* Genomic Analysis Event of mother --> <identifier> <use value="temp"/> <system value="http://www.somesystemabc.net/identifiers/genomicAnalyses"/> <value value="urn:uuid:1111-1111-1111-1112"/> </identifier> <!-- <instantiatesCanonical>0..1 canonical(PlanDefinition) The defined protocol that describes the analysis</instantiatesCanonical> --> <instantiatesUri value="https://pubmed.ncbi.nlm.nih.gov/33927380/"/> <title value="Maternal Sequence Variation Detection Using Next Generation Sequencing"/> <!-- 0..1 Name of the analysis event (human friendly) --> <focus> <reference value="Patient/denovoMother"/> </focus> <specimen> <reference value="Specimen/denovo-2"/> </specimen> <date value="2021-01-01T01:01:10-06:00"/> <!-- 0..1 The date of the analysis event --> <note> <text value="This is a next generation sequencing analysis of a mother of a proband."/> </note> <input> <!-- 0..* Inputs for the analysis event of Mother --> <file> <reference value="DocumentReference/genomicFile2"/> </file> <type> <coding> <code value="vcf"/> <display value="VCF"/> </coding> </type> <!-- <generatedBy[x]>0..1 Identifier|Reference(GenomicStudy) The analysis event or other GenomicStudy that generated this input file</generatedBy[x]> --> </input> <performer> <!-- 0..* Performer for the analysis event --> <actor> <reference value="Practitioner/practitioner02"/> </actor> <role> <coding> <system value="http://terminology.hl7.org/3.1.0/CodeSystem-v3-ParticipationType.html"/> <code value="PRF"/> <display value="Performer"/> </coding> </role> </performer> <device> <!-- 0..* Devices used for the analysis (e.g., instruments, software), with settings and parameters --> <device> <reference value="Device/NGS-device"/> </device> <!-- <function>0..1 CodeableConcept Specific function for the device used for the analysis</function> --> </device> </analysis> <analysis> <!-- 0..* Genomic Analysis Event of father --> <identifier> <use value="temp"/> <system value="http://www.somesystemabc.net/identifiers/genomicAnalyses"/> <value value="urn:uuid:1111-1111-1111-1113"/> </identifier> <!-- <instantiatesCanonical>0..1 canonical(PlanDefinition) The defined protocol that describes the analysis</instantiatesCanonical> --> <instantiatesUri value="https://pubmed.ncbi.nlm.nih.gov/33927380/"/> <title value="Paternal Sequence Variation Detection Using Next Generation Sequencing"/> <focus> <reference value="Patient/denovoFather"/> </focus> <specimen> <reference value="Specimen/denovo-3"/> </specimen> <date value="2021-01-01T01:01:10-06:00"/> <!-- 0..1 The date of the analysis event --> <note> <text value="This is a next generation sequencing analysis of a father of a proband."/> </note> <input> <!-- 0..* Inputs for the analysis event --> <file> <reference value="DocumentReference/genomicFile3"/> </file> <type> <coding> <code value="vcf"/> <display value="VCF"/> </coding> </type> <!-- <generatedBy[x]>0..1 Identifier|Reference(GenomicStudy) The analysis event or other GenomicStudy that generated this input file</generatedBy[x]> --> </input> <performer> <!-- 0..* Performer for the analysis event --> <actor> <reference value="Practitioner/practitioner02"/> </actor> <role> <coding> <system value="http://terminology.hl7.org/3.1.0/CodeSystem-v3-ParticipationType.html"/> <code value="PRF"/> <display value="Performer"/> </coding> </role> </performer> <device> <!-- 0..* Devices used for the analysis (e.g., instruments, software), with settings and parameters --> <device> <reference value="Device/NGS-device"/> </device> <!-- <function>0..1 CodeableConcept Specific function for the device used for the analysis</function> --> </device> </analysis> <analysis> <!-- 0..* De Novo Mutation Analysis --> <identifier> <use value="temp"/> <system value="http://www.somesystemabc.net/identifiers/genomicAnalyses"/> <value value="urn:uuid:1111-1111-1111-1114"/> </identifier> <!-- <instantiatesCanonical>0..1 canonical(PlanDefinition) The defined protocol that describes the analysis</instantiatesCanonical> --> <instantiatesUri value="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6885382/"/> <title value="De Novo Mutation Detection and Interpretation"/> <!-- <specimen> 0..1 Reference(Specimen) The specimen used in the analysis event</specimen> --> <date value="2021-01-01T03:01:10-06:00"/> <!-- 0..1 The date of the analysis event --> <note> <text value="This is a next generation sequencing analysis of the comparison analysis of proband and parents sequences."/> </note> <input> <!-- 0..* Inputs for the analysis event of Child --> <file> <reference value="DocumentReference/genomicFile1"/> </file> <type> <coding> <code value="vcf"/> <display value="VCF"/> </coding> </type> <!-- <generatedBy[x]>0..1 Identifier|Reference(GenomicStudy) The analysis event or other GenomicStudy that generated this input file</generatedBy[x]> --> </input> <input> <!-- 0..* Inputs for the analysis event of Mother --> <file> <reference value="DocumentReference/genomicFile2"/> </file> <type> <coding> <code value="vcf"/> <display value="VCF"/> </coding> </type> <!-- <generatedBy[x]>0..1 Identifier|Reference(GenomicStudy) The analysis event or other GenomicStudy that generated this input file</generatedBy[x]> --> </input> <input> <!-- 0..* Inputs for the analysis event of Father --> <file> <reference value="DocumentReference/genomicFile3"/> </file> <type> <coding> <code value="vcf"/> <display value="VCF"/> </coding> </type> <!-- <generatedBy[x]>0..1 Identifier|Reference(GenomicStudy) The analysis event or other GenomicStudy that generated this input file</generatedBy[x]> --> </input> <performer> <!-- 0..* Performer for the analysis event --> <actor> <reference value="Practitioner/practitioner02"/> </actor> <role> <coding> <system value="http://terminology.hl7.org/3.1.0/CodeSystem-v3-ParticipationType.html"/> <code value="PRF"/> <display value="Performer"/> </coding> </role> </performer> <device> <!-- 0..* Devices used for the analysis (e.g., instruments, software), with settings and parameters --> <device> <reference value="Device/Triodenovo-SW"/> </device> <!-- <function>0..1 CodeableConcept Specific function for the device used for the analysis</function> --> </device> </analysis> </GenomicStudy>
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.
FHIR ®© HL7.org 2011+. FHIR R6 hl7.fhir.core#6.0.0-ballot1 generated on Mon, Dec 18, 2023 15:17+1100.
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