This is the Continuous Integration Build of FHIR (will be incorrect/inconsistent at times).
See the Directory of published versions
Clinical Genomics Work Group | Maturity Level: N/A | Standards Status: Informative | Compartments: Patient |
Raw JSON (canonical form + also see JSON Format Specification)
GenomicStudy - Lung mass - sequencing analysis
{ "resourceType" : "GenomicStudy", "id" : "example-lungMass", "identifier" : [{ "use" : "temp", "system" : "http://www.somesystemabc.net/identifiers/genomicstudies", "value" : "urn:uuid:1111-1111-1111-1112" }], "status" : "registered", "type" : [{ "coding" : [{ "system" : "http://snomed.info/sct", "code" : "443968007", "display" : "Sequencing of entire coding region of gene (procedure)" }] }], "subject" : { "reference" : "Patient/genomicPatient" }, "encounter" : { "reference" : "Encounter/genomicEncounter" }, "startDate" : "2019-03-01", "basedOn" : [{ "reference" : "ServiceRequest/genomicServiceRequest2" }], "referrer" : { "reference" : "Practitioner/practitioner01" }, "interpreter" : [{ "reference" : "Practitioner/practitioner02" }], "reason" : [{ "concept" : { "coding" : [{ "system" : "http://snomed.info/sct", "code" : "309529002", "display" : "Lung mass (finding)" }] } }], "note" : [{ "text" : "For technical reasons, PIK3CB was deemed uncallable." }], "description" : "Whole exome sequencing of lung biopsy. 300 genes are examined for simple variants (SNV, MNV, InDel), and 170 genes are also examined for CNVs. For technical reasons, PIK3CB was deemed uncallable.", "analysis" : [{ "identifier" : [{ "use" : "official", "system" : "http://www.somesystemabc.net/identifiers/genomicAnalyses", "value" : "urn:uuid:1111-1111-1111-1112" }], "methodType" : [{ "coding" : [{ "system" : "http://snomed.info/sct", "code" : "117040002", "display" : "Nucleic acid sequencing (procedure)" }] }], "changeType" : [{ "coding" : [{ "system" : "http://sequenceontology.org", "code" : "SO:0001483", "display" : "SNV" }] }, { "coding" : [{ "system" : "http://sequenceontology.org", "code" : "SO:0002007", "display" : "MNV" }] }, { "coding" : [{ "system" : "http://sequenceontology.org", "code" : "SO:1000032", "display" : "delins" }] }], "genomeBuild" : { "coding" : [{ "system" : "http://loinc.org", "code" : "LA26806-2", "display" : "GRCh38" }] }, "title" : "Simple variant analysis", "specimen" : [{ "reference" : "Specimen/genomicSpecimen" }], "date" : "2019-03-01T01:01:10-06:00", "note" : [{ "text" : "For technical reasons, PIK3CB was deemed uncallable using this method." }], "regionsStudied" : [{ "reference" : "DocumentReference/WES_FullSequencedRegion_GRCh38" }], "regionsCalled" : [{ "reference" : "DocumentReference/SimpleVariantAnalysis_called" }], "output" : [{ "file" : { "reference" : "DocumentReference/genomicVCFfile_simple" }, "type" : { "coding" : [{ "code" : "vcf", "display" : "VCF" }] } }], "performer" : [{ "actor" : { "reference" : "Practitioner/practitioner02" }, "role" : { "coding" : [{ "system" : "http://terminology.hl7.org/3.1.0/CodeSystem-v3-ParticipationType.html", "code" : "PRF", "display" : "Performer" }] } }], "device" : [{ "device" : { "reference" : "Device/NGS-device" }, "function" : { "coding" : [{ "display" : "Next Generation Sequencing" }] } }] }, { "identifier" : [{ "use" : "official", "system" : "http://www.somesystemabc.net/identifiers/genomicAnalyses", "value" : "urn:uuid:1111-1111-1111-1115" }], "methodType" : [{ "coding" : [{ "system" : "http://snomed.info/sct", "code" : "117040002", "display" : "Nucleic acid sequencing (procedure)" }] }], "changeType" : [{ "coding" : [{ "system" : "http://sequenceontology.org", "code" : "SO:0001019", "display" : "CNV" }] }], "genomeBuild" : { "coding" : [{ "system" : "http://loinc.org", "code" : "LA26806-2", "display" : "GRCh38" }] }, "title" : "CNV analysis", "specimen" : [{ "reference" : "Specimen/genomicSpecimen" }], "date" : "2019-03-01T01:01:10-06:00", "note" : [{ "text" : "For technical reasons, PIK3CB was deemed uncallable using this method." }], "regionsStudied" : [{ "reference" : "DocumentReference/WES_FullSequencedRegion_GRCh38" }], "regionsCalled" : [{ "reference" : "DocumentReference/CNVAnalysis_called" }], "output" : [{ "file" : { "reference" : "DocumentReference/genomicVCFfile_cnv" }, "type" : { "coding" : [{ "code" : "vcf", "display" : "VCF" }] } }], "performer" : [{ "actor" : { "reference" : "Practitioner/practitioner02" }, "role" : { "coding" : [{ "system" : "http://terminology.hl7.org/3.1.0/CodeSystem-v3-ParticipationType.html", "code" : "PRF", "display" : "Performer" }] } }] }] }
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-ballot2 generated on Fri, Nov 15, 2024 17:50+0000.
Links: Search |
Version History |
Contents |
Glossary |
QA |
Compare to R5 |
|
Propose a change