This page is part of the FHIR Specification (v5.0.0-ballot: FHIR R5 Ballot Preview). The current version which supercedes this 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 |
Raw JSON (canonical form + also see JSON Format Specification)
Definition for Code SystemGenomicStudyType
{ "resourceType" : "CodeSystem", "id" : "genomicstudy-type", "meta" : { "lastUpdated" : "2022-09-06T19:58:29.429-05:00", "profile" : ["http://hl7.org/fhir/StructureDefinition/shareablecodesystem"] }, "text" : { "status" : "generated", "div" : "<div>!-- Snipped for Brevity --></div>" }, "extension" : [{ "url" : "http://hl7.org/fhir/StructureDefinition/structuredefinition-wg", "valueCode" : "cg" }, { "url" : "http://hl7.org/fhir/StructureDefinition/structuredefinition-standards-status", "valueCode" : "trial-use" }, { "url" : "http://hl7.org/fhir/StructureDefinition/structuredefinition-fmm", "valueInteger" : 0 }], "url" : "http://hl7.org/fhir/genomicstudy-type", "identifier" : [{ "system" : "urn:ietf:rfc:3986", "value" : "urn:oid:2.16.840.1.113883.4.642.4.1975" }], "version" : "5.0.0-ballot", "name" : "GenomicStudyType", "title" : "GenomicStudyType", "status" : "draft", "experimental" : false, "date" : "2022-08-17T16:19:24-05:00", "publisher" : "HL7 (FHIR Project)", "contact" : [{ "telecom" : [{ "system" : "url", "value" : "http://hl7.org/fhir" }, { "system" : "email", "value" : "fhir@lists.hl7.org" }] }], "description" : "The type relevant to GenomicStudy.", "caseSensitive" : true, "valueSet" : "http://hl7.org/fhir/ValueSet/genomicstudy-type", "content" : "complete", "concept" : [{ "code" : "alt-splc", "display" : "Alternative splicing detection", "definition" : "Identification of multiple different processed mRNA transcripts from the same DNA template" }, { "code" : "chromatin", "display" : "Chromatin conformation", "definition" : "Analysis of the spacial organization of chromatin within a cell" }, { "code" : "cnv", "display" : "CNV detection", "definition" : "Detection of a change in the number of copies of a defined region of genomic DNA sequence resulting in structural variation when compared to the reference sequence" }, { "code" : "epi-alt-hist", "display" : "Epigenetic Alterations - histone modifications", "definition" : "Detection of biochemical modifications covalently bound to the N-terminal tail of a histone protein. These modifications may alter chromatin compaction and gene expression" }, { "code" : "epi-alt-dna", "display" : "Epigenetic Alterations -DNA methylation", "definition" : "Detection of the presence of an additional methyl group on a DNA nucleobase, which may alter gene transcription" }, { "code" : "fam-var-segr", "display" : "Familial variant segregation", "definition" : "Determining if a variant identified in an individual is present in other family members" }, { "code" : "func-var", "display" : "Functional variation detection", "definition" : "Detection of sequence variants which may alter gene expression or gene product function when compared to the reference sequence" }, { "code" : "gene-expression", "display" : "Gene expression profiling", "definition" : "Measurement and characterization of activity from all gene products" }, { "code" : "post-trans-mod", "display" : "Post-translational Modification Identification", "definition" : "Detection of biochemical modifications covalently bound to the amino acid monomers of a processed protein" }, { "code" : "snp", "display" : "SNP Detection", "definition" : "Determination of which nucleotide is base present at a known variable location of the genomic sequence" }, { "code" : "str", "display" : "STR count", "definition" : "Quantification of the number of sequential microsatellite units in a repetitive sequence region" }, { "code" : "struc-var", "display" : "Structural variation detection", "definition" : "Detection of deletions, insertions, or rearrangements of DNA segments compared to the reference 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.