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.