This page is part of the FHIR Specification (v5.0.0-ballot: R5 Ballot - see ballot notes). 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: 1 | Trial Use | Use Context: Not yet ready for Production use, Not yet ready for Production use |
This is a value set defined by the FHIR project.
Summary
Defining URL: | http://hl7.org/fhir/ValueSet/genomicstudy-type |
Version: | 5.0.0-ballot |
Name: | GenomicStudyType |
Title: | GenomicStudyType |
Status: | draft |
Definition: | The type of the GenomicStudy. |
Committee: | Clinical Genomics Work Group |
OID: | 2.16.840.1.113883.4.642.3.3082 (for OID based terminology systems) |
Flags: | Experimental |
This value set is used in the following places:
http://hl7.org/fhir/genomicstudy-type
This expansion generated 10 Sep 2022
This value set contains 12 concepts
Expansion based on GenomicStudyType v5.0.0-ballot (CodeSystem)
Code | System | Display | Definition |
alt-splc | http://hl7.org/fhir/genomicstudy-type | Alternative splicing detection | Identification of multiple different processed mRNA transcripts from the same DNA template |
chromatin | http://hl7.org/fhir/genomicstudy-type | Chromatin conformation | Analysis of the spacial organization of chromatin within a cell |
cnv | http://hl7.org/fhir/genomicstudy-type | CNV detection | 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 |
epi-alt-hist | http://hl7.org/fhir/genomicstudy-type | Epigenetic Alterations - histone modifications | Detection of biochemical modifications covalently bound to the N-terminal tail of a histone protein. These modifications may alter chromatin compaction and gene expression |
epi-alt-dna | http://hl7.org/fhir/genomicstudy-type | Epigenetic Alterations -DNA methylation | Detection of the presence of an additional methyl group on a DNA nucleobase, which may alter gene transcription |
fam-var-segr | http://hl7.org/fhir/genomicstudy-type | Familial variant segregation | Determining if a variant identified in an individual is present in other family members |
func-var | http://hl7.org/fhir/genomicstudy-type | Functional variation detection | Detection of sequence variants which may alter gene expression or gene product function when compared to the reference sequence |
gene-expression | http://hl7.org/fhir/genomicstudy-type | Gene expression profiling | Measurement and characterization of activity from all gene products |
post-trans-mod | http://hl7.org/fhir/genomicstudy-type | Post-translational Modification Identification | Detection of biochemical modifications covalently bound to the amino acid monomers of a processed protein |
snp | http://hl7.org/fhir/genomicstudy-type | SNP Detection | Determination of which nucleotide is base present at a known variable location of the genomic sequence |
str | http://hl7.org/fhir/genomicstudy-type | STR count | Quantification of the number of sequential microsatellite units in a repetitive sequence region |
struc-var | http://hl7.org/fhir/genomicstudy-type | Structural variation detection | Detection of deletions, insertions, or rearrangements of DNA segments compared to the reference sequence |
See the full registry of value sets defined as part of FHIR.
Explanation of the columns that may appear on this page:
Lvl | A few code lists that FHIR defines are hierarchical - each code is assigned a level. For value sets, levels are mostly used to organize codes for user convenience, but may follow code system hierarchy - see Code System for further information |
Source | The source of the definition of the code (when the value set draws in codes defined elsewhere) |
Code | The code (used as the code in the resource instance). If the code is in italics, this indicates that the code is not selectable ('Abstract') |
Display | The display (used in the display element of a Coding). If there is no display, implementers should not simply display the code, but map the concept into their application |
Definition | An explanation of the meaning of the concept |
Comments | Additional notes about how to use the code |