Genomics Reporting Implementation Guide
3.0.1-SNAPSHOT - Ballot International flag

Genomics Reporting Implementation Guide, published by HL7 International / Clinical Genomics. This guide is not an authorized publication; it is the continuous build for version 3.0.1-SNAPSHOT built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/HL7/genomics-reporting/ and changes regularly. See the Directory of published versions

: Genomic Study Method Type CodeSystem - TTL Representation

Active as of 2024-04-09

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@prefix fhir: <http://hl7.org/fhir/> .
@prefix owl: <http://www.w3.org/2002/07/owl#> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .

# - resource -------------------------------------------------------------------

 a fhir:CodeSystem ;
  fhir:nodeRole fhir:treeRoot ;
  fhir:id [ fhir:v "genomic-study-method-type-cs"] ; # 
  fhir:text [
fhir:status [ fhir:v "generated" ] ;
fhir:div "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p>This case-sensitive code system <code>http://hl7.org/fhir/uv/genomics-reporting/CodeSystem/genomic-study-method-type-cs</code> defines the following codes:</p><table class=\"codes\"><tr><td style=\"white-space:nowrap\"><b>Code</b></td><td><b>Display</b></td></tr><tr><td style=\"white-space:nowrap\">biochemical-genetics<a name=\"genomic-study-method-type-cs-biochemical-genetics\"> </a></td><td>Biochemical Genetics</td></tr><tr><td style=\"white-space:nowrap\">cytogenetics<a name=\"genomic-study-method-type-cs-cytogenetics\"> </a></td><td>Cytogenetics</td></tr><tr><td style=\"white-space:nowrap\">molecular-genetics<a name=\"genomic-study-method-type-cs-molecular-genetics\"> </a></td><td>Molecular Genetics</td></tr><tr><td style=\"white-space:nowrap\">analyte<a name=\"genomic-study-method-type-cs-analyte\"> </a></td><td>Analyte</td></tr><tr><td style=\"white-space:nowrap\">chromosome-breakage-studies<a name=\"genomic-study-method-type-cs-chromosome-breakage-studies\"> </a></td><td>Chromosome breakage studies</td></tr><tr><td style=\"white-space:nowrap\">deletion-duplication-analysis<a name=\"genomic-study-method-type-cs-deletion-duplication-analysis\"> </a></td><td>Deletion/duplication analysis</td></tr><tr><td style=\"white-space:nowrap\">detection-of-homozygosity<a name=\"genomic-study-method-type-cs-detection-of-homozygosity\"> </a></td><td>Detection of homozygosity</td></tr><tr><td style=\"white-space:nowrap\">enzyme-assay<a name=\"genomic-study-method-type-cs-enzyme-assay\"> </a></td><td>Enzyme assay</td></tr><tr><td style=\"white-space:nowrap\">fish-interphase<a name=\"genomic-study-method-type-cs-fish-interphase\"> </a></td><td>FISH-interphase</td></tr><tr><td style=\"white-space:nowrap\">fish-metaphase<a name=\"genomic-study-method-type-cs-fish-metaphase\"> </a></td><td>FISH-metaphase</td></tr><tr><td style=\"white-space:nowrap\">flow-cytometry<a name=\"genomic-study-method-type-cs-flow-cytometry\"> </a></td><td>Flow cytometry</td></tr><tr><td style=\"white-space:nowrap\">fish<a name=\"genomic-study-method-type-cs-fish\"> </a></td><td>Fluorescence in situ hybridization (FISH)</td></tr><tr><td style=\"white-space:nowrap\">immunohistochemistry<a name=\"genomic-study-method-type-cs-immunohistochemistry\"> </a></td><td>Immunohistochemistry</td></tr><tr><td style=\"white-space:nowrap\">karyotyping<a name=\"genomic-study-method-type-cs-karyotyping\"> </a></td><td>Karyotyping</td></tr><tr><td style=\"white-space:nowrap\">linkage-analysis<a name=\"genomic-study-method-type-cs-linkage-analysis\"> </a></td><td>Linkage analysis</td></tr><tr><td style=\"white-space:nowrap\">methylation-analysis<a name=\"genomic-study-method-type-cs-methylation-analysis\"> </a></td><td>Methylation analysis</td></tr><tr><td style=\"white-space:nowrap\">msi<a name=\"genomic-study-method-type-cs-msi\"> </a></td><td>Microsatellite instability testing (MSI)</td></tr><tr><td style=\"white-space:nowrap\">m-fish<a name=\"genomic-study-method-type-cs-m-fish\"> </a></td><td>Multicolor FISH (M-FISH)</td></tr><tr><td style=\"white-space:nowrap\">mutation-scanning-of-select-exons<a name=\"genomic-study-method-type-cs-mutation-scanning-of-select-exons\"> </a></td><td>Mutation scanning of select exons</td></tr><tr><td style=\"white-space:nowrap\">mutation-scanning-of-the-entire-coding-region<a name=\"genomic-study-method-type-cs-mutation-scanning-of-the-entire-coding-region\"> </a></td><td>Mutation scanning of the entire coding region</td></tr><tr><td style=\"white-space:nowrap\">protein-analysis<a name=\"genomic-study-method-type-cs-protein-analysis\"> </a></td><td>Protein analysis</td></tr><tr><td style=\"white-space:nowrap\">protein-expression<a name=\"genomic-study-method-type-cs-protein-expression\"> </a></td><td>Protein expression</td></tr><tr><td style=\"white-space:nowrap\">rna-analysis<a name=\"genomic-study-method-type-cs-rna-analysis\"> </a></td><td>RNA analysis</td></tr><tr><td style=\"white-space:nowrap\">sequence-analysis-of-select-exons<a name=\"genomic-study-method-type-cs-sequence-analysis-of-select-exons\"> </a></td><td>Sequence analysis of select exons</td></tr><tr><td style=\"white-space:nowrap\">sequence-analysis-of-the-entire-coding-region<a name=\"genomic-study-method-type-cs-sequence-analysis-of-the-entire-coding-region\"> </a></td><td>Sequence analysis of the entire coding region</td></tr><tr><td style=\"white-space:nowrap\">sister-chromatid-exchange<a name=\"genomic-study-method-type-cs-sister-chromatid-exchange\"> </a></td><td>Sister chromatid exchange</td></tr><tr><td style=\"white-space:nowrap\">targeted-variant-analysis<a name=\"genomic-study-method-type-cs-targeted-variant-analysis\"> </a></td><td>Targeted variant analysis</td></tr><tr><td style=\"white-space:nowrap\">udp<a name=\"genomic-study-method-type-cs-udp\"> </a></td><td>Uniparental disomy study (UPD)</td></tr><tr><td style=\"white-space:nowrap\">aspe<a name=\"genomic-study-method-type-cs-aspe\"> </a></td><td>Allele-specific primer extension (ASPE)</td></tr><tr><td style=\"white-space:nowrap\">alternative-splicing-detection<a name=\"genomic-study-method-type-cs-alternative-splicing-detection\"> </a></td><td>Alternative splicing detection</td></tr><tr><td style=\"white-space:nowrap\">bi-directional-sanger-sequence-analysis<a name=\"genomic-study-method-type-cs-bi-directional-sanger-sequence-analysis\"> </a></td><td>Bi-directional Sanger Sequence Analysis</td></tr><tr><td style=\"white-space:nowrap\">c-banding<a name=\"genomic-study-method-type-cs-c-banding\"> </a></td><td>C-banding</td></tr><tr><td style=\"white-space:nowrap\">cia<a name=\"genomic-study-method-type-cs-cia\"> </a></td><td>Chemiluminescent Immunoassay (CIA)</td></tr><tr><td style=\"white-space:nowrap\">chromatin-immunoprecipitation-on-chip<a name=\"genomic-study-method-type-cs-chromatin-immunoprecipitation-on-chip\"> </a></td><td>Chromatin Immunoprecipitation on ChIP</td></tr><tr><td style=\"white-space:nowrap\">comparative-genomic-hybridization<a name=\"genomic-study-method-type-cs-comparative-genomic-hybridization\"> </a></td><td>Comparative Genomic Hybridization</td></tr><tr><td style=\"white-space:nowrap\">damid<a name=\"genomic-study-method-type-cs-damid\"> </a></td><td>DamID</td></tr><tr><td style=\"white-space:nowrap\">digital-virtual-karyotyping<a name=\"genomic-study-method-type-cs-digital-virtual-karyotyping\"> </a></td><td>Digital / Virtual karyotyping</td></tr><tr><td style=\"white-space:nowrap\">digital-microfluidic-microspheres<a name=\"genomic-study-method-type-cs-digital-microfluidic-microspheres\"> </a></td><td>Digital microfluidic microspheres</td></tr><tr><td style=\"white-space:nowrap\">enzymatic-levels<a name=\"genomic-study-method-type-cs-enzymatic-levels\"> </a></td><td>Enzymatic levels</td></tr><tr><td style=\"white-space:nowrap\">enzyme-activity<a name=\"genomic-study-method-type-cs-enzyme-activity\"> </a></td><td>Enzyme activity</td></tr><tr><td style=\"white-space:nowrap\">elisa<a name=\"genomic-study-method-type-cs-elisa\"> </a></td><td>Enzyme-Linked Immunosorbent Assays (ELISA)</td></tr><tr><td style=\"white-space:nowrap\">fluorometry<a name=\"genomic-study-method-type-cs-fluorometry\"> </a></td><td>Fluorometry</td></tr><tr><td style=\"white-space:nowrap\">fusion-genes-microarrays<a name=\"genomic-study-method-type-cs-fusion-genes-microarrays\"> </a></td><td>Fusion genes microarrays</td></tr><tr><td style=\"white-space:nowrap\">g-banding<a name=\"genomic-study-method-type-cs-g-banding\"> </a></td><td>G-banding</td></tr><tr><td style=\"white-space:nowrap\">gc-ms<a name=\"genomic-study-method-type-cs-gc-ms\"> </a></td><td>Gas chromatographymass spectrometry (GC-MS)</td></tr><tr><td style=\"white-space:nowrap\">gene-expression-profiling<a name=\"genomic-study-method-type-cs-gene-expression-profiling\"> </a></td><td>Gene expression profiling</td></tr><tr><td style=\"white-space:nowrap\">gene-id<a name=\"genomic-study-method-type-cs-gene-id\"> </a></td><td>GeneID</td></tr><tr><td style=\"white-space:nowrap\">gold-nanoparticle-probe-technology<a name=\"genomic-study-method-type-cs-gold-nanoparticle-probe-technology\"> </a></td><td>Gold nanoparticle probe technology</td></tr><tr><td style=\"white-space:nowrap\">hplc<a name=\"genomic-study-method-type-cs-hplc\"> </a></td><td>High-performance liquid chromatography (HPLC)</td></tr><tr><td style=\"white-space:nowrap\">lc-ms<a name=\"genomic-study-method-type-cs-lc-ms\"> </a></td><td>Liquid chromatography mass spectrometry (LC-MS)</td></tr><tr><td style=\"white-space:nowrap\">lc-ms-ms<a name=\"genomic-study-method-type-cs-lc-ms-ms\"> </a></td><td>Liquid chromatography-tandem mass spectrometry (LC-MS/MS)</td></tr><tr><td style=\"white-space:nowrap\">metabolite-levels<a name=\"genomic-study-method-type-cs-metabolite-levels\"> </a></td><td>Metabolite levels</td></tr><tr><td style=\"white-space:nowrap\">methylation-specific-pcr<a name=\"genomic-study-method-type-cs-methylation-specific-pcr\"> </a></td><td>Methylation-specific PCR</td></tr><tr><td style=\"white-space:nowrap\">microarray<a name=\"genomic-study-method-type-cs-microarray\"> </a></td><td>Microarray</td></tr><tr><td style=\"white-space:nowrap\">mlpa<a name=\"genomic-study-method-type-cs-mlpa\"> </a></td><td>Multiplex Ligation-dependent Probe Amplification (MLPA)</td></tr><tr><td style=\"white-space:nowrap\">ngs-mps<a name=\"genomic-study-method-type-cs-ngs-mps\"> </a></td><td>Next-Generation (NGS)/Massively parallel sequencing (MPS)</td></tr><tr><td style=\"white-space:nowrap\">ola<a name=\"genomic-study-method-type-cs-ola\"> </a></td><td>Oligonucleotide Ligation Assay (OLA)</td></tr><tr><td style=\"white-space:nowrap\">oligonucleotide-hybridization-based-dna-sequencing<a name=\"genomic-study-method-type-cs-oligonucleotide-hybridization-based-dna-sequencing\"> </a></td><td>Oligonucleotide hybridization-based DNA sequencing</td></tr><tr><td style=\"white-space:nowrap\">other<a name=\"genomic-study-method-type-cs-other\"> </a></td><td>Other</td></tr><tr><td style=\"white-space:nowrap\">pcr<a name=\"genomic-study-method-type-cs-pcr\"> </a></td><td>PCR</td></tr><tr><td style=\"white-space:nowrap\">pcr-with-allele-specific-hybridization<a name=\"genomic-study-method-type-cs-pcr-with-allele-specific-hybridization\"> </a></td><td>PCR with allele specific hybridization</td></tr><tr><td style=\"white-space:nowrap\">pcr-rflp-with-southern-hybridization<a name=\"genomic-study-method-type-cs-pcr-rflp-with-southern-hybridization\"> </a></td><td>PCR-RFLP with Southern hybridization</td></tr><tr><td style=\"white-space:nowrap\">protein-truncation-test<a name=\"genomic-study-method-type-cs-protein-truncation-test\"> </a></td><td>Protein truncation test</td></tr><tr><td style=\"white-space:nowrap\">pyrosequencing<a name=\"genomic-study-method-type-cs-pyrosequencing\"> </a></td><td>Pyrosequencing</td></tr><tr><td style=\"white-space:nowrap\">q-banding<a name=\"genomic-study-method-type-cs-q-banding\"> </a></td><td>Q-banding</td></tr><tr><td style=\"white-space:nowrap\">qpcr<a name=\"genomic-study-method-type-cs-qpcr\"> </a></td><td>Quantitative PCR (qPCR)</td></tr><tr><td style=\"white-space:nowrap\">r-banding<a name=\"genomic-study-method-type-cs-r-banding\"> </a></td><td>R-banding</td></tr><tr><td style=\"white-space:nowrap\">rflp<a name=\"genomic-study-method-type-cs-rflp\"> </a></td><td>RFLP</td></tr><tr><td style=\"white-space:nowrap\">rt-lamp<a name=\"genomic-study-method-type-cs-rt-lamp\"> </a></td><td>RT-LAMP</td></tr><tr><td style=\"white-space:nowrap\">rt-pcr<a name=\"genomic-study-method-type-cs-rt-pcr\"> </a></td><td>RT-PCR</td></tr><tr><td style=\"white-space:nowrap\">rt-pcr-with-gel-analysis<a name=\"genomic-study-method-type-cs-rt-pcr-with-gel-analysis\"> </a></td><td>RT-PCR with gel analysis</td></tr><tr><td style=\"white-space:nowrap\">rt-qpcr<a name=\"genomic-study-method-type-cs-rt-qpcr\"> </a></td><td>RT-qPCR</td></tr><tr><td style=\"white-space:nowrap\">snp-detection<a name=\"genomic-study-method-type-cs-snp-detection\"> </a></td><td>SNP Detection</td></tr><tr><td style=\"white-space:nowrap\">silver-staining<a name=\"genomic-study-method-type-cs-silver-staining\"> </a></td><td>Silver staining</td></tr><tr><td style=\"white-space:nowrap\">sky<a name=\"genomic-study-method-type-cs-sky\"> </a></td><td>Spectral karyotyping (SKY)</td></tr><tr><td style=\"white-space:nowrap\">t-banding<a name=\"genomic-study-method-type-cs-t-banding\"> </a></td><td>T-banding</td></tr><tr><td style=\"white-space:nowrap\">ms-ms<a name=\"genomic-study-method-type-cs-ms-ms\"> </a></td><td>Tandem mass spectrometry (MS/MS)</td></tr><tr><td style=\"white-space:nowrap\">tetra-nucleotide-repeat-by-pcr-or-southern-blot<a name=\"genomic-study-method-type-cs-tetra-nucleotide-repeat-by-pcr-or-southern-blot\"> </a></td><td>Tetra-nucleotide repeat by PCR or Southern Blot</td></tr><tr><td style=\"white-space:nowrap\">tiling-arrays<a name=\"genomic-study-method-type-cs-tiling-arrays\"> </a></td><td>Tiling Arrays</td></tr><tr><td style=\"white-space:nowrap\">trinucleotide-repeat-by-pcr-or-southern-blot<a name=\"genomic-study-method-type-cs-trinucleotide-repeat-by-pcr-or-southern-blot\"> </a></td><td>Trinucleotide repeat by PCR or Southern Blot</td></tr><tr><td style=\"white-space:nowrap\">uni-directional-sanger-sequencing<a name=\"genomic-study-method-type-cs-uni-directional-sanger-sequencing\"> </a></td><td>Uni-directional Sanger sequencing</td></tr></table></div>"
  ] ; # 
  fhir:extension ( [
fhir:url [ fhir:v "http://hl7.org/fhir/StructureDefinition/structuredefinition-wg"^^xsd:anyURI ] ;
fhir:value [ fhir:v "cg" ]
  ] ) ; # 
  fhir:url [ fhir:v "http://hl7.org/fhir/uv/genomics-reporting/CodeSystem/genomic-study-method-type-cs"^^xsd:anyURI] ; # 
  fhir:version [ fhir:v "3.0.1-SNAPSHOT"] ; # 
  fhir:name [ fhir:v "GenomicStudyMethodTypeCS"] ; # 
  fhir:title [ fhir:v "Genomic Study Method Type CodeSystem"] ; # 
  fhir:status [ fhir:v "active"] ; # 
  fhir:experimental [ fhir:v "true"^^xsd:boolean] ; # 
  fhir:date [ fhir:v "2024-04-09T13:57:55+00:00"^^xsd:dateTime] ; # 
  fhir:publisher [ fhir:v "HL7 International / Clinical Genomics"] ; # 
  fhir:contact ( [
fhir:name [ fhir:v "HL7 International / Clinical Genomics" ] ;
    ( fhir:telecom [
fhir:system [ fhir:v "url" ] ;
fhir:value [ fhir:v "http://www.hl7.org/Special/committees/clingenomics" ]     ] [
fhir:system [ fhir:v "email" ] ;
fhir:value [ fhir:v "cg@lists.HL7.org" ]     ] )
  ] ) ; # 
  fhir:description [ fhir:v "Backport of http://hl7.org/fhir/genomicstudy-methodtype"] ; # 
  fhir:jurisdiction ( [
    ( fhir:coding [
fhir:system [ fhir:v "http://unstats.un.org/unsd/methods/m49/m49.htm"^^xsd:anyURI ] ;
fhir:code [ fhir:v "001" ] ;
fhir:display [ fhir:v "World" ]     ] )
  ] ) ; # 
  fhir:caseSensitive [ fhir:v "true"^^xsd:boolean] ; # 
  fhir:content [ fhir:v "complete"] ; # 
  fhir:count [ fhir:v "81"^^xsd:nonNegativeInteger] ; # 
  fhir:concept ( [
fhir:code [ fhir:v "biochemical-genetics" ] ;
fhir:display [ fhir:v "Biochemical Genetics" ]
  ] [
fhir:code [ fhir:v "cytogenetics" ] ;
fhir:display [ fhir:v "Cytogenetics" ]
  ] [
fhir:code [ fhir:v "molecular-genetics" ] ;
fhir:display [ fhir:v "Molecular Genetics" ]
  ] [
fhir:code [ fhir:v "analyte" ] ;
fhir:display [ fhir:v "Analyte" ]
  ] [
fhir:code [ fhir:v "chromosome-breakage-studies" ] ;
fhir:display [ fhir:v "Chromosome breakage studies" ]
  ] [
fhir:code [ fhir:v "deletion-duplication-analysis" ] ;
fhir:display [ fhir:v "Deletion/duplication analysis" ]
  ] [
fhir:code [ fhir:v "detection-of-homozygosity" ] ;
fhir:display [ fhir:v "Detection of homozygosity" ]
  ] [
fhir:code [ fhir:v "enzyme-assay" ] ;
fhir:display [ fhir:v "Enzyme assay" ]
  ] [
fhir:code [ fhir:v "fish-interphase" ] ;
fhir:display [ fhir:v "FISH-interphase" ]
  ] [
fhir:code [ fhir:v "fish-metaphase" ] ;
fhir:display [ fhir:v "FISH-metaphase" ]
  ] [
fhir:code [ fhir:v "flow-cytometry" ] ;
fhir:display [ fhir:v "Flow cytometry" ]
  ] [
fhir:code [ fhir:v "fish" ] ;
fhir:display [ fhir:v "Fluorescence in situ hybridization (FISH)" ]
  ] [
fhir:code [ fhir:v "immunohistochemistry" ] ;
fhir:display [ fhir:v "Immunohistochemistry" ]
  ] [
fhir:code [ fhir:v "karyotyping" ] ;
fhir:display [ fhir:v "Karyotyping" ]
  ] [
fhir:code [ fhir:v "linkage-analysis" ] ;
fhir:display [ fhir:v "Linkage analysis" ]
  ] [
fhir:code [ fhir:v "methylation-analysis" ] ;
fhir:display [ fhir:v "Methylation analysis" ]
  ] [
fhir:code [ fhir:v "msi" ] ;
fhir:display [ fhir:v "Microsatellite instability testing (MSI)" ]
  ] [
fhir:code [ fhir:v "m-fish" ] ;
fhir:display [ fhir:v "Multicolor FISH (M-FISH)" ]
  ] [
fhir:code [ fhir:v "mutation-scanning-of-select-exons" ] ;
fhir:display [ fhir:v "Mutation scanning of select exons" ]
  ] [
fhir:code [ fhir:v "mutation-scanning-of-the-entire-coding-region" ] ;
fhir:display [ fhir:v "Mutation scanning of the entire coding region" ]
  ] [
fhir:code [ fhir:v "protein-analysis" ] ;
fhir:display [ fhir:v "Protein analysis" ]
  ] [
fhir:code [ fhir:v "protein-expression" ] ;
fhir:display [ fhir:v "Protein expression" ]
  ] [
fhir:code [ fhir:v "rna-analysis" ] ;
fhir:display [ fhir:v "RNA analysis" ]
  ] [
fhir:code [ fhir:v "sequence-analysis-of-select-exons" ] ;
fhir:display [ fhir:v "Sequence analysis of select exons" ]
  ] [
fhir:code [ fhir:v "sequence-analysis-of-the-entire-coding-region" ] ;
fhir:display [ fhir:v "Sequence analysis of the entire coding region" ]
  ] [
fhir:code [ fhir:v "sister-chromatid-exchange" ] ;
fhir:display [ fhir:v "Sister chromatid exchange" ]
  ] [
fhir:code [ fhir:v "targeted-variant-analysis" ] ;
fhir:display [ fhir:v "Targeted variant analysis" ]
  ] [
fhir:code [ fhir:v "udp" ] ;
fhir:display [ fhir:v "Uniparental disomy study (UPD)" ]
  ] [
fhir:code [ fhir:v "aspe" ] ;
fhir:display [ fhir:v "Allele-specific primer extension (ASPE)" ]
  ] [
fhir:code [ fhir:v "alternative-splicing-detection" ] ;
fhir:display [ fhir:v "Alternative splicing detection" ]
  ] [
fhir:code [ fhir:v "bi-directional-sanger-sequence-analysis" ] ;
fhir:display [ fhir:v "Bi-directional Sanger Sequence Analysis" ]
  ] [
fhir:code [ fhir:v "c-banding" ] ;
fhir:display [ fhir:v "C-banding" ]
  ] [
fhir:code [ fhir:v "cia" ] ;
fhir:display [ fhir:v "Chemiluminescent Immunoassay (CIA)" ]
  ] [
fhir:code [ fhir:v "chromatin-immunoprecipitation-on-chip" ] ;
fhir:display [ fhir:v "Chromatin Immunoprecipitation on ChIP" ]
  ] [
fhir:code [ fhir:v "comparative-genomic-hybridization" ] ;
fhir:display [ fhir:v "Comparative Genomic Hybridization" ]
  ] [
fhir:code [ fhir:v "damid" ] ;
fhir:display [ fhir:v "DamID" ]
  ] [
fhir:code [ fhir:v "digital-virtual-karyotyping" ] ;
fhir:display [ fhir:v "Digital / Virtual karyotyping" ]
  ] [
fhir:code [ fhir:v "digital-microfluidic-microspheres" ] ;
fhir:display [ fhir:v "Digital microfluidic microspheres" ]
  ] [
fhir:code [ fhir:v "enzymatic-levels" ] ;
fhir:display [ fhir:v "Enzymatic levels" ]
  ] [
fhir:code [ fhir:v "enzyme-activity" ] ;
fhir:display [ fhir:v "Enzyme activity" ]
  ] [
fhir:code [ fhir:v "elisa" ] ;
fhir:display [ fhir:v "Enzyme-Linked Immunosorbent Assays (ELISA)" ]
  ] [
fhir:code [ fhir:v "fluorometry" ] ;
fhir:display [ fhir:v "Fluorometry" ]
  ] [
fhir:code [ fhir:v "fusion-genes-microarrays" ] ;
fhir:display [ fhir:v "Fusion genes microarrays" ]
  ] [
fhir:code [ fhir:v "g-banding" ] ;
fhir:display [ fhir:v "G-banding" ]
  ] [
fhir:code [ fhir:v "gc-ms" ] ;
fhir:display [ fhir:v "Gas chromatographymass spectrometry (GC-MS)" ]
  ] [
fhir:code [ fhir:v "gene-expression-profiling" ] ;
fhir:display [ fhir:v "Gene expression profiling" ]
  ] [
fhir:code [ fhir:v "gene-id" ] ;
fhir:display [ fhir:v "GeneID" ]
  ] [
fhir:code [ fhir:v "gold-nanoparticle-probe-technology" ] ;
fhir:display [ fhir:v "Gold nanoparticle probe technology" ]
  ] [
fhir:code [ fhir:v "hplc" ] ;
fhir:display [ fhir:v "High-performance liquid chromatography (HPLC)" ]
  ] [
fhir:code [ fhir:v "lc-ms" ] ;
fhir:display [ fhir:v "Liquid chromatography mass spectrometry (LC-MS)" ]
  ] [
fhir:code [ fhir:v "lc-ms-ms" ] ;
fhir:display [ fhir:v "Liquid chromatography-tandem mass spectrometry (LC-MS/MS)" ]
  ] [
fhir:code [ fhir:v "metabolite-levels" ] ;
fhir:display [ fhir:v "Metabolite levels" ]
  ] [
fhir:code [ fhir:v "methylation-specific-pcr" ] ;
fhir:display [ fhir:v "Methylation-specific PCR" ]
  ] [
fhir:code [ fhir:v "microarray" ] ;
fhir:display [ fhir:v "Microarray" ]
  ] [
fhir:code [ fhir:v "mlpa" ] ;
fhir:display [ fhir:v "Multiplex Ligation-dependent Probe Amplification (MLPA)" ]
  ] [
fhir:code [ fhir:v "ngs-mps" ] ;
fhir:display [ fhir:v "Next-Generation (NGS)/Massively parallel sequencing (MPS)" ]
  ] [
fhir:code [ fhir:v "ola" ] ;
fhir:display [ fhir:v "Oligonucleotide Ligation Assay (OLA)" ]
  ] [
fhir:code [ fhir:v "oligonucleotide-hybridization-based-dna-sequencing" ] ;
fhir:display [ fhir:v "Oligonucleotide hybridization-based DNA sequencing" ]
  ] [
fhir:code [ fhir:v "other" ] ;
fhir:display [ fhir:v "Other" ]
  ] [
fhir:code [ fhir:v "pcr" ] ;
fhir:display [ fhir:v "PCR" ]
  ] [
fhir:code [ fhir:v "pcr-with-allele-specific-hybridization" ] ;
fhir:display [ fhir:v "PCR with allele specific hybridization" ]
  ] [
fhir:code [ fhir:v "pcr-rflp-with-southern-hybridization" ] ;
fhir:display [ fhir:v "PCR-RFLP with Southern hybridization" ]
  ] [
fhir:code [ fhir:v "protein-truncation-test" ] ;
fhir:display [ fhir:v "Protein truncation test" ]
  ] [
fhir:code [ fhir:v "pyrosequencing" ] ;
fhir:display [ fhir:v "Pyrosequencing" ]
  ] [
fhir:code [ fhir:v "q-banding" ] ;
fhir:display [ fhir:v "Q-banding" ]
  ] [
fhir:code [ fhir:v "qpcr" ] ;
fhir:display [ fhir:v "Quantitative PCR (qPCR)" ]
  ] [
fhir:code [ fhir:v "r-banding" ] ;
fhir:display [ fhir:v "R-banding" ]
  ] [
fhir:code [ fhir:v "rflp" ] ;
fhir:display [ fhir:v "RFLP" ]
  ] [
fhir:code [ fhir:v "rt-lamp" ] ;
fhir:display [ fhir:v "RT-LAMP" ]
  ] [
fhir:code [ fhir:v "rt-pcr" ] ;
fhir:display [ fhir:v "RT-PCR" ]
  ] [
fhir:code [ fhir:v "rt-pcr-with-gel-analysis" ] ;
fhir:display [ fhir:v "RT-PCR with gel analysis" ]
  ] [
fhir:code [ fhir:v "rt-qpcr" ] ;
fhir:display [ fhir:v "RT-qPCR" ]
  ] [
fhir:code [ fhir:v "snp-detection" ] ;
fhir:display [ fhir:v "SNP Detection" ]
  ] [
fhir:code [ fhir:v "silver-staining" ] ;
fhir:display [ fhir:v "Silver staining" ]
  ] [
fhir:code [ fhir:v "sky" ] ;
fhir:display [ fhir:v "Spectral karyotyping (SKY)" ]
  ] [
fhir:code [ fhir:v "t-banding" ] ;
fhir:display [ fhir:v "T-banding" ]
  ] [
fhir:code [ fhir:v "ms-ms" ] ;
fhir:display [ fhir:v "Tandem mass spectrometry (MS/MS)" ]
  ] [
fhir:code [ fhir:v "tetra-nucleotide-repeat-by-pcr-or-southern-blot" ] ;
fhir:display [ fhir:v "Tetra-nucleotide repeat by PCR or Southern Blot" ]
  ] [
fhir:code [ fhir:v "tiling-arrays" ] ;
fhir:display [ fhir:v "Tiling Arrays" ]
  ] [
fhir:code [ fhir:v "trinucleotide-repeat-by-pcr-or-southern-blot" ] ;
fhir:display [ fhir:v "Trinucleotide repeat by PCR or Southern Blot" ]
  ] [
fhir:code [ fhir:v "uni-directional-sanger-sequencing" ] ;
fhir:display [ fhir:v "Uni-directional Sanger sequencing" ]
  ] ) . #