| Package | rki.demis.igs |
| Resource Type | CodeSystem |
| Id | sequencingStrategy |
| FHIR Version | R4 |
| Source | https://demis.rki.de/fhir/igs/https://simplifier.net/resolve?scope=rki.demis.igs@3.0.0&canonical=https://demis.rki.de/fhir/igs/CodeSystem/sequencingStrategy |
| URL | https://demis.rki.de/fhir/igs/CodeSystem/sequencingStrategy |
| Version | 2.0.0 |
| Status | active |
| Date | 2024-07-24 |
| Name | SequencingStrategy |
| Title | Sequenzierungsstrategie |
| Description | Das CodeSystem SequencingStrategy enthält die Codes der Sequenzierungsstrategien (angelehnt an ENA). |
| Content | complete |
| ValueSet | |
| sequencingStrategy | Sequenzierungsstrategie |
No resources found
No narrative content found in resource
{
"resourceType": "CodeSystem",
"id": "sequencingStrategy",
"url": "https://demis.rki.de/fhir/igs/CodeSystem/sequencingStrategy",
"version": "2.0.0",
"name": "SequencingStrategy",
"title": "Sequenzierungsstrategie",
"status": "active",
"experimental": false,
"date": "2024-07-24",
"publisher": "Robert Koch-Institut",
"description": "Das CodeSystem SequencingStrategy enthält die Codes der Sequenzierungsstrategien (angelehnt an ENA).",
"caseSensitive": false,
"valueSet": "https://demis.rki.de/fhir/igs/ValueSet/sequencingStrategy",
"content": "complete",
"count": 36,
"concept": [
{
"code": "wgs",
"display": "Whole Genome Sequencing - random sequencing of the whole genome (see pubmed 10731132 for details)"
},
{
"code": "wga",
"display": "Whole Genome Amplification followed by random sequencing. (see pubmed 1631067,8962113 for details)"
},
{
"code": "wxs",
"display": "Random sequencing of exonic regions selected from the genome. (see pubmed 20111037 for details)"
},
{
"code": "rna-seq",
"display": "Random sequencing of whole transcriptome, also known as Whole Transcriptome Shotgun Sequencing, or WTSS). (see pubmed 18611170 for details)"
},
{
"code": "ssrna-seq",
"display": "Strand-specific RNA sequencing."
},
{
"code": "mirna-seq",
"display": "Micro RNA sequencing strategy designed to capture post-transcriptional RNA elements and include non-coding functional elements. (see pubmed 21787409 for details)"
},
{
"code": "ncrna-seq",
"display": "Capture of other non-coding RNA types, including post-translation modification types such as snRNA (small nuclear RNA) or snoRNA (small nucleolar RNA), or expression regulation types such as siRNA (small interfering RNA) or piRNA/piwi/RNA (piwi-interacting RNA)."
},
{
"code": "fl-cdna",
"display": "Full-length sequencing of cDNA templates"
},
{
"code": "est",
"display": "Single pass sequencing of cDNA templates"
},
{
"code": "hi-c",
"display": "Chromosome Conformation Capture technique where a biotin-labeled nucleotide is incorporated at the ligation junction, enabling selective purification of chimeric DNA ligation junctions followed by deep sequencing."
},
{
"code": "atac-seq",
"display": "Assay for Transposase-Accessible Chromatin (ATAC) strategy is used to study genome-wide chromatin accessibility. alternative method to DNase-seq that uses an engineered Tn5 transposase to cleave DNA and to integrate primer DNA sequences into the cleaved genomic DNA."
},
{
"code": "wcs",
"display": "Random sequencing of a whole chromosome or other replicon isolated from a genome."
},
{
"code": "rad-seq",
"display": "RAD sequencing"
},
{
"code": "clone",
"display": "Genomic clone based (hierarchical) sequencing."
},
{
"code": "poolclone",
"display": "Shotgun of pooled clones (usually BACs and Fosmids)."
},
{
"code": "amplicon",
"display": "Sequencing of overlapping or distinct PCR or RT-PCR products. For example, metagenomic community profiling using SSU rRNA."
},
{
"code": "cloneend",
"display": "Clone end (5’, 3’, or both) sequencing."
},
{
"code": "finishing",
"display": "Sequencing intended to finish (close) gaps in existing coverage."
},
{
"code": "chip-seq",
"display": "ChIP-seq, Chromatin ImmunoPrecipitation, reveals binding sites of specific proteins, typically transcription factors (TFs) using antibodies to extract DNA fragments bound to the target protein."
},
{
"code": "mnase-seq",
"display": "Identifies well-positioned nucleosomes. uses Micrococcal Nuclease (MNase) is an endo-exonuclease that processively digests DNA until an obstruction, such as a nucleosome, is reached."
},
{
"code": "dnase-hypersensitivity",
"display": "Sequencing of hypersensitive sites, or segments of open chromatin that are more readily cleaved by DNaseI."
},
{
"code": "bisulfite-seq",
"display": "MethylC-seq. Sequencing following treatment of DNA with bisulfite to convert cytosine residues to uracil depending on methylation status."
},
{
"code": "cts",
"display": "Concatenated Tag Sequencing"
},
{
"code": "mre-seq",
"display": "Methylation-Sensitive Restriction Enzyme Sequencing."
},
{
"code": "medip-seq",
"display": "Methylated DNA Immunoprecipitation Sequencing."
},
{
"code": "mbd-seq",
"display": "Methyl CpG Binding Domain Sequencing."
},
{
"code": "tn-seq",
"display": "Quantitatively determine fitness of bacterial genes based on how many times a purposely seeded transposon gets inserted into each gene of a colony after some time."
},
{
"code": "validation",
"display": "CGHub special request"
},
{
"code": "faire-seq",
"display": "Formaldehyde Assisted Isolation of Regulatory Elements. Reveals regions of open chromatin."
},
{
"code": "selex",
"display": "Systematic Evolution of Ligands by Exponential enrichment"
},
{
"code": "rip-seq",
"display": "Direct sequencing of RNA immunoprecipitates (includes CLIP-Seq, HITS-CLIP and PAR-CLIP)."
},
{
"code": "chia-pet",
"display": "Direct sequencing of proximity-ligated chromatin immunoprecipitates."
},
{
"code": "synthetic-long-read",
"display": "binning and barcoding of large DNA fragments to facilitate assembly of the fragment"
},
{
"code": "targeted-capture",
"display": "Enrichment of a targeted subset of loci."
},
{
"code": "tethered-chromatin-conformation-capture",
"display": "Tethered Chromatin Conformation Capture"
},
{
"code": "other",
"display": "Library strategy not listed."
}
]
}