103736-5
Erythrocytosis focused multigene analysis in Specimen by Sequencing
Active
Part Description
LP150045-5 Sequencing
Sequencing is a method used to determine the sequence of individual genes, larger genetic regions (i.e. clusters of genes or operons), full chromosomes or entire genomes. Historically, most sequencing has been performed using the chain termination method developed by Frederick Sanger in 1977. PMID: 271968 Sequencing technologies have improved dramatically, making them cheaper, faster, and more accurate. Next-generation sequencing (NGS), also known as high-throughput sequencing, deep sequencing, and second-generation sequencing, is a type of technology that uses parallel sequencing of multiple small fragments of DNA to determine sequence. This "high-throughput" technology has increased the speed and amount of DNA sequenced at a significantly reduced cost. PMID: 18576944 Several NGS platforms (ie, sequencing instruments and associated reagents) have been developed. Third-generation sequencing is another methodology currently under development that uses parallel sequencing similar to NGS. In contrast to NGS, third-generation sequencing uses single DNA molecules rather than amplified DNA as a template. PMID: 20858600
Source: Regenstrief LOINC
Fully-Specified Name
- Component
- Erythrocytosis focused multigene analysis
- Property
- Find
- Time
- Pt
- System
- XXX
- Scale
- Doc
- Method
- Sequencing
Additional Names
- Short Name
- Erythrocytosis focus multi Spec Seq
- Display Name
- Erythrocytosis focused multigene analysis Sequencing Doc (Specimen)
- Consumer Name Alpha Get Info
- Erythrocytosis focused multigene analysis, Specimen
Basic Attributes
- Class
- MOLPATH
- Type
- Laboratory
- First Released
- Version 2.77
- Last Updated
- Version 2.77
- Order vs. Observation
- Both
Language Variants Get Info
Tag | Language | Translation |
---|---|---|
es-ES | Spanish (Spain) | Análisis multigénico centrado en la eritrocitosis.: |
it-IT | Italian (Italy) | Analisi multigenica focalizzata sull'eritrocitosi: Synonyms: Osservazione Patologia molecolare Punto nel tempo (episodio) |
nl-NL | Dutch (Netherlands) | multigen-analyse gericht op polycytemie: |
LOINC Terminology Service (API) using HL7® FHIR® Get Info
Requests to this service require a free LOINC username and password. Below is a sample of the possible capabilities. See the LOINC Terminology Service documentation for more information.
- CodeSystem lookup
- https:
//fhir.loinc.org/CodeSystem/$lookup?system=http: //loinc.org&code=103736-5
LOINC Copyright
Copyright © 2024 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright