101397-8
Copy number variation analysis in Blood or Tissue 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
LOINC Names Get Info
- Fully-Specified Name
- Copy number variation analysis:
Find: Pt: Bld/Tiss: Doc: Sequencing - Long Common Name
- Copy number variation analysis in Blood or Tissue by Sequencing
- Short Name
- CNV analysis Bld/T Seq
- Display Name
- Copy number variation analysis Sequencing Doc (Bld/Tiss)
- Consumer Name Alpha Get Info
- Copy number variation analysis, Blood or tissue specimen
Part Model Get Info
- Component
- Copy number variation analysis
LP433611-3
- Analyte
- Copy number variation analysis
LP433611-3
- Component Numerator
- Copy number variation analysis
LP433611-3
- Component Numerator Core
- Copy number variation analysis
LP433611-3
- Component Numerator Core Suffix
- NULL
- Component Denominator
- NULL
- Component Denominator Core
- NULL
- Component Denominator Core Suffix
- NULL
- Challenge
- NULL
- Adjustment
- NULL
- Count
- NULL
- Property
- Find
LP6813-2
- Time
- Pt
LP6960-1
- Time Core
- Pt
LP6960-1
- Time Modifier
- NULL
- System
- Bld/Tiss
LP7061-7
- System Core
- Bld/Tiss
LP7061-7
- Super System
- NULL
- Scale
- Doc
LP32888-7
- Method
- Sequencing
LP150045-5
Basic Attributes
- Class
- MOLPATH
- Type
- Laboratory
- First Released
- Version 2.74
- Last Updated
- Version 2.75 (MIN)
- Order vs. Observation
- Both
Language Variants Get Info
| Tag | Language | Translation |
|---|---|---|
| ar-JO | Arabic (Jordan) | فحص تباين عدد النسخ في الدم أو الأنسجة ( بتقنية التسلسل ) |
| cs-CZ | Czech (Czechia) | Variabilita počtu kopií (CNV) analýza: |
| el-GR | Greek (Greece) | Ανάλυση διακύμανσης αριθμού αντιγράφων: Synonyms: Doc MOLPATH Pt Αίμα Αίμα/Ιστός Αλληλούχιση Ανάλυση διακύμανσης αριθμού αντιγράφων Αριθμός Εύρεση Ιστός |
| es-ES | Spanish (Spain) | Análisis de variación del número de copias: |
| fr-FR | French (France) | Variation du nombre de copies: |
| it-IT | Italian (Italy) | Analisi della variazione del numero copie: Synonyms: Osservazione Patologia molecolare Punto nel tempo (episodio) Sangue Sangue o Tessuto Tessuto & |
| nl-NL | Dutch (Netherlands) | variatie in aantal kopieën analyse: |
| pl-PL | Polish (Poland) | Analiza zmienności liczby kopii: |
| zh-CN | Chinese (China) | 拷贝数变异分析: Synonyms: 个数; |
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.
LOINC Copyright
Copyright © Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. See https://