77021-4
Fetal Y chromosome [Presence] based on Plasma cell-free DNA 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
- Fetal Y chromosome:
PrThr: Pt: Plas.cfDNA: Ord: Sequencing - Long Common Name
- Fetal Y chromosome [Presence] based on Plasma cell-free DNA by Sequencing
- Short Name
- Fet Y Chrom Plas.cfDNA Ql
- Display Name
- Y chromosome Sequencing Ql (cfDNA)
- Consumer Name Alpha Get Info
- Fetal Y chromosome
Part Model Get Info
- Component
- Fetal Y chromosome
LP410747-2
- Analyte
- Fetal Y chromosome
LP410747-2
- Component Numerator
- Fetal Y chromosome
LP410747-2
- Component Numerator Core
- Fetal Y chromosome
LP410747-2
- Component Numerator Core Suffix
- NULL
- Component Denominator
- NULL
- Component Denominator Core
- NULL
- Component Denominator Core Suffix
- NULL
- Challenge
- NULL
- Adjustment
- NULL
- Count
- NULL
- Property
- PrThr
LP217195-9
- Time
- Pt
LP6960-1
- Time Core
- Pt
LP6960-1
- Time Modifier
- NULL
- System
- Plas.cfDNA
LP185795-4
- System Core
- Plas.cfDNA
LP185795-4
- Super System
- NULL
- Scale
- Ord
LP7751-3
- Method
- Sequencing
LP150045-5
Example Answer List: LL744-4
Source: Regenstrief Institute| Answer | Code | Score | Answer ID |
|---|---|---|---|
| Detected | LA11882-0 | ||
| Not detected | LA11883-8 |
Basic Attributes
- Class
- MOLPATH
- Type
- Laboratory
- First Released
- Version 2.52
- Last Updated
- Version 2.73 (MIN)
- Change Reason
- The PrThr property is used for LOINC terms whose results are reported using an ordered categorical scale, regardless of whether or not an internal threshold was used to make that determination. This change was approved by the Laboratory LOINC Committee in June 2016.; Added "Fetal" to Component to clarify that the result is about the fetus.
- Order vs. Observation
- Observation
- Common Test Rank Get Info
- 7336
Member of these Panels
| LOINC | Long Common Name |
|---|---|
| 77018-0 | Noninvasive prenatal fetal 13 and 18 and 21 aneuploidy panel - Plasma cell-free DNA by Sequencing |
| 92901-8 | Noninvasive prenatal fetal aneuploidy and microdeletion panel - Plasma cell-free DNA by Sequencing |
Language Variants Get Info
| Tag | Language | Translation |
|---|---|---|
| cs-CZ | Czech (Czechia) | Chromozom Y plodu: |
| el-GR | Greek (Greece) | Εμβρυικό χρωμόσωμα Y: Synonyms: MOLPATH Ord PrThr Pt Αλληλούχιση Εμβρυικό χρωμόσωμα Y Πλάσμα Πλάσμα.cfDNA Χρωμόσωμα Χρωμόσωμα Υ |
| es-ES | Spanish (Spain) | Cromosoma fetal Y: |
| es-MX | Spanish (Mexico) | Cromosoma Y fetal: |
| fr-FR | French (France) | Chromosome foetal Y: |
| it-IT | Italian (Italy) | Cromosoma Y: Synonyms: Cromosoma Y DNA libero circolante nel plasma Patologia molecolare Plasma Presenza o Soglia Punto nel tempo (episodio) |
| nl-NL | Dutch (Netherlands) | foetaal Y-chromosoom: Synonyms: circulerend DNA |
| pl-PL | Polish (Poland) | Chromosom Y płodu: Synonyms: Chromosom Y u płodu wolnokrążące DNA w osoczu |
| zh-CN | Chinese (China) | 胎儿染色体 Y: Synonyms: 依次型; |
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://