92902-6Fetal Chromosome region 8q24 deletion [Presence] based on Plasma cell-free DNA by SequencingActive
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
- Fetal chromosome region 8q24 deletion
- Short Name
- Fet Chr 8q24 Del Plas.cfDNA Ql
- Display Name
- Chromosome region 8q24 del Sequencing Ql (cfDNA)
- First Released
- Version 2.66
- Last Updated
- Version 2.66
- Change Reason
- Added "Fetal" to Component to clarify that the result is about the fetus.
- Order vs. Observation
Example Answer List LL360-9
Source: Regenstrief Institute
|Positive Copyright http://snomed.info/sct ID:10828004 Positive (qualifier value)||LA6576-8|
|Negative Copyright http://snomed.info/sct ID:260385009 Negative (qualifier value)||LA6577-6|
Member of these Panels
|LOINC||Long Common Name|
|92901-8||Noninvasive prenatal fetal aneuploidy and microdeletion panel - Plasma cell-free DNA by Sequencing|
Language Variants Get Info
- zh-CNChinese (CHINA)
- 胎儿染色体区域 8q24 缺失:
存在情况或阈值: 时间点: 血浆.cfDNA: 序数型: 序列测定
LOINC FHIR® API Example - CodeSystem Request Get Info
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Copyright © 2019 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright