94589-9
Hematologic neoplasm chromosome analysis in Blood or Marrow by Mate pair sequencing
Active
Term Description
This term is used for the order & overall chromosome analysis report for identifying hematologic neoplasms in blood or bone marrow specimens by sequencing methods, such as mate pair sequencing. Results may include the overall findings, the result in ISCN format, testing methods, interpretation, recommendations, and references. This is typically second-tier testing when previous cytogenetic studies have detected an acquired chromosome abnormality of unknown significance.
Source: Regenstrief LOINC
Part Descriptions
LP417552-9 Mate pair sequencing
Mate pair sequencing is a next generation, whole genome sequencing test that may be performed in conjunction with or when previous cytogenetic studies are unsuccessful or detect a chromosome abnormality of unknown significance. Mate pair sequencing is used to determine the size, precise breakpoints, genes involved, and any other attribute of the abnormality that is not detectable by other methods. Large DNA fragments (2-5Kb) are sequenced by paired-end sequencing through the use of a modified library preparation. The longer fragments facilitate identifying breakpoint junction locations with lower base coverage. Results provide diagnostic, prognostic, and therapeutic information for patient care. PMID: 29726617 PMID: 24105367
Source: Regenstrief LOINC
LP417552-9 Mate pair sequencing
Mate pair sequencing is a next generation, whole genome sequencing test that may be performed in conjunction with or when previous cytogenetic studies are unsuccessful or detect a chromosome abnormality of unknown significance. Mate pair sequencing is used to determine the size, precise breakpoints, genes involved, and any other attribute of the abnormality that is not detectable by other methods. Large DNA fragments (2-5Kb) are sequenced by paired-end sequencing through the use of a modified library preparation. The longer fragments facilitate identifying breakpoint junction locations with lower base coverage. Results provide diagnostic, prognostic, and therapeutic information for patient care. PMID: 29726617 PMID: 24105367
Source: Regenstrief LOINC
Fully-Specified Name
- Component
- Hematologic neoplasm chromosome analysis
- Property
- Find
- Time
- Pt
- System
- Bld/Bone mar
- Scale
- Doc
- Method
- Mate pair sequencing
Additional Names
- Short Name
- Hematologic chrom analy Bld/Mar MPSeq
- Display Name
- Hematologic neoplasm chromosome analysis Mate pair sequencing Doc (Bld/BM)
- Consumer Name Alpha Get Info
- Hematologic neoplasm chromosome analysis, Blood Or Bone marrow
Basic Attributes
- Class
- MOLPATH
- Type
- Laboratory
- First Released
- Version 2.68
- Last Updated
- Version 2.68
- Order vs. Observation
- Both
Language Variants Get Info
Tag | Language | Translation |
---|---|---|
es-ES | Spanish (Spain) | Análisis de cromosomas de neoplasias hematológicas: |
es-MX | Spanish (Mexico) | Análisis cromosómico de neoplasias hematológicas: |
fr-FR | French (France) | Chromosome analyse néoplasie hématologique: |
it-IT | Italian (Italy) | Analisi cromosomica del neoplasma ematologico: Synonyms: Midollo osseo Osservazione Patologia molecolare Punto nel tempo (episodio) Sangue Sangue o Midollo |
zh-CN | Chinese (China) | 血液肿瘤染色体分析: Synonyms: 临床文档型; |
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