"Comparative Genomic Hybridization" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A method for comparing two sets of chromosomal DNA by analyzing differences in the copy number and location of specific sequences. It is used to look for large sequence changes such as deletions, duplications, amplifications, or translocations.
| Descriptor ID |
D055028
|
| MeSH Number(s) |
E05.393.285.240 E05.393.520.500 E05.393.661.187
|
| Concept/Terms |
Comparative Genomic Hybridization- Comparative Genomic Hybridization
- Comparative Genomic Hybridizations
- Genomic Hybridization, Comparative
- Genomic Hybridizations, Comparative
- Hybridization, Comparative Genomic
- Hybridizations, Comparative Genomic
- Comparative Genome Hybridization
- Comparative Genome Hybridizations
- Genome Hybridization, Comparative
- Genome Hybridizations, Comparative
- Hybridization, Comparative Genome
- Hybridizations, Comparative Genome
|
Below are MeSH descriptors whose meaning is more general than "Comparative Genomic Hybridization".
Below are MeSH descriptors whose meaning is more specific than "Comparative Genomic Hybridization".
This graph shows the total number of publications written about "Comparative Genomic Hybridization" by people in this website by year, and whether "Comparative Genomic Hybridization" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2009 | 0 | 1 | 1 |
| 2010 | 0 | 1 | 1 |
| 2011 | 0 | 2 | 2 |
| 2012 | 0 | 1 | 1 |
| 2013 | 0 | 2 | 2 |
| 2014 | 1 | 3 | 4 |
| 2015 | 0 | 2 | 2 |
| 2016 | 0 | 3 | 3 |
| 2017 | 0 | 1 | 1 |
| 2018 | 0 | 2 | 2 |
| 2019 | 0 | 1 | 1 |
| 2020 | 0 | 1 | 1 |
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Below are the most recent publications written about "Comparative Genomic Hybridization" by people in Profiles.
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Morpho-functional survey in children suspected of inherited retinal dystrophies via video recording, electrophysiology and genetic analysis. Int Ophthalmol. 2020 Oct; 40(10):2523-2534.
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Distinctive mutational spectrum and karyotype disruption in long-term cisplatin-treated urothelial carcinoma cell lines. Sci Rep. 2019 10 09; 9(1):14476.
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LRBA Deficiency in a Patient With a Novel Homozygous Mutation Due to Chromosome 4 Segmental Uniparental Isodisomy. Front Immunol. 2018; 9:2397.
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Rare gene deletions in genetic generalized and Rolandic epilepsies. PLoS One. 2018; 13(8):e0202022.
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Genomewide association study on monoclonal gammopathy of unknown significance (MGUS). Eur J Haematol. 2017 Jul; 99(1):70-79.
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De novo microdeletions and point mutations affecting SOX2 in three individuals with intellectual disability but without major eye malformations. Am J Med Genet A. 2017 Feb; 173(2):435-443.
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Genetic Analysis of 'PAX6-Negative' Individuals with Aniridia or Gillespie Syndrome. PLoS One. 2016; 11(4):e0153757.
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Generation of human induced pluripotent stem cell line from a patient with a long QT syndrome type 2. Stem Cell Res. 2016 Mar; 16(2):304-7.
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EpCAM-Independent Enrichment of Circulating Tumor Cells in Metastatic Breast Cancer. PLoS One. 2015; 10(12):e0144535.
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Mutational dynamics between primary and relapse neuroblastomas. Nat Genet. 2015 Aug; 47(8):872-7.
MeSH information
