Comparative Genomic Hybridization
"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 |
|---|
| 2010 | 1 | 0 | 1 |
| 2011 | 3 | 0 | 3 |
| 2012 | 1 | 1 | 2 |
| 2013 | 0 | 2 | 2 |
| 2014 | 0 | 1 | 1 |
| 2015 | 0 | 5 | 5 |
| 2016 | 0 | 2 | 2 |
| 2017 | 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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A novel TLX1-driven T-ALL zebrafish model: comparative genomic analysis with other leukemia models. Leukemia. 2020 12; 34(12):3398-3403.
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Giant Cell Ependymoma of Lateral Ventricle: Case Report, Literature Review, and Analysis of Prognostic Factors and Genetic Profile. World Neurosurg. 2017 Dec; 108:997.e9-997.e14.
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Genomic characterization of recurrent high-grade astroblastoma. Cancer Genet. 2016 Jul-Aug; 209(7-8):321-30.
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Oncogenic PI3K mutations are as common as AKT1 and SMO mutations in meningioma. Neuro Oncol. 2016 05; 18(5):649-55.
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Chromosomal copy number alterations and HPV integration in cervical precancer and invasive cancer. Carcinogenesis. 2016 Feb; 37(2):188-196.
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A prognostic cytogenetic scoring system to guide the adjuvant management of patients with atypical meningioma. Neuro Oncol. 2016 Feb; 18(2):269-74.
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Acquired genetic alterations in tumor cells dictate the development of high-risk neuroblastoma and clinical outcomes. BMC Cancer. 2015 Jul 10; 15:514.
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Characterization of cells from patient-derived fibrovascular membranes in proliferative diabetic retinopathy. Mol Vis. 2015; 21:673-87.
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Clinical implementation of integrated whole-genome copy number and mutation profiling for glioblastoma. Neuro Oncol. 2015 Oct; 17(10):1344-55.
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Angiomatous meningiomas have a distinct genetic profile with multiple chromosomal polysomies including polysomy of chromosome 5. Oncotarget. 2014 Nov 15; 5(21):10596-606.