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
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| 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 |
|---|
| 2011 | 1 | 2 | 3 |
| 2012 | 2 | 0 | 2 |
| 2014 | 1 | 0 | 1 |
| 2016 | 0 | 2 | 2 |
| 2017 | 1 | 10 | 11 |
| 2018 | 0 | 8 | 8 |
| 2019 | 1 | 4 | 5 |
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Below are the most recent publications written about "Comparative Genomic Hybridization" by people in Profiles.
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Genomic investigation of Staphylococcus aureus recovered from Gambian women and newborns following an oral dose of intra-partum azithromycin. J Antimicrob Chemother. 2019 11 01; 74(11):3170-3178.
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Actionable molecular alterations in advanced gynaecologic malignancies: updated results from the ProfiLER programme. Eur J Cancer. 2019 09; 118:156-165.
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Characterization of HCC Mouse Models: Towards an Etiology-Oriented Subtyping Approach. Mol Cancer Res. 2019 07; 17(7):1493-1502.
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Comparative genomic analysis unravels the transmission pattern and intra-species divergence of acute hepatopancreatic necrosis disease (AHPND)-causing Vibrio parahaemolyticus strains. Mol Genet Genomics. 2019 Aug; 294(4):1007-1022.
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Advantages of Array Comparative Genomic Hybridization Using Buccal Swab DNA for Detecting Pallister-Killian Syndrome. Ann Lab Med. 2019 Mar; 39(2):232-234.
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Genomic changes of chromosomes 8p23.1 and 1q21: Novel mutations in malignant mesothelioma. Lung Cancer. 2018 12; 126:106-111.
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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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Added Value of Whole-Exome and Transcriptome Sequencing for Clinical Molecular Screenings of Advanced Cancer Patients With Solid Tumors. Cancer J. 2018 Jul/Aug; 24(4):153-162.
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Combinational chromosomal aneuploidies and HPV status for prediction of head and neck squamous cell carcinoma prognosis in biopsies and cytological preparations. J Cancer Res Clin Oncol. 2018 Jun; 144(6):1129-1141.
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TNFAIP3 haploinsufficiency is the cause of autoinflammatory manifestations in a patient with a deletion of 13Mb on chromosome 6. Clin Immunol. 2018 06; 191:44-51.