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.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

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 Array-Based Comparative Genomic Hybridization Array-Based Comparative Genomic Hybridization Array Based Comparative Genomic Hybridization Array Comparative Genomic Hybridization

Below are MeSH descriptors whose meaning is more general than "Comparative Genomic Hybridization".

Analytical, Diagnostic and Therapeutic Techniques and Equipment [E]
Investigative Techniques [E05]
Genetic Techniques [E05.393]
Cytogenetic Analysis [E05.393.285]
Comparative Genomic Hybridization [E05.393.285.240]
Molecular Diagnostic Techniques [E05.393.520]
Comparative Genomic Hybridization [E05.393.520.500]
Nucleic Acid Hybridization [E05.393.661]
Comparative Genomic Hybridization [E05.393.661.187]

Below are MeSH descriptors whose meaning is related to "Comparative Genomic Hybridization".

Below are MeSH descriptors whose meaning is more specific than "Comparative Genomic Hybridization".

publications

Timeline | Most Recent

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.

Bar chart showing 11 publications over 9 distinct years, with a maximum of 3 publications in 2009

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
2008	0	1	1
2009	1	2	3
2010	0	1	1
2011	0	1	1
2012	0	1	1
2013	0	1	1
2014	0	1	1
2015	0	1	1
2016	1	0	1

Below are the most recent publications written about "Comparative Genomic Hybridization" by people in Profiles.

Yoshikawa Y, Emi M, Hashimoto-Tamaoki T, Ohmuraya M, Sato A, Tsujimura T, Hasegawa S, Nakano T, Nasu M, Pastorino S, Szymiczek A, Bononi A, Tanji M, Pagano I, Gaudino G, Napolitano A, Goparaju C, Pass HI, Yang H, Carbone M. High-density array-CGH with targeted NGS unmask multiple noncontiguous minute deletions on chromosome 3p21 in mesothelioma. Proc Natl Acad Sci U S A. 2016 11 22; 113(47):13432-13437.

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Shen Y, Wang Z, Loo LW, Ni Y, Jia W, Fei P, Risch HA, Katsaros D, Yu H. LINC00472 expression is regulated by promoter methylation and associated with disease-free survival in patients with grade 2 breast cancer. Breast Cancer Res Treat. 2015 Dec; 154(3):473-82.

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Brim H, Abu-Asab MS, Nouraie M, Salazar J, Deleo J, Razjouyan H, Mokarram P, Schaffer AA, Naghibhossaini F, Ashktorab H. An integrative CGH, MSI and candidate genes methylation analysis of colorectal tumors. PLoS One. 2014; 9(1):e82185.

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Perche O, Haddad G, Menuet A, Callier P, Marcos M, Briault S, Laudier B. Dysregulation of FOXG1 pathway in a 14q12 microdeletion case. . 2013 Dec; 161A(12):3072-7.

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Brim H, Lee E, Abu-Asab MS, Chaouchi M, Razjouyan H, Namin H, Goel A, Schäffer AA, Ashktorab H. Genomic aberrations in an African American colorectal cancer cohort reveals a MSI-specific profile and chromosome X amplification in male patients. PLoS One. 2012; 7(8):e40392.

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Loo LW, Wang Y, Flynn EM, Lund MJ, Bowles EJ, Buist DS, Liff JM, Flagg EW, Coates RJ, Eley JW, Hsu L, Porter PL. Genome-wide copy number alterations in subtypes of invasive breast cancers in young white and African American women. Breast Cancer Res Treat. 2011 May; 127(1):297-308.

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Costrop LM, Vanakker OO, Van Laer L, Le Saux O, Martin L, Chassaing N, Guerra D, Pasquali-Ronchetti I, Coucke PJ, De Paepe A. Novel deletions causing pseudoxanthoma elasticum underscore the genomic instability of the ABCC6 region. J Hum Genet. 2010 Feb; 55(2):112-7.

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Yu W, Kanaan Y, Bae YK, Baed YK, Gabrielson E. Chromosomal changes in aggressive breast cancers with basal-like features. Cancer Genet Cytogenet. 2009 Aug; 193(1):29-37.

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Gu J, Neary J, Cai H, Moshfeghian A, Rodriguez SA, Lilburn TG, Wang Y. Genomic and systems evolution in Vibrionaceae species. BMC Genomics. 2009 Jul 07; 10 Suppl 1:S11.

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Suárez E, Burguete A, Mclachlan GJ. Microarray data analysis for differential expression: a tutorial. P R Health Sci J. 2009 Jun; 28(2):89-104.

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