SeeGH – A software tool for visualization of whole genome array comparative genomic hybridization data

BACKGROUND: Array comparative genomic hybridization (CGH) is a technique which detects copy number differences in DNA segments. Complete sequencing of the human genome and the development of an array representing a tiling set of tens of thousands of DNA segments spanning the entire human genome has...

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Detalles Bibliográficos
Autores principales: Chi, Bryan, deLeeuw, Ronald J, Coe, Bradley P, MacAulay, Calum, Lam, Wan L
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2004
Materias:
Software
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC373529/
https://www.ncbi.nlm.nih.gov/pubmed/15040819
http://dx.doi.org/10.1186/1471-2105-5-13

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC373529/
https://www.ncbi.nlm.nih.gov/pubmed/15040819
http://dx.doi.org/10.1186/1471-2105-5-13

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