SnoopCGH: software for visualizing comparative genomic hybridization data

Summary: Array-based comparative genomic hybridization (CGH) technology is used to discover and validate genomic structural variation, including copy number variants, insertions, deletions and other structural variants (SVs). The visualization and summarization of the array CGH data outputs, potenti...

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Detalhes bibliográficos
Main Authors: Almagro-Garcia, Jacob, Manske, Magnus, Carret, Celine, Campino, Susana, Auburn, Sarah, MacInnis, Bronwyn L, Maslen, Gareth, Pain, Arnab, Newbold, Christopher I, Kwiatkowski, Dominic P, Clark, Taane G
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2009
Assuntos:
Applications Note
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2759554/
https://ncbi.nlm.nih.gov/pubmed/19687029
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btp488
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