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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, potentially across many samples, is an important process in the identification and analysis of SVs.
(Almagro-Garcia et al., 2009) SnoopCGH: software for visualizing comparative genomic hybridization data. Bioinformatics.