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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Bibliographic Details
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
Format: Artigo
Language:Inglês
Published: Oxford University Press 2009
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Applications Note
Online Access: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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