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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Hlavní autoři: 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
Médium: Artigo
Jazyk:Inglês
Vydáno: Oxford University Press 2009
Témata:
Applications Note
On-line přístup: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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