SnoopCGH -- Comparative Genomic Hybridization software

URL:
http://snoopcgh.sourceforge.net/
What you can do:
Visualize and explore comparative genomic hybridization data sets.
Highlights:
  • SnoopCGH is a software tool for structural variants (SV) analysis using data from array CGH technologies, which is also amenable to short-read sequence data.
  • 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.
Keywords:
  • comparative genomic hybridization
  • genomic structural variation
  • copy number variant
  • insertion
  • deletion
  • structural variant
Literature & Tutorials:
PubMed Link: SnoopCGH: software for visualizing comparative genomic hybridization data
This record last updated: 10-22-2009
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