The easiest way to analyze one, ten, or even hundreds of human genomes - all on a standard desktop or laptop computer.
Import and annotate your data with a few clicks. Filter millions of variations with an effortless and effective query builder. Integrate the analysis of small variation data with call coverage, structural variation, and copy number changes.
Designed for intuitive use. Easy enough to be used by a wet lab biologist or clinician. Powerful enough for the more experienced bioinformatician.
"Software that would most substantially improve the scientific utility of genomic data..."
The overall winner of the Illumina Data Excellence Award competition is now available!
Great for the analysis of: