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CNV Workshop is a web-enabled platform for analyzing genome variation such as copy number variation (CNV). Learn about CNV Workshop in our associated BMC Bioinformatics manuscript: http://www.biomedcentral.com/1471-2105/11/74
Features
- Compute CNV calls using a high-quality published algorithm, on or off a cluster
- Publish/view CNV calls via a sophisticated web application
- Visualize your CNVs in GBrowse and UCSC genome browser
- Support multiple labs/groups via user and group membership
- Download in XLS, CSV, XML, BED, and PDF format
- View GAD phenotype, DGV CNV, and gene annotation
- Compare your CNVs against the CHOP normals data set (healthy controls)
- View hyperdiploidy/LOH reports
- Link out to FABLE, Entrez, Entrez Gene, GAD, DGV, UCSC
Categories
Bio-InformaticsLicense
Affero GNU Public LicenseFollow CNV Workshop
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User Reviews
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Cnv works fine.
