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
You Might Also Like
Red Hat Enterprise Linux (RHEL) on Microsoft Azure provides a secure, reliable, and flexible foundation for your cloud infrastructure. Red Hat Enterprise Linux on Microsoft Azure is ideal for enterprises seeking to enhance their cloud environment with seamless integration, consistent performance, and comprehensive support.
Rate This Project
Login To Rate This Project
User Reviews
-
Cnv works fine.