About CNV Workshop
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: Features Compute CNV calls using a...
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:
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
Previous Versions
Here you can find the changelog of CNV Workshop since it was posted on our website on 2015-04-25 03:00:00.
The latest version is 2.0.11 and it was updated on 2024-04-22 16:06:06. See below the changes in each version.
CNV Workshop version
Updated At: 2010-10-25
CNV Workshop version files
Updated At: 2010-10-25
Changes: Several fixes and updates
Disclaimer
External Download
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