You do not have permission to edit this page, for the following reason:
The action you have requested is limited to users in the group: Users.
Short description:
Please summarise the application in a few sentences. Avoid links here. CNV-seq, a method to detect copy number variation using high-throughput sequencing. [http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pubmed&pubmedid=19267900 pubmed]
Software version:
Biological application domain(s) (Phylogenetics, Genomics, ...):
Copy number estimation
Principal bioinformatics method(s) (Assembly, Mapping, ...):
Technology (Sanger, Illumina, 454, SOLiD, Ion Torrent, ...):
Interface (Command line, Web UI, Desktop GUI, SOAP WS, HTTP WS, API, QL):
Resource type (Command-line tool, Web application, Desktop application, Script, Suite, Workbench, Database portal, Workflow, Plug-in, Library, Web API, Web service, SPARQL endpoint):
Link: http://tiger.dbs.nus.edu.sg/CNV-seq/ Category: CNV
Once you save the form, you will have the chance to add links and references.
Summary of edit
This is a minor edit Watch this page
Cancel