Supported Applications
CNVkit
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Description
a command-line toolkit and Python library for detecting copy number variants and alterations genome-wide from high-throughput sequencing.
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Installation
Use the following command to install this title with the CLI client:$ biogrids-cli install cnvkit
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Primary Citation*
E. Talevich, A. H. Shain, T. Botton, and B. BC.. 2016. CNVkit: Genome-Wide Copy Number Detection and Visualization from Targeted DNA Sequencing. PLoS Comput Biol. 12(4).
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*Full citation information available through
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Keywords
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Default Versions
Linux 64:  0.9.7
OS X INTEL:  0.9.7 -
Other Versions
Linux 64:
0.9.6 -
OS X INTEL:
0.9.6