Build a version
CNVkit is a flexible toolkit for calling copy number from DNA sequencing data. For whole-exome and targeted gene panels, off-target sequencing reads from hybrid capture are used to improve copy number estimates. Targeted amplicon capture and whole-genome sequencing protocols are also supported. CNVKit implements a variety of visualization modes, analysis methods, and output file formats for easy integration into existing pipelines.
3 days, 20 hours ago failed
.. image:: http://readthedocs.org/projects/cnvkit/badge/?version=stable :target: http://cnvkit.readthedocs.io/en/stable/?badge=stable :alt: Documentation Status
<a href='http://cnvkit.readthedocs.io/en/stable/?badge=stable'> <img src='http://readthedocs.org/projects/cnvkit/badge/?version=stable' alt='Documentation Status' /> </a>
Project Privacy Level