Binary package “cnvkit” in ubuntu noble
Copy number variant detection from targeted DNA sequencing
A command-line toolkit and Python library for detecting copy number variants
and alterations genome-wide from targeted DNA sequencing. It is designed for
use with hybrid capture, including both whole-exome and custom target panels,
and short-read sequencing platforms such as Illumina and Ion Torrent.
Source package
Published versions
- cnvkit 0.9.9-2 in amd64 (Release)
- cnvkit 0.9.10-1 in amd64 (Proposed)
- cnvkit 0.9.10-1 in amd64 (Release)
- cnvkit 0.9.9-2 in arm64 (Release)
- cnvkit 0.9.10-1 in arm64 (Proposed)
- cnvkit 0.9.10-1 in arm64 (Release)
- cnvkit 0.9.9-2 in ppc64el (Release)
- cnvkit 0.9.10-1 in ppc64el (Proposed)
- cnvkit 0.9.10-1 in ppc64el (Release)