CNVkit¶
A command-line toolkit and Python library for detecting copy number variants and alterations genome-wide from high-throughput sequencing.
homepage: https://github.com/etal/cnvkit
| version | versionsuffix | toolchain |
|---|---|---|
0.9.10 |
-R-4.2.2 |
foss/2022b |
0.9.8 |
-R-4.0.3 |
foss/2020b |
(quick links: (all) - 0 - a - b - c - d - e - f - g - h - i - j - k - l - m - n - o - p - q - r - s - t - u - v - w - x - y - z)