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 |
0.9.2 |
-Python-2.7.14 |
intel/2017b |
0.9.3 |
-Python-3.6.4 |
intel/2018a |
0.9.6 |
-Python-3.7.2-R-3.6.0 |
foss/2019a |
0.9.8 |
-R-4.0.3 |
foss/2020b |
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