cnv_facets
Detect somatic copy number variants (CNV) in tumour-normal samples using next generation sequencing data
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Summary
Detect somatic copy number variants (CNV) in tumour-normal samples using next generation sequencing data
Last Updated
Sep 13, 2024 at 06:57
License
MIT
Total Downloads
43.6K
Supported Platforms
linux-64
linux-aarch64