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bio-copy-number-cnvkit-analysis
skilltested · static-verifiedscore 20/100signed passport ✓published 264d ago · verified 2026-10-240 uses
Detect copy number variants from targeted/exome sequencing using CNVkit. Supports tumor-normal pairs, tumor-only, and germline CNV calling. Use when detecting CNVs from WES or targeted panel sequencing data.
Declared tools (1)
bio-copy-number-cnvkit-analysis
skill:gptomics/bioskills/cnvkit-analysis · published by gptomics · source repository