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bio-copy-number-cnvkit-analysis

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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.

When to use

• Detecting CNVs from WES
• Detecting CNVs from targeted panel sequencing
• Tumor-normal pair analysis
• Tumor-only CNV calling
• Germline CNV calling
• WGS mode CNV detection
• bedGraph input processing

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