Call copy number variants using GATK best practices workflow. Supports both somatic (tumor-normal) and germline CNV detection from WGS or WES data. Use when following GATK best practices or integrating CNV calling with other GATK variant pipelines.
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Skill Details
GitHub Stars
300
GitHub Forks
51
Created
Jan 2026
Last Updated
5 months ago
tools
tools bioinformatics
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