cnv-caller-plotter
Detect copy number variations from whole genome sequencing data and generate publication-quality genome-wide CNV plots. Supports CNV calling, segmentation, tumor-normal comparison, and BED format export for cancer genomics and rare disease analysis.
78
Quality
73%
Does it follow best practices?
Impact
Pending
No eval scenarios have been run
Securityby
Passed
No known issues
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- Repository
- aipoch/medical-research-skills
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ca9aaa4
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