{"skill":{"slug":"cnv-caller-plotter","displayName":"Cnv Caller Plotter","summary":"Detect copy number variations from whole genome sequencing data and generate publication-quality genome-wide CNV plots. Supports CNV calling, segmentation, a...","tags":{"latest":"0.1.0"},"stats":{"comments":0,"downloads":184,"installsAllTime":0,"installsCurrent":0,"stars":0,"versions":1},"createdAt":1773806033569,"updatedAt":1777271496944},"latestVersion":{"version":"0.1.0","createdAt":1773806033569,"changelog":"Initial release of cnv-caller-plotter, enabling CNV detection and visualization from WGS data:\n\n- Detects copy number variations (CNVs) from whole genome sequencing (WGS) data for cancer, rare disease, and population genomics.\n- Supports input formats including BAM and VCF, with genomic segmentation and customizable bin sizes.\n- Exports CNV calls in standard BED format for downstream analysis.\n- Generates publication-quality genome-wide CNV visualization plots in PNG, PDF, or SVG.\n- Integrates with other bioinformatics skills for upstream QC and downstream analysis/visualization.","license":"MIT-0"},"metadata":null,"owner":{"handle":"aipoch-ai","userId":"s17fjw78yq6wtd4ep6zsaxwrn983hznr","displayName":"AIpoch","image":"https://avatars.githubusercontent.com/u/258999481?v=4"},"moderation":{"isSuspicious":true,"isMalwareBlocked":false,"verdict":"suspicious","reasonCodes":["suspicious.llm_suspicious"],"summary":"Detected: suspicious.llm_suspicious","engineVersion":"v2.4.0","updatedAt":1777271496944}}