Workflow for Sequenza, cellularity and ploidy
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Updated
Jun 27, 2024 - R
Workflow for Sequenza, cellularity and ploidy
An R package for detecting copy number variants from SNPs data
VizCNV is an interactive tool designed to analyze and visualize CNVs from short read WGS data in rare disease research. Built on R Studio Shiny, it streamlines the identification of complex genomic rearrangements and facilitates advancements in understanding and diagnosing rare genetic conditions.
An R package to integrate and analyze CNV calling results from multiple methods in a uniformed and standardized manner
Powerful CNV calls filtering pipeline. Focused on fixed loci calling, before visual inspection.
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