CNViz takes probe, gene, and segment-level log2 copy number ratios and launches a Shiny app to visualize your sample's copy number profile. You can also integrate loss of heterozygosity (LOH) and single nucleotide variant (SNV) data.
Package details |
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| Bioconductor views | CopyNumberVariation DNASeq Sequencing Visualization |
| Maintainer | |
| License | Artistic-2.0 |
| Version | 1.3.1 |
| Package repository | View on GitHub |
| Installation |
Install the latest version of this package by entering the following in R:
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