The CNVMetrics package calculates similarity metrics to facilitate copy number variant comparison among samples and/or methods. Similarity metrics can be employed to compare CNV profiles of genetically unrelated samples as well as those with a common genetic background. Some metrics are based on the shared amplified/deleted regions while other metrics rely on the level of amplification/deletion. The data type used as input is a plain text file containing the genomic position of the copy number variations, as well as the status and/or the log2 ratio values. Finally, a visualization tool is provided to explore resulting metrics.
Package details |
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Bioconductor views | BiologicalQuestion CopyNumberVariation Software |
Maintainer | |
License | Artistic-2.0 |
Version | 1.5.1 |
URL | https://github.com/krasnitzlab/CNVMetrics https://krasnitzlab.github.io/CNVMetrics/ |
Package repository | View on GitHub |
Installation |
Install the latest version of this package by entering the following in R:
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