jpuntomarcos/CNVfilteR: Identifies false positives of CNV calling tools by using SNV calls
CNVfilteR identifies those CNVs that can be discarded by using the single nucleotide variant (SNV) calls that are usually obtained in common NGS pipelines.
Getting started
Browse package contents
Package details |
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| Bioconductor views | CopyNumberVariation DNASeq DataImport Sequencing Visualization |
| Maintainer | |
| License | Artistic-2.0 |
| Version | 1.15.2 |
| URL | https://github.com/jpuntomarcos/CNVfilteR |
| Package repository | View on GitHub |
| Installation |
Install the latest version of this package by entering the following in R:
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