CNVfilteR: Identifies false positives of CNV calling tools by using SNV calls

CNVfilteR identifies false positives produced by germline NGS copy number variant detection tools by using single nucleotide variants.

Package details

AuthorJose Marcos Moreno-Cabrera [aut, cre] (<>), Bernat Gel [aut]
Bioconductor views CopyNumberVariation DNASeq DataImport Sequencing Visualization
MaintainerJose Marcos Moreno-Cabrera <>
Package repositoryView on Bioconductor
Installation Install the latest version of this package by entering the following in R:
if (!requireNamespace("BiocManager", quietly = TRUE))


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CNVfilteR documentation built on April 17, 2021, 6:06 p.m.