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

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

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.

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README.md CNVfilteR: Remove false positives of CNV calling tools by using SNV calls

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Package details
AuthorJose Marcos Moreno-Cabrera [aut, cre] (<https://orcid.org/0000-0001-8570-0345>), Bernat Gel [aut]
Bioconductor views CopyNumberVariation DNASeq DataImport Sequencing Visualization
MaintainerJose Marcos Moreno-Cabrera <jpuntomarcos@gmail.com>
LicenseArtistic-2.0
Version1.4.2
URL https://github.com/jpuntomarcos/CNVfilteR 
Package repositoryView on Bioconductor
Installation Install the latest version of this package by entering the following in R: 
if (!requireNamespace("BiocManager", quietly = TRUE))
    install.packages("BiocManager")

BiocManager::install("CNVfilteR")

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

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