CCNV: a user-friendly R package enabling large-scale cumulative copy number variation analyses of DNA methylation data

CCNV is a user-friendly R package, which enables fast and accurate generation and analyses of cumulative copy number variation plots.

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Publication Details

Journal
BMC Bioinformatics
Published
2025-09-23
DOI
https://doi.org/10.1186/s12859-025-06269-z
Primary Topic
Genomic variations and chromosomal abnormalities
Type
article
Field-Weighted Citation Impact
0.00

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article

CCNV: a user-friendly R package enabling large-scale cumulative copy number variation analyses of DNA methylation data

Matthias Dottermusch, Julia E. Neumann, Melanie Schoof, Yannis Schumann et al.
BMC Bioinformatics
Genomic variations and chromosomal abnormalities
article

CCNV: a user-friendly R package enabling large-scale cumulative copy number variation analyses of DNA methylation data

Matthias Dottermusch, Julia E. Neumann, Melanie Schoof, Yannis Schumann, Shweta Godbole, Jelena Navolić, Antonia Gocke
article en

Abstract

CCNV is a user-friendly R package, which enables fast and accurate generation and analyses of cumulative copy number variation plots.

BMC BioinformaticsVol. 26(1)
Universität Hamburg (DE), Deutsches Elektronen-Synchrotron DESY (DE), University Medical Center Hamburg-Eppendorf (DE), Kinderkrebs-Zentrum Hamburg (DE)
European Commission, Deutsches Elektronen-Synchrotron
Openalex Percentile: Top 72%
Genomic variations and chromosomal abnormalities
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