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.
Authors
- Matthias Dottermusch (ORCID: https://orcid.org/0000-0002-9769-7080)
- Julia E. Neumann (ORCID: https://orcid.org/0000-0002-1162-8771)
- Melanie Schoof (ORCID: https://orcid.org/0000-0002-1373-8130)
- Yannis Schumann (ORCID: https://orcid.org/0000-0002-2379-200X)
- Shweta Godbole (ORCID: https://orcid.org/0000-0002-5162-5233)
- Jelena Navolić (ORCID: https://orcid.org/0009-0005-2112-3987)
- Antonia Gocke (ORCID: https://orcid.org/0009-0007-5828-6637)
Institutions
- Universität Hamburg (DE)
- Deutsches Elektronen-Synchrotron DESY (DE)
- University Medical Center Hamburg-Eppendorf (DE)
- Kinderkrebs-Zentrum Hamburg (DE)
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
Funders
- European Commission
- Deutsches Elektronen-Synchrotron