# -------------------------------------------- # CITATION file created with {cffr} R package # See also: https://docs.ropensci.org/cffr/ # -------------------------------------------- cff-version: 1.2.0 message: 'To cite package "PureCN" in publications use:' type: software license: Artistic-2.0 title: 'PureCN: Copy number calling and SNV classification using targeted short read sequencing' version: 2.18.0 doi: 10.1186/s13029-016-0060-z identifiers: - type: doi value: 10.32614/CRAN.package.PureCN abstract: This package estimates tumor purity, copy number, and loss of heterozygosity (LOH), and classifies single nucleotide variants (SNVs) by somatic status and clonality. PureCN is designed for targeted short read sequencing data, integrates well with standard somatic variant detection and copy number pipelines, and has support for tumor samples without matching normal samples. authors: - family-names: Riester given-names: Markus email: markus.riester@gmail.com orcid: https://orcid.org/0000-0002-4759-8332 - family-names: Singh given-names: Angad P. preferred-citation: type: article title: 'PureCN: Copy number calling and SNV classification using targeted short read sequencing' authors: - family-names: Riester given-names: Markus email: markus.riester@gmail.com orcid: https://orcid.org/0000-0002-4759-8332 - family-names: Singh given-names: Angad - family-names: Brannon given-names: A. Rose - family-names: Yu given-names: Kun - family-names: Campbell given-names: Catarina D. - family-names: Chiang given-names: Derek Y. - family-names: Morrissey given-names: Michael year: '2016' volume: '11' doi: 10.1186/s13029-016-0060-z journal: Source Code for Biology and Medicine start: '13' repository: https://bioc-release.r-universe.dev repository-code: https://github.com/lima1/PureCN commit: 180d5c32bd698780ce2433dac525e808580ed458 url: https://github.com/lima1/PureCN date-released: '2026-02-17' contact: - family-names: Riester given-names: Markus email: markus.riester@gmail.com orcid: https://orcid.org/0000-0002-4759-8332