Package: PureCN Type: Package Title: Copy number calling and SNV classification using targeted short read sequencing Version: 2.19.0 Date: 2026-02-17 Authors@R: c(person("Markus", "Riester", role = c("aut", "cre"), email = "markus.riester@gmail.com", comment = c(ORCID = "0000-0002-4759-8332")), person("Angad P.", "Singh", role = "aut")) Description: 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. Depends: R (>= 3.5.0), DNAcopy, VariantAnnotation (>= 1.14.1) Imports: GenomicRanges (>= 1.20.3), IRanges (>= 2.2.1), RColorBrewer, S4Vectors, data.table, grDevices, graphics, stats, utils, SummarizedExperiment, Seqinfo, GenomeInfoDb, GenomicFeatures, Rsamtools, Biobase, Biostrings, BiocGenerics, rtracklayer, ggplot2, gridExtra, futile.logger, VGAM, tools, methods, mclust, rhdf5, Matrix Suggests: BiocParallel, BiocStyle, PSCBS, R.utils, TxDb.Hsapiens.UCSC.hg19.knownGene, covr, knitr, optparse, org.Hs.eg.db, jsonlite, markdown, rmarkdown, testthat Enhances: genomicsdb (>= 0.0.3) VignetteBuilder: knitr License: Artistic-2.0 BugReports: https://github.com/lima1/PureCN/issues URL: https://github.com/lima1/PureCN biocViews: CopyNumberVariation, Software, Sequencing, VariantAnnotation, VariantDetection, Coverage, ImmunoOncology NeedsCompilation: no ByteCompile: yes RoxygenNote: 7.3.1 Config/pak/sysreqs: make libbz2-dev liblzma-dev libpng-dev libxml2-dev libssl-dev xz-utils zlib1g-dev Repository: https://bioc.r-universe.dev Date/Publication: 2026-04-28 12:43:25 UTC RemoteUrl: https://github.com/bioc/PureCN RemoteRef: HEAD RemoteSha: 3bf84d2b077f90ccea86a7e2157828d2277c0e0d Packaged: 2026-07-05 10:30:31 UTC; root Author: Markus Riester [aut, cre] (ORCID: ), Angad P. Singh [aut] Maintainer: Markus Riester