--- /srv/rebuilderd/tmp/rebuilderdgim7Ak/inputs/r-bioc-purecn_2.12.0+dfsg-2_all.deb
+++ /srv/rebuilderd/tmp/rebuilderdgim7Ak/out/r-bioc-purecn_2.12.0+dfsg-2_all.deb
├── file list
│ @@ -1,3 +1,3 @@
│  -rw-r--r--   0        0        0        4 2025-01-14 07:56:53.000000 debian-binary
│ --rw-r--r--   0        0        0     3704 2025-01-14 07:56:53.000000 control.tar.xz
│ +-rw-r--r--   0        0        0     3648 2025-01-14 07:56:53.000000 control.tar.xz
│  -rw-r--r--   0        0        0  6021104 2025-01-14 07:56:53.000000 data.tar.xz
├── control.tar.xz
│ ├── control.tar
│ │ ├── file list
│ │ │ @@ -1,3 +1,3 @@
│ │ │  drwxr-xr-x   0 root         (0) root         (0)        0 2025-01-14 07:56:53.000000 ./
│ │ │ --rw-r--r--   0 root         (0) root         (0)     1427 2025-01-14 07:56:53.000000 ./control
│ │ │ +-rw-r--r--   0 root         (0) root         (0)     1262 2025-01-14 07:56:53.000000 ./control
│ │ │  -rw-r--r--   0 root         (0) root         (0)     8718 2025-01-14 07:56:53.000000 ./md5sums
│ │ ├── ./control
│ │ │ @@ -1,14 +1,14 @@
│ │ │  Package: r-bioc-purecn
│ │ │  Version: 2.12.0+dfsg-2
│ │ │  Architecture: all
│ │ │  Maintainer: Debian R Packages Maintainers <r-pkg-team@alioth-lists.debian.net>
│ │ │  Installed-Size: 6928
│ │ │  Depends: r-api-4.0, r-api-bioc-3.20, r-bioc-dnacopy, r-bioc-variantannotation (>= 1.14.1), r-bioc-genomicranges (>= 1.20.3), r-bioc-iranges (>= 2.2.1), r-cran-rcolorbrewer, r-bioc-s4vectors, r-cran-data.table, r-bioc-summarizedexperiment, r-bioc-genomeinfodb, r-bioc-genomicfeatures, r-bioc-rsamtools, r-bioc-biobase, r-bioc-biostrings, r-bioc-biocgenerics, r-bioc-rtracklayer, r-cran-ggplot2, r-cran-gridextra, r-cran-futile.logger, r-cran-vgam, r-cran-mclust, r-bioc-rhdf5, r-cran-matrix
│ │ │ -Suggests: r-bioc-biocparallel, r-bioc-biocstyle, r-cran-pscbs, r-cran-r.utils, r-cran-covr, r-cran-knitr, r-cran-optparse, r-bioc-org.hs.eg.db, r-cran-jsonlite, r-cran-markdown, r-cran-rmarkdown, r-cran-testthat
│ │ │ +Suggests: r-bioc-biocparallel, r-cran-jsonlite
│ │ │  Section: gnu-r
│ │ │  Priority: optional
│ │ │  Homepage: https://bioconductor.org/packages/PureCN/
│ │ │  Description: copy number calling and SNV classification using targeted short read sequencing
│ │ │   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