Segmentation of allele-specific DNA copy number data and detection of regions with abnormal copy number within each parental chromosome. Both tumor-normal paired and tumor-only analyses are supported.
Version: |
0.67.0 |
Depends: |
R (≥ 3.2.0) |
Imports: |
R.methodsS3 (≥ 1.8.2), R.oo (≥ 1.25.0), R.utils (≥ 2.12.0), R.cache (≥ 0.16.0), matrixStats (≥ 0.62.0), aroma.light (≥
2.4.0), DNAcopy (≥ 1.42.0), listenv (≥ 0.8.0), future (≥
1.28.0), parallel, graphics, grDevices, stats, utils |
Suggests: |
R.rsp (≥ 0.45.0), R.devices (≥ 2.17.1), ggplot2 (≥ 3.2.1) |
Published: |
2024-02-17 |
DOI: |
10.32614/CRAN.package.PSCBS |
Author: |
Henrik Bengtsson [aut, cre, cph],
Pierre Neuvial [aut],
Venkatraman E. Seshan [aut],
Adam B. Olshen [aut],
Paul T. Spellman [aut],
Richard A. Olshen [aut],
Frank E Harrell Jr [ctb] (Weighted quantile estimator adopted from
Hmisc::wtd.quantile()) |
Maintainer: |
Henrik Bengtsson <henrikb at braju.com> |
BugReports: |
https://github.com/HenrikBengtsson/PSCBS/issues |
License: |
GPL-2 | GPL-3 [expanded from: GPL (≥ 2)] |
URL: |
https://github.com/HenrikBengtsson/PSCBS |
NeedsCompilation: |
no |
Citation: |
PSCBS citation info |
Materials: |
README NEWS |
In views: |
Omics |
CRAN checks: |
PSCBS results |