Cluster user-supplied somatic read counts with corresponding allele-specific copy number and tumor purity to infer feasible underlying intra-tumor heterogeneity in terms of number of subclones, multiplicity, and allocation (Little et al. (2019) <doi:10.1186/s13073-019-0643-9>).
Version: | 1.0.0 |
Depends: | R (≥ 2.10) |
Imports: | Rcpp, stats, smarter, reshape2, ggplot2 |
LinkingTo: | Rcpp, RcppArmadillo |
Suggests: | knitr, devtools |
Published: | 2025-02-27 |
DOI: | 10.32614/CRAN.package.SMASH |
Author: | Paul Little [aut, cre] |
Maintainer: | Paul Little <pllittle321 at gmail.com> |
License: | GPL (≥ 3) |
NeedsCompilation: | yes |
Citation: | SMASH citation info |
CRAN checks: | SMASH results |
Reference manual: | SMASH.pdf |
Vignettes: |
test (source, R code) |
Package source: | SMASH_1.0.0.tar.gz |
Windows binaries: | r-devel: not available, r-release: not available, r-oldrel: SMASH_1.0.0.zip |
macOS binaries: | r-devel (arm64): SMASH_1.0.0.tgz, r-release (arm64): SMASH_1.0.0.tgz, r-oldrel (arm64): SMASH_1.0.0.tgz, r-devel (x86_64): SMASH_1.0.0.tgz, r-release (x86_64): SMASH_1.0.0.tgz, r-oldrel (x86_64): SMASH_1.0.0.tgz |
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