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SATS: Signature Analyzer for Targeted Sequencing (SATS)

Performs mutational signature analysis for targeted sequenced tumors. Unlike the canonical analysis of mutational signatures, SATS factorizes the mutation counts matrix into a panel context matrix (measuring the size of the targeted sequenced genome for each tumor in the unit of million base pairs (Mb)), a signature profile matrix, and a signature activity matrix. SATS also calculates the expected number of mutations attributed by a signature, namely signature burden, for each targeted sequenced tumor. For more details see Lee et al. (2024) <doi:10.1101/2023.05.18.23290188>.

Version:1.0.6
Depends:R (≥ 4.1.0)
Imports:stats,glmnet,GenomicRanges,IRanges,Biostrings,dplyr,BSgenome.Hsapiens.UCSC.hg19,BSgenome.Hsapiens.UCSC.hg38
Suggests:testthat
Published:2025-08-18
DOI:10.32614/CRAN.package.SATS
Author:DongHyuk Lee [aut], Bin Zhu [aut], Bill Wheeler [cre]
Maintainer:Bill Wheeler <wheelerb at imsweb.com>
License:GPL-2
NeedsCompilation:yes
CRAN checks:SATS results

Documentation:

Reference manual:SATS.html ,SATS.pdf

Downloads:

Package source: SATS_1.0.6.tar.gz
Windows binaries: r-devel:SATS_1.0.6.zip, r-release:SATS_1.0.6.zip, r-oldrel:SATS_1.0.6.zip
macOS binaries: r-release (arm64): not available, r-oldrel (arm64): not available, r-release (x86_64): not available, r-oldrel (x86_64): not available
Old sources: SATS archive

Linking:

Please use the canonical formhttps://CRAN.R-project.org/package=SATSto link to this page.


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