SEA performs simultaneous feature-set testing for (gen)omics data. It tests the unified null hypothesis and controls the family-wise error rate for all possible pathways. The unified null hypothesis is defined as: "The proportion of true features in the set is less than or equal to a threshold." Family-wise error rate control is provided through use of closed testing with Simes test. There are some practical functions to play around with the pathways of interest.
Version: | 2.1.2 |
Depends: | R (≥ 2.10), hommel (≥ 1.4), ggplot2 |
Suggests: | knitr, rmarkdown |
Published: | 2024-06-11 |
DOI: | 10.32614/CRAN.package.rSEA |
Author: | Mitra Ebrahimpoor |
Maintainer: | Mitra Ebrahimpoor <mitra.ebrahimpoor at gmail.com> |
License: | GPL-2 | GPL-3 [expanded from: GPL (≥ 2)] |
NeedsCompilation: | no |
Materials: | README |
In views: | Omics |
CRAN checks: | rSEA results |
Reference manual: | rSEA.pdf |
Vignettes: |
rSEA R package |
Package source: | rSEA_2.1.2.tar.gz |
Windows binaries: | r-devel: rSEA_2.1.2.zip, r-release: rSEA_2.1.2.zip, r-oldrel: rSEA_2.1.2.zip |
macOS binaries: | r-release (arm64): rSEA_2.1.2.tgz, r-oldrel (arm64): rSEA_2.1.2.tgz, r-release (x86_64): rSEA_2.1.2.tgz, r-oldrel (x86_64): rSEA_2.1.2.tgz |
Old sources: | rSEA archive |
Reverse suggests: | ReporterScore |
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