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Application of 'FateID' allows computation and visualization of cell fate bias for multi-lineage single cell transcriptome data. Herman, J.S., Sagar, Grün D. (2018) <doi:10.1038/nmeth.4662>.
Version: | 0.2.2 |
Depends: | R (≥ 3.5.0) |
Imports: | graphics, grDevices, locfit, matrixStats, pheatmap, princurve, randomForest, RColorBrewer, Rtsne, som, stats, umap, utils |
Suggests: | DESeq2, knitr, rmarkdown |
Published: | 2022-06-14 |
DOI: | 10.32614/CRAN.package.FateID |
Author: | Dominic Grün |
Maintainer: | Dominic Grün <dominic.gruen at gmail.com> |
License: | GPL-3 |
NeedsCompilation: | no |
CRAN checks: | FateID results |
Reference manual: | FateID.pdf |
Vignettes: |
An introduction to FateID. |
Package source: | FateID_0.2.2.tar.gz |
Windows binaries: | r-devel: FateID_0.2.2.zip, r-release: FateID_0.2.2.zip, r-oldrel: FateID_0.2.2.zip |
macOS binaries: | r-release (arm64): FateID_0.2.2.tgz, r-oldrel (arm64): FateID_0.2.2.tgz, r-release (x86_64): FateID_0.2.2.tgz, r-oldrel (x86_64): FateID_0.2.2.tgz |
Old sources: | FateID archive |
Reverse imports: | RaceID |
Please use the canonical form https://CRAN.R-project.org/package=FateID to link to this page.
These binaries (installable software) and packages are in development.
They may not be fully stable and should be used with caution. We make no claims about them.
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