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# decoupleR <img src="inst/figures/logo.svg" align="right" width="120" />
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## Overview
There are many methods that allow us to extract biological activities
from omics data. `decoupleR` is a Bioconductor package containing
different statistical methods to extract biological signatures from
prior knowledge within a unified framework. Additionally, it
incorporates methods that take into account the sign and weight of
network interactions. `decoupleR` can be used with any omic, as long as
its features can be linked to a biological process based on prior
knowledge. For example, in transcriptomics gene sets regulated by a
transcription factor, or in phospho-proteomics phosphosites that are
targeted by a kinase.
<p align="center" width="100%">
<img src="https://github.com/saezlab/decoupleR/blob/master/inst/figures/graphical_abstract.png?raw=1" align="center" width="45%">
</p>
For more information about how this package has been used with real
data, please check the following links:
- [decoupleR’s
vignette](https://saezlab.github.io/decoupleR/articles/decoupleR.html)
- [Python
implementation](https://decoupler-py.readthedocs.io/en/latest/)
- [decoupleR’s manuscript
repository](https://github.com/saezlab/decoupleR_manuscript)
- [Creation of benchmarking
pipelines](https://github.com/saezlab/decoupleRBench)
- [Example of Kinase and TF activity
estimation](https://saezlab.github.io/kinase_tf_mini_tuto/)
# Installation
`decoupleR` is an R package distributed as part of the Bioconductor
project. To install the package, start R and enter:
``` r
install.packages("BiocManager")
BiocManager::install("decoupleR")
```
Alternatively, you can instead install the latest development version
from [GitHub](https://github.com/) with:
``` r
BiocManager::install("saezlab/decoupleR")
```
## Citation
Badia-i-Mompel P., Vélez Santiago J., Braunger J., Geiss C., Dimitrov
D., Müller-Dott S., Taus P., Dugourd A., Holland C.H., Ramirez Flores
R.O. and Saez-Rodriguez J. 2022. decoupleR: ensemble of computational
methods to infer biological activities from omics data. Bioinformatics
Advances. <https://doi.org/10.1093/bioadv/vbac016>
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