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SGI: automatic clinical subgroup identification in omics datasets

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SGI: Automatic clinical subgroup identification in omics datasets

Introduction

SGI workflow.

The 'Subgroup Identification' (SGI) toolbox provides an algorithm to automatically detect clinical subgroups of samples in large-scale omics datasets. It is based on hierarchical clustering trees in combination with a specifically designed association testing and visualization framework that can process a large number of clinical parameters and outcomes in a systematic fashion. A multi-block extension allows for the simultaneous use of multiple omics datasets on the same samples.

Reference

Buyukozkan, et al. "SGI: Automatic clinical subgroup identification in omics datasets". Bioinformatics, 2021. link to publication

Installation instructions

SGI can be installed as follows:

require(devtools)
devtools::install_github(repo="krumsieklab/sgi", subdir="sgi")

Getting started

Here are a few lines of code that demostrate how SGI works:

library(sgi)
# hierarchical clustering
hc = hclust(dist(sgi::qmdiab_plasma), method = "ward.D2")
# initialize SGI structure; minsize is set to 5% of sample size
sg = sgi_init(hc, minsize = 18, outcomes = sgi::qmdiab_clin)
# run SGI
as = sgi_run(sg)
# generate tree plot, show results for adjusted p-values <0.05
gg_tree = plot(as, padj_th = 0.05)
# plot overview, including clinical data and metabolomics data matrix
plot_overview( gg_tree = gg_tree, as = as, 
               outcomes = sgi::qmdiab_clin, 
               xdata    = sgi::qmdiab_plasma )

Tutorials

For more detailed examples and functionalities of the package, we provide the following tutorials:

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