decoupleR is an R package distributed as part of the Bioconductor project. To install the package, start R and enter:
Alternatively, you can instead install the latest development version from GitHub with:
decoupleR (Badia-i-Mompel, Santiago, Braunger, Geiss, Dimitrov, Müller-Dott, Taus, Dugourd, Holland, Flores, and Saez-Rodriguez, 2022) contains different statistical methods to extract biological activities from omics data using prior knowledge. Some of them are:
In this vignette we showcase how to use it with some toy data.
decoupleR can be imported as:
decoupleR
needs a matrix (mat
) of any molecular readouts (gene
expression, logFC, p-values, etc.) and a network
that
relates target features (genes, proteins, etc.) to “source” biological
entities (pathways, transcription factors, molecular processes, etc.).
Some methods also require the mode of regulation (MoR) for each
interaction, defined as negative or positive weights.
To get an example data-set, run:
data <- get_toy_data()
mat <- data$mat
head(mat,5)[,1:5]
#> S01 S02 S03 S04 S05
#> G01 9.3709584 9.3888607 9.8951935 8.7844590 8.431446
#> G02 8.5646982 8.2787888 8.4304691 8.8509076 8.655648
#> G03 8.3631284 8.1333213 8.2572694 10.4142076 8.321925
#> G04 8.6328626 8.6359504 9.7631631 8.0361226 8.783839
#> G05 0.4042683 0.2842529 0.4600974 0.2059986 1.575728
network <- data$network
network
#> # A tibble: 10 × 3
#> source target mor
#> <chr> <chr> <dbl>
#> 1 T1 G01 1
#> 2 T1 G02 1
#> 3 T1 G03 0.7
#> 4 T2 G06 1
#> 5 T2 G07 0.5
#> 6 T2 G08 1
#> 7 T3 G06 -0.5
#> 8 T3 G07 -3
#> 9 T3 G08 -1
#> 10 T3 G11 1
This example consists of two small populations of samples (S, cols) with different gene expression patterns (G, rows):
Here we can see that some genes seem to be more expressed in one group of samples than in the other and vice-versa. Ideally, we would like to capture these differences in gene programs into interpretable biological entities. In this example we will do it by summarizing gene expression into transcription factor activities.
The toy data also contains a simple net consisting of 3 transcription factors (Ts) with specific regulation to target genes (either positive or negative). This network can be visualized like a graph. Green edges are positive regulation (activation), red edges are negative regulation (inactivation):
According to this network, the first population of samples should show high activity for T1 and T3, while the second one only for T2.
decoupleR contains several methods. To check how many are available, run:
show_methods()
#> # A tibble: 12 × 2
#> Function Name
#> <chr> <chr>
#> 1 run_aucell AUCell
#> 2 run_consensus Consensus score between methods
#> 3 run_fgsea Fast Gene Set Enrichment Analysis (FGSEA)
#> 4 run_gsva Gene Set Variation Analysis (GSVA)
#> 5 run_mdt Multivariate Decision Trees (MDT)
#> 6 run_mlm Multivariate Linear Model (MLM)
#> 7 run_ora Over Representation Analysis (ORA)
#> 8 run_udt Univariate Decision Tree (UDT)
#> 9 run_ulm Univariate Linear Model (ULM)
#> 10 run_viper Virtual Inference of Protein-activity by Enriched Regulon anal…
#> 11 run_wmean Weighted Mean (WMEAN)
#> 12 run_wsum Weighted Sum (WSUM)
Each method models biological activities in a different manner,
sometimes returning more than one estimate or providing significance of
the estimation. To know what each method returns, please check their
documentation like this ?run_mlm
.
To have a unified framework, methods have these shared arguments:
mat
: input matrix of molecular readouts.network
: input prior knowledge information relating
molecular features to biological entities..source
,.target
and .mor
:
column names where to extract the information from network
.
.source
refers to the biological entities..target
refers to the molecular features..mor
refers to the “strength” of the interaction (if
available, else 1s will be used). Only available for methods that can
model interaction weights.minsize
: Minimum of target features per biological
entity (5 by default). If less, sources are removed. This filtering
prevents obtaining noisy activities from biological entities with very
few matching target features in matrix
. For this example
data-set we will have to keep it to 0 though.As an example, let’s first run the Gene Set Enrichment Analysis
method (gsea
), one of the most well-known statistics:
res_gsea <- run_fgsea(mat, network, .source='source', .target='target', nproc=1, minsize = 0)
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res_gsea
#> # A tibble: 144 × 5
#> statistic source condition score p_value
#> <chr> <chr> <chr> <dbl> <dbl>
#> 1 fgsea T1 S01 0.889 0.0755
#> 2 norm_fgsea T1 S01 1.24 0.0755
#> 3 fgsea T2 S01 -0.667 0.548
#> 4 norm_fgsea T2 S01 -1.11 0.548
#> 5 fgsea T3 S01 -0.75 0.01
#> 6 norm_fgsea T3 S01 Inf 0.01
#> 7 fgsea T1 S02 0.889 0.0764
#> 8 norm_fgsea T1 S02 1.29 0.0764
#> 9 fgsea T2 S02 0 0.977
#> 10 norm_fgsea T2 S02 0 0.977
#> # ℹ 134 more rows
Methods return a result data-frame containing:
statistic
: name of the statistic. Depending on the
method, there can be more than one per method.source
: name of the biological entity.condition
: sample name.score
: inferred biological activity.p_value
: if available, significance of the inferred
activity.In the case of gsea
, it returns a simple estimate of
activities (fgsea
), a normalized estimate
(norm_fgsea
) and p-values after doing permutations.
Other methods can return different things, for example Univariate
Linear Model (ulm
):
res_ulm <- run_ulm(mat, network, .source='source', .target='target', .mor='mor', minsize = 0)
res_ulm
#> # A tibble: 72 × 5
#> statistic source condition score p_value
#> <chr> <chr> <chr> <dbl> <dbl>
#> 1 ulm T1 S01 4.21 0.00180
#> 2 ulm T1 S02 4.07 0.00224
#> 3 ulm T1 S03 3.85 0.00319
#> 4 ulm T1 S04 4.60 0.000979
#> 5 ulm T1 S05 3.90 0.00298
#> 6 ulm T1 S06 3.66 0.00442
#> 7 ulm T1 S07 4.31 0.00153
#> 8 ulm T1 S08 4.65 0.000902
#> 9 ulm T1 S09 4.49 0.00117
#> 10 ulm T1 S10 4.07 0.00225
#> # ℹ 62 more rows
In this case, ulm
returns just an estimate
(ulm
) and its associated p-values. Each method can return
different statistics, we recommend to check their documentation to know
more about them.
Let us plot the obtained results, first for gsea
:
# Transform to matrix
mat_gsea <- res_gsea %>%
filter(statistic=='fgsea') %>%
pivot_wider_profile(id_cols = source, names_from = condition,
values_from = score) %>%
as.matrix()
pheatmap(mat_gsea, cluster_rows = F, cluster_cols = F, cellwidth = 15, cellheight = 40)
We can observe that for transcription factors T1 and T2, the obtained
activities correctly distinguish the two sample populations. T3, on the
other hand, should be down for the second population of samples since it
is a repressor. This mislabeling of activities happens because
gsea
cannot model weights when inferring biological
activities.
When weights are available in the prior knowledge, we definitely
recommend using any of the methods that take them into account to get
better estimates, one example is ulm
:
# Transform to matrix
mat_ulm <- res_ulm %>%
filter(statistic=='ulm') %>%
pivot_wider_profile(id_cols = source, names_from = condition,
values_from = score) %>%
as.matrix()
pheatmap(mat_ulm, cluster_rows = F, cluster_cols = F, cellwidth = 15, cellheight = 40)
Since ulm
models weights when estimating biological
activities, it correctly assigns T3 as inactive in the second population
of samples.
decoupleR
also allows to run multiple methods at the same time. Moreover, it
computes a consensus score based on the obtained activities across
methods, called consensus
.
By default, deocuple
runs only the top performer methods
in our benchmark (mlm
, ulm
and
wsum
), and estimates a consensus score across them.
Specific arguments to specific methods can be passed using the variable
args
. For more information check
?decouple
.
res_decouple <- decouple(mat,
network,
.source='source',
.target='target',
minsize = 0)
res_decouple
#> # A tibble: 432 × 6
#> run_id statistic source condition score p_value
#> <dbl> <chr> <chr> <chr> <dbl> <dbl>
#> 1 1 mlm T1 S01 3.52 0.00781
#> 2 1 mlm T2 S01 -1.13 0.290
#> 3 1 mlm T3 S01 -0.247 0.811
#> 4 1 mlm T1 S02 3.48 0.00831
#> 5 1 mlm T2 S02 -0.213 0.837
#> 6 1 mlm T3 S02 -0.353 0.733
#> 7 1 mlm T1 S03 3.15 0.0135
#> 8 1 mlm T2 S03 -0.638 0.541
#> 9 1 mlm T3 S03 0.0749 0.942
#> 10 1 mlm T1 S04 3.82 0.00512
#> # ℹ 422 more rows
Let us see the result for the consensus score in the previous
decouple
run:
# Transform to matrix
mat_consensus <- res_decouple %>%
filter(statistic=='consensus') %>%
pivot_wider_profile(id_cols = source, names_from = condition,
values_from = score) %>%
as.matrix()
pheatmap(mat_consensus, cluster_rows = F, cluster_cols = F, cellwidth = 15, cellheight = 40)
We can observe that the consensus score correctly predicts that T1 and T3 should be active in the first population of samples while T2 in the second one.
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[4] S. Hänzelmann, R. Castelo, and J. Guinney. “GSVA: gene set variation analysis for microarray and RNA-Seq data”. In: BMC Bioinformatics 14 (2013), p. 7. DOI: 10.1186/1471-2105-14-7. URL: https://doi.org/10.1186/1471-2105-14-7.
[5] G. Korotkevich, V. Sukhov, and A. Sergushichev. “Fast gene set enrichment analysis”. In: bioRxiv (2019). DOI: 10.1101/060012. URL: http://biorxiv.org/content/early/2016/06/20/060012.