Load the package with the library function.
library(tidyverse)
library(ggplot2)
library(dce)
set.seed(42)
We provide access to the following topological pathway databases using graphite (Sales et al. 2012) in a processed format. This format looks as follows:
dce::df_pathway_statistics %>%
arrange(desc(node_num)) %>%
head(10) %>%
knitr::kable()
database | pathway_id | pathway_name | node_num | edge_num |
---|---|---|---|---|
reactome | R-HSA-162582 | Signaling Pathways | 2488 | 62068 |
reactome | R-HSA-1430728 | Metabolism | 2047 | 85543 |
reactome | R-HSA-392499 | Metabolism of proteins | 1894 | 52807 |
reactome | R-HSA-1643685 | Disease | 1774 | 55469 |
reactome | R-HSA-168256 | Immune System | 1771 | 58277 |
panther | P00057 | Wnt signaling pathway | 1644 | 195344 |
reactome | R-HSA-74160 | Gene expression (Transcription) | 1472 | 32493 |
reactome | R-HSA-597592 | Post-translational protein modification | 1394 | 26399 |
kegg | hsa:01100 | Metabolic pathways | 1343 | 22504 |
reactome | R-HSA-73857 | RNA Polymerase II Transcription | 1339 | 25294 |
Let’s see how many pathways each database provides:
dce::df_pathway_statistics %>%
count(database, sort = TRUE, name = "pathway_number") %>%
knitr::kable()
database | pathway_number |
---|---|
pathbank | 48685 |
smpdb | 48671 |
reactome | 2406 |
wikipathways | 640 |
kegg | 323 |
panther | 94 |
pharmgkb | 90 |
Next, we can see how the pathway sizes are distributed for each database:
dce::df_pathway_statistics %>%
ggplot(aes(x = node_num)) +
geom_histogram(bins = 30) +
facet_wrap(~ database, scales = "free") +
theme_minimal()
It is easily possible to plot pathways:
pathways <- get_pathways(
pathway_list = list(
pathbank = c("Lactose Synthesis"),
kegg = c("Fatty acid biosynthesis")
)
)
lapply(pathways, function(x) {
plot_network(
as(x$graph, "matrix"),
visualize_edge_weights = FALSE,
arrow_size = 0.02,
shadowtext = TRUE
) +
ggtitle(x$pathway_name)
})
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sessionInfo()
## R Under development (unstable) (2024-10-21 r87258)
## Platform: x86_64-pc-linux-gnu
## Running under: Ubuntu 24.04.1 LTS
##
## Matrix products: default
## BLAS: /home/biocbuild/bbs-3.21-bioc/R/lib/libRblas.so
## LAPACK: /usr/lib/x86_64-linux-gnu/lapack/liblapack.so.3.12.0
##
## locale:
## [1] LC_CTYPE=en_US.UTF-8 LC_NUMERIC=C
## [3] LC_TIME=en_GB LC_COLLATE=C
## [5] LC_MONETARY=en_US.UTF-8 LC_MESSAGES=en_US.UTF-8
## [7] LC_PAPER=en_US.UTF-8 LC_NAME=C
## [9] LC_ADDRESS=C LC_TELEPHONE=C
## [11] LC_MEASUREMENT=en_US.UTF-8 LC_IDENTIFICATION=C
##
## time zone: America/New_York
## tzcode source: system (glibc)
##
## attached base packages:
## [1] stats4 stats graphics grDevices utils datasets methods
## [8] base
##
## other attached packages:
## [1] dce_1.13.0 graph_1.83.0
## [3] cowplot_1.1.3 lubridate_1.9.3
## [5] forcats_1.0.0 stringr_1.5.1
## [7] dplyr_1.1.4 purrr_1.0.2
## [9] readr_2.1.5 tidyr_1.3.1
## [11] tibble_3.2.1 tidyverse_2.0.0
## [13] TCGAutils_1.25.1 curatedTCGAData_1.27.1
## [15] MultiAssayExperiment_1.31.5 SummarizedExperiment_1.35.5
## [17] Biobase_2.65.1 GenomicRanges_1.57.2
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## [21] S4Vectors_0.43.2 BiocGenerics_0.51.3
## [23] MatrixGenerics_1.17.1 matrixStats_1.4.1
## [25] ggraph_2.2.1 ggplot2_3.5.1
## [27] BiocStyle_2.33.1
##
## loaded via a namespace (and not attached):
## [1] bitops_1.0-9 httr_1.4.7
## [3] GenomicDataCommons_1.29.7 prabclus_2.3-4
## [5] Rgraphviz_2.49.1 numDeriv_2016.8-1.1
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## [21] sass_0.4.9 diptest_0.77-1
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## [27] FMStable_0.1-4 Linnorm_2.29.0
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