pathways | R Documentation |
Checks for enrichment of known or custom pathways
pathways(
maf,
pathdb = "sigpw",
pathways = NULL,
fontSize = 1,
panelWidths = c(2, 4, 4),
plotType = NA,
col = "#f39c12"
)
maf |
an |
pathdb |
Either 'sigpw' or 'smgbp', 'sigpw' uses known oncogenic signalling pathways (Sanchez/Vega et al) whereas 'smgbp' uses pan cancer significantly mutated genes classified according to biological process (Bailey et al). Default |
pathways |
Can be a two column data.frame/tsv-file with gene names and pathway-name involved in them. Default 'NULL'. This argument is mutually exclusive with |
fontSize |
Default 1 |
panelWidths |
Default c(2, 4, 4) |
plotType |
Can be 'treemap' or 'bar'. Set NA to suppress plotting. Default NA |
col |
Default #f39c12 |
Oncogenic signalling and SMG pathways are derived from TCGA cohorts. See references for details.
fraction of altered pathway. attr genes contain pathway contents
Sanchez-Vega F, Mina M, Armenia J, Chatila WK, Luna A, La KC, Dimitriadoy S, Liu DL, Kantheti HS, Saghafinia S et al. 2018. Oncogenic Signaling Pathways in The Cancer Genome Atlas. Cell 173: 321-337 e310 Bailey, Matthew H et al. “Comprehensive Characterization of Cancer Driver Genes and Mutations.” Cell vol. 173,2 (2018): 371-385.e18.
plotPathways
laml.maf <- system.file("extdata", "tcga_laml.maf.gz", package = "maftools")
laml <- read.maf(maf = laml.maf)
pathways(maf = laml)
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