
Plot pathway-specific expression heatmaps from enrichment output
get_pathway_heatmap.RdThis wrapper bridges enrichment results and expression heatmaps. It extracts
genes from selected pathways (via get_pathway_genes()), maps them to the
VISTA feature IDs, and forwards to get_expression_heatmap().
Usage
get_pathway_heatmap(
vista_obj,
enrichment,
samples,
pathways = NULL,
top_n = 5,
pathway_column = c("Description", "ID"),
gene_column = c("auto", "geneID", "core_enrichment"),
gene_sep = "/",
gene_mode = c("union", "intersection"),
gene_id_column = NULL,
max_genes = NULL,
return_type = c("heatmap", "both", "genes"),
...
)Arguments
- vista_obj
A
VISTAobject.- enrichment
An
enrichResult/gseaResult, or a list with elementenrichas returned byget_*_enrichment()helpers.- samples
Character vector of group labels to include (same semantics as
get_expression_heatmap()).- pathways
Optional pathway names to include. When
NULL, top pathways are selected usingtop_n.- top_n
Number of top pathways used when
pathways = NULL. Default:5.- pathway_column
Pathway matching column,
"Description"(default) or"ID".- gene_column
Pathway gene-member column.
"auto"uses"geneID"or"core_enrichment"based on availability.- gene_sep
Delimiter used to parse pathway gene strings (default
"/").- gene_mode
How to combine pathway genes for plotting:
"union"(default) or"intersection".- gene_id_column
Optional column in
rowData(vista_obj)used to map enrichment genes back to VISTA rownames (e.g.,"SYMBOL"or"ENTREZID"). LeaveNULLwhen enrichment genes already match VISTA rownames.- max_genes
Optional cap on the number of genes passed to the heatmap.
- return_type
One of
"heatmap"(default),"both", or"genes".- ...
Additional arguments passed to
get_expression_heatmap().
Value
Depending on return_type:
"heatmap": aComplexHeatmapobject fromget_expression_heatmap()."both": list withheatmap,genes, andpathway_genes."genes": character vector of mapped genes selected for plotting.
Examples
if (FALSE) { # \dontrun{
data("count_data", package = "VISTA")
data("sample_metadata", package = "VISTA")
vista <- create_vista(
counts = count_data,
sample_info = sample_metadata,
column_geneid = "gene_id",
group_column = "cond_long",
group_numerator = "treatment1",
group_denominator = "control"
)
msig <- get_msigdb_enrichment(
vista,
sample_comparison = names(comparisons(vista))[1],
regulation = "Up",
species = "Homo sapiens",
from_type = "ENSEMBL"
)
get_pathway_heatmap(
vista,
enrichment = msig,
samples = c("control", "treatment1"),
top_n = 3,
value_transform = "zscore",
annotate_columns = TRUE,
summarise_replicates = FALSE
)
} # }