View source: R/fct_06_pathway.R
gage_data | R Documentation |
Run pathway analysis with the gage package using the results from the limma_value function.
gage_data(
select_go,
select_contrast,
min_set_size,
max_set_size,
limma,
gene_p_val_cutoff,
gene_sets,
absolute_fold,
pathway_p_val_cutoff,
n_pathway_show
)
select_go |
String designating the section of the database to query for
pathway analysis. See |
select_contrast |
String designating the comparison from DEG analysis to
filter for the significant genes. See the 'comparison' element from the list
returned from |
min_set_size |
Minimum gene set size for a pathway |
max_set_size |
Maximum gene set size for a pathway |
limma |
Results list from the |
gene_p_val_cutoff |
Significant p-value to filter the top genes fold change by |
gene_sets |
List of vectors with each vector being the
set of genes that correspond to a particular pathway in
the database. See list returned from |
absolute_fold |
TRUE/FALSE to use the absolute value of the fold change |
pathway_p_val_cutoff |
Significant p-value to determine enriched pathways |
n_pathway_show |
Number of pathways to return in final result |
A data frame with the results of the pathway analysis. The data frame has five columns for the direction of the regulation, the pathway description, the stat value, the number of overlapping genes, and the p-value.
Other pathway functions:
fgsea_data()
,
find_overlap()
,
get_gsva_plot_data()
,
get_pathway_list_data()
,
get_pgsea_plot_all_samples_data()
,
get_pgsea_plot_data()
,
gsva_data()
,
kegg_pathway()
,
pathway_select_data()
,
pgsea_data()
,
pgsea_plot_all()
,
plot_gsva()
,
plot_pgsea()
,
reactome_data()
,
remove_pathway_id()
,
remove_pathway_id_second()
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