View source: R/fct_06_pathway.R
reactome_data | R Documentation |
Run pathway analysis with the reactome package using the results from the limma_value function.
reactome_data(
select_contrast,
my_range,
limma,
gene_p_val_cutoff,
converted,
idep_data,
pathway_p_val_cutoff,
n_pathway_show,
absolute_fold
)
select_contrast |
String designating the comparison from DEG analysis to
filter for the significant genes. See the 'comparison' element from the list
returned from |
my_range |
Vector of the (min_set_size, max_set_size) |
limma |
Results list from the |
gene_p_val_cutoff |
Significant p-value to filter the top genes fold change by |
converted |
Return value from the |
idep_data |
List of data files from the database, returned from
|
pathway_p_val_cutoff |
Significant p-value to determine enriched pathways |
n_pathway_show |
Number of pathways to return in final result |
absolute_fold |
TRUE/FALSE to use the absolute value of the fold change |
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()
,
gage_data()
,
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()
,
remove_pathway_id()
,
remove_pathway_id_second()
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