Description Usage Arguments Details Value Author(s) References
View source: R/clique_sum_exact.R
An implementation of the clique-based disease module inference method proposed by Barrenäs et al.
1 2 3 | clique_sum_exact(MODifieR_input, db, clique_significance = 0.01,
deg_cutoff = 0.05, min_clique_size = 5, min_deg_in_clique = 3,
multiple_cores = T, n_cores = 4, dataset_name = NULL)
|
MODifieR_input |
A MODifieR input object produced by one of the |
db |
A clique database created by |
clique_significance |
p-value for cliques to be considered significant |
deg_cutoff |
p-value cutoff for differentialy expressed genes |
min_clique_size |
Minimal size for cliques |
min_deg_in_clique |
Minimum number of DEGs to be present in a clique |
multiple_cores |
Parallel process using multiple cores? |
n_cores |
Number of cores to use |
dataset_name |
Optional name for the input object that will be stored in the settings object. Default is the variable name of the input object |
Clique_sum_exact finds cliques of at least size min_clique_size
that are
significantly enriched with DEGs.
The union of maximal cliques with a Fisher-exact test p-value below clique_significance
and at
least min_deg_in_clique
is the final disease module.
clique_sum_exact returns an object of class "MODifieR_module" with subclass "Clique_Sum_exact". This object is a named list containing the following components:
module_genes |
A character vector containing the genes in the final module |
settings |
A named list containing the parameters used in generating the object |
Dirk de Weerd
Barrenäs F, Chavali S, Alves AC, et al. Highly interconnected genes in disease-specific networks are enriched for disease-associated polymorphisms. Genome Biology. 2012;13(6):R46. doi:10.1186/gb-2012-13-6-r46.
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