Description Usage Arguments Value Examples
Module detection for the results from a nb_mcupgma call
1 2 3 |
trees |
List of trees, where one tree is a list of ids and rows |
datan |
Data frame were rows correspond to samples and columns to features. |
forest |
Raw dendrogram-matrix as generated by the nb_mcupgma function. |
min_cluster_size |
Integer. The minimum number of features in one module. |
ME_diss_thres |
Numeric. Module Eigengene Dissimilarity Threshold for merging close modules. |
qc_plot |
Logical. Should plots be created? |
n_pc |
Number of principal components and variance explained entries to be calculated. The number of returned variance explained entries is currently ‘min(n_pc,10)’. If given ‘n_pc’ is greater than 10, a warning is issued. |
robust_PCs |
Should PCA be calculated on ranked data (Spearman PCA)? Rotations will not correspond to original data if this is applied. |
nb_min_varExpl |
Minimum proportion of variance explained for returned module eigengenes. The number of PCs is capped at n_pc. |
method |
A character string specifying the method to be used for correlation coefficients. |
List
1 2 3 4 5 6 7 8 9 10 11 12 13 | data('tcga_aml_meth_rna_chr18', package='netboost')
cores <- as.integer(getOption('mc.cores', 2))
datan <- as.data.frame(scale(tcga_aml_meth_rna_chr18, center=TRUE,
scale=TRUE))
filter <- nb_filter(datan=datan, stepno=20L, until=0L, progress=1000L,
cores=cores,mode=2L)
dist <- nb_dist(datan=datan, filter=filter, soft_power=3L, cores=cores)
max_singleton = dim(tcga_aml_meth_rna_chr18)[2]
forest <- nb_mcupgma(filter=filter, dist=dist, max_singleton=max_singleton,
cores=cores)
trees <- tree_search(forest)
results <- cut_trees(trees=trees,datan=datan, forest=forest,
min_cluster_size=10L, ME_diss_thres=0.25, qc_plot=TRUE)
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