| visualizeClusters | R Documentation |
Visualize the clusters according to pvalue thresholds
visualizeClusters( dat, clust_model, adjusted_pValues, FDR_th = NULL, ttl = "", subttl = "" )
dat |
the standardize data returned by the function [checkClusterability()] |
clust_model |
the clustering model obtained with dat. |
adjusted_pValues |
vector of the adjusted pvalues obtained for each protein with a 1-way ANOVA (for example obtained with the function [wrapperClassic1wayAnova()]). |
FDR_th |
the thresholds of FDR pvalues for the coloring of the profiles. The default (NULL) creates 4 thresholds: 0.001, 0.005, 0.01, 0.05 For the sake of readability, a maximum of 4 values can be specified. |
ttl |
title for the plot. |
subttl |
subtitle for the plot. |
a ggplot object
Helene Borges
library(dplyr)
utils::data(Exp1_R25_prot, package='DAPARdata')
obj <- Exp1_R25_prot[1:1000]
level <- obj@experimentData@other$typeOfData
metacell.mask <- match.metacell(GetMetacell(obj), 'missing', level)
indices <- GetIndices_WholeMatrix(metacell.mask, op='>=', th=1)
obj <- MetaCellFiltering(obj, indices, cmd='delete')
expR25_ttest <- compute_t_tests(obj$new)
averaged_means <- averageIntensities(obj$new)
only_means <- dplyr::select_if(averaged_means, is.numeric)
only_features <- dplyr::select_if(averaged_means, is.character)
means <- purrr::map(purrr::array_branch(as.matrix(only_means), 1),mean)
centered <- only_means - unlist(means)
centered_means <- dplyr::bind_cols(feature = dplyr::as_tibble(only_features),
dplyr::as_tibble(centered))
difference <- only_means[,1] - only_means[,2]
clusters <- as.data.frame(difference) %>%
dplyr::mutate(cluster = dplyr::if_else(difference > 0, 1,2))
vizu <- visualizeClusters(dat = centered_means,
clust_model = as.factor(clusters$cluster),
adjusted_pValues = expR25_ttest$P_Value$`25fmol_vs_10fmol_pval`,
FDR_th = c(0.001,0.005,0.01,0.05),
ttl = "Clustering of protein profiles")
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