Nothing
## ---- fig.show='hold', message=FALSE, warning=FALSE, eval=FALSE---------------
# ## try http:// if https:// URLs are not supported
# if (!requireNamespace("BiocManager", quietly=TRUE))
# install.packages("BiocManager")
# BiocManager::install("hipathia")
## ---- fig.show='hold', message=FALSE, warning=FALSE---------------------------
library(hipathia)
data("brca")
brca
## ---- echo=FALSE, message=FALSE, warning=FALSE--------------------------------
# library(devtools)
# load_all("~/appl/hipathia/")
## ---- fig.show='hold', message=FALSE, warning=FALSE---------------------------
hhead(assay(brca), 4)
## ---- fig.show='hold', message=FALSE, warning=FALSE---------------------------
colData(brca)
## ---- fig.show='hold', message=FALSE, eval=FALSE------------------------------
# brca <- SummarizedExperiment(assays=SimpleList(raw=brca_data),
# colData=brca_design)
## ---- fig.show='hold'---------------------------------------------------------
data(brca_data)
trans_data <- translate_data(brca_data, "hsa")
## ---- fig.show='hold'---------------------------------------------------------
exp_data <- normalize_data(trans_data)
## ---- fig.show='hold', fig.cap="BRCA data before scaling"---------------------
boxplot(trans_data)
## ---- fig.show='hold', fig.cap="BRCA data after scaling"----------------------
boxplot(exp_data)
## ---- fig.show='hold', fig.cap="BRCA data after a Quantiles normalization"----
exp_data <- normalize_data(trans_data, by_quantiles = TRUE)
boxplot(exp_data)
## ---- fig.show='hold', fig.cap="BRCA data after normalizing by percentil"-----
exp_data <- normalize_data(trans_data, percentil = TRUE)
boxplot(exp_data)
## ---- fig.show='hold', fig.cap="BRCA data after truncating by percentil 0.95"----
exp_data <- normalize_data(trans_data, truncation_percentil = 0.95)
boxplot(exp_data)
## ---- fig.show='hold'---------------------------------------------------------
pathways <- load_pathways(species = "hsa")
## ---- fig.show='hold'---------------------------------------------------------
pathways_only2 <- load_pathways(species = "hsa", pathways_list = c("hsa03320",
"hsa04014"))
## ---- fig.show='hold'---------------------------------------------------------
length(get_pathways_list(pathways))
get_pathways_list(pathways)[1:10]
## ---- fig.show='hold'---------------------------------------------------------
length(get_pathways_list(pathways_only2))
get_pathways_list(pathways_only2)
## ---- fig.show='hold'---------------------------------------------------------
results <- hipathia(exp_data, pathways, decompose = FALSE, verbose=FALSE)
## ---- fig.show='hold'---------------------------------------------------------
results
## ---- fig.show='hold'---------------------------------------------------------
path_vals <- get_paths_data(results, matrix = TRUE)
path_vals <- get_paths_data(results)
hhead(path_vals, 4)
## ---- echo=FALSE, results='asis'----------------------------------------------
tab <- t(sapply(c("hsa", "mmu", "rno"), function(species){
p <- suppressMessages(load_pathways(species))
effs <- sum(sapply(p$pathigraphs, function(pathi) length(
pathi$effector.subgraphs)))
decs <- sum(sapply(p$pathigraphs, function(pathi) length(pathi$subgraphs)))
n <- length(p$pathigraphs)
c(n, effs, decs)
}))
colnames(tab) <- c("Pathways", "Effector subpathways", "Decomposed subpathways")
knitr::kable(tab)
## ---- fig.show='hold'---------------------------------------------------------
uniprot_vals <- quantify_terms(results, pathways, dbannot = "uniprot")
go_vals <- quantify_terms(results, pathways, dbannot = "GO")
## ---- fig.show='hold'---------------------------------------------------------
sample_group <- brca_design[colnames(path_vals),"group"]
comp <- do_wilcoxon(path_vals, sample_group, g1 = "Tumor", g2 = "Normal")
hhead(comp)
## ---- fig.show='hold'---------------------------------------------------------
pathways_summary <- get_pathways_summary(comp, pathways)
head(pathways_summary, 4)
## ---- fig.show='hold'---------------------------------------------------------
ranked_path_vals <- path_vals[order(comp$p.value, decreasing = FALSE),]
pca_model <- do_pca(ranked_path_vals[1:ncol(ranked_path_vals),])
## ---- fig.show='hold', fig.cap="Heatmap plot", fig.small=TRUE-----------------
heatmap_plot(path_vals, group = sample_group)
## ---- fig.show='hold', fig.cap="Heatmap plots with variable clustering", fig.small=TRUE----
heatmap_plot(uniprot_vals, group = sample_group, colors="hipathia",
variable_clust = TRUE)
## ---- fig.show='hold', fig.cap="Different colors of heatmaps: `redgreen`", fig.small=TRUE----
heatmap_plot(go_vals, group = sample_group, colors="redgreen",
variable_clust = TRUE)
## ---- fig.show='hold', fig.cap="PCA plot"-------------------------------------
pca_plot(pca_model, sample_group, legend = TRUE)
## ---- fig.show='hold', fig.cap="PCA plot with 5 random colors"----------------
pca_plot(pca_model, group = rep(1:5, 8), main = "Random types",
legend = TRUE)
## ---- fig.show='hold', fig.cap="Multiple PCA plot with acumulated explained variance"----
multiple_pca_plot(pca_model, sample_group, cex=3, plot_variance = TRUE)
## ---- fig.show='hold', fig.cap= "Pathway comparison plot without node colors"----
pathway_comparison_plot(comp, metaginfo = pathways, pathway = "hsa03320")
## ---- fig.show='hold', fig.cap="Pathway comparison plot with node colors: `classic`"----
colors_de <- node_color_per_de(results, pathways, sample_group, "Tumor",
"Normal")
pathway_comparison_plot(comp, metaginfo = pathways, pathway = "hsa03320",
node_colors = colors_de)
## ---- fig.show='hold', fig.cap="Pathway comparison plot with node colors: `hipathia`"----
colors_de_hipathia <- node_color_per_de(results, pathways, sample_group,
"Tumor", "Normal", colors = "hipathia")
pathway_comparison_plot(comp, metaginfo = pathways, pathway = "hsa03320",
node_colors = colors_de_hipathia, colors = "hipathia")
## ---- fig.show='hold'---------------------------------------------------------
report <- create_report(comp, pathways, "save_noColors")
report_colors <- create_report(comp, pathways, "save_colors",
node_colors = colors_de)
## ---- fig.show='hold'---------------------------------------------------------
visualize_report(report_colors)
## ---- fig.show='hold'---------------------------------------------------------
visualize_report(report, port = 4001)
## ---- fig.show='hold'---------------------------------------------------------
servr::daemon_stop()
## ---- fig.show='hold', eval=FALSE---------------------------------------------
# colors_de_uni <- node_color_per_de(results, pathways, sample_group, "Tumor",
# "Normal", group_by = "uniprot")
# create_report(comp, pathways, "save_colors_uniprot",
# node_colors = colors_de_uni, group_by = "uniprot")
# visualize_report("save_colors_uniprot", port = 4002)
## ---- fig.show='hold'---------------------------------------------------------
servr::daemon_stop()
## ---- echo=TRUE---------------------------------------------------------------
newmgi <- mgi_from_sif(system.file("extdata/SIF_ATT_example",
package = "hipathia"),
spe = "hsa")
## ---- echo=FALSE--------------------------------------------------------------
sif <- read.delim(system.file("extdata/SIF_ATT_example/hsa00.sif",
package = "hipathia"),
header = FALSE, sep = "\t", stringsAsFactors = FALSE)
names(sif) <- NULL
rownames(sif) <- c("", " ", " ", " ")
print(sif)
## ---- echo=FALSE--------------------------------------------------------------
att <- read.delim(system.file("extdata/SIF_ATT_example/hsa00.att",
package = "hipathia"),
header = TRUE, sep = "\t", stringsAsFactors = FALSE)
rownames(att) <- c("", " ", " ", " ", " ")
print(att)
## ---- echo=FALSE--------------------------------------------------------------
nam <- read.delim(system.file("extdata/SIF_ATT_example/name.pathways_hsa.txt",
package = "hipathia"),
header = FALSE, sep = "\t", stringsAsFactors = FALSE)
names(nam) <- NULL
rownames(nam) <- ""
print(nam)
## ---- fig.show='hold', message=FALSE, warning=FALSE---------------------------
class(brca)
hhead(brca, 4)
## ---- fig.show='hold', message=FALSE, warning=FALSE---------------------------
class(assay(brca))
hhead(assay(brca), 4)
## ---- fig.show='hold'---------------------------------------------------------
get_path_names(pathways, c("P-hsa03320-37", "P-hsa04010-15"))
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