Function creates heatmaps (geom_tile) for TCGA Datasets.
heatmapTCGA(data, x, y, fill, legend.title = "Expression", legend = "right", title = "Heatmap of expression", facet.names = NULL, tile.size = 0.1, tile.color = "white", ...)
heatmapTCGA
uses scale_fill_viridis from viridis package which is a port of the new
matplotlib
color maps (viridis - the default -, magma
, plasma
and inferno
) to R
.
matplotlib
http://matplotlib.org/ is a popular plotting library for python
.
These color maps are designed in such a way that they will analytically be perfectly perceptually-uniform,
both in regular form and also when converted to black-and-white.
They are also designed to be perceived by readers with the most common form of color blindness.
If you have any problems, issues or think that something is missing or is not clear please post an issue on https://github.com/RTCGA/RTCGA/issues.
RTCGA website http://rtcga.github.io/RTCGA/articles/Visualizations.html.
Other RTCGA: RTCGA-package
,
boxplotTCGA
, checkTCGA
,
convertTCGA
, createTCGA
,
datasetsTCGA
, downloadTCGA
,
expressionsTCGA
, infoTCGA
,
installTCGA
, kmTCGA
,
mutationsTCGA
, pcaTCGA
,
readTCGA
, survivalTCGA
,
theme_RTCGA
library(RTCGA.rnaseq) # perfrom plot library(dplyr) expressionsTCGA(ACC.rnaseq, BLCA.rnaseq, BRCA.rnaseq, OV.rnaseq, extract.cols = c("MET|4233", "ZNF500|26048", "ZNF501|115560")) %>% rename(cohort = dataset, MET = `MET|4233`) %>% #cancer samples filter(substr(bcr_patient_barcode, 14, 15) == "01") %>% mutate(MET = cut(MET, round(quantile(MET, probs = seq(0,1,0.25)), -2), include.lowest = TRUE, dig.lab = 5)) -> ACC_BLCA_BRCA_OV.rnaseq ACC_BLCA_BRCA_OV.rnaseq %>% select(-bcr_patient_barcode) %>% group_by(cohort, MET) %>% summarise_each(funs(median)) %>% mutate(ZNF500 = round(`ZNF500|26048`), ZNF501 = round(`ZNF501|115560`)) -> ACC_BLCA_BRCA_OV.rnaseq.medians heatmapTCGA(ACC_BLCA_BRCA_OV.rnaseq.medians, "cohort", "MET", "ZNF500", title = "Heatmap of ZNF500 expression")## facet example library(RTCGA.mutations) library(dplyr) mutationsTCGA(BRCA.mutations, OV.mutations, ACC.mutations, BLCA.mutations) %>% filter(Hugo_Symbol == 'TP53') %>% filter(substr(bcr_patient_barcode, 14, 15) == "01") %>% # cancer tissue mutate(bcr_patient_barcode = substr(bcr_patient_barcode, 1, 12)) -> ACC_BLCA_BRCA_OV.mutations mutationsTCGA(BRCA.mutations, OV.mutations, ACC.mutations, BLCA.mutations) -> ACC_BLCA_BRCA_OV.mutations_all ACC_BLCA_BRCA_OV.rnaseq %>% mutate(bcr_patient_barcode = substr(bcr_patient_barcode, 1, 15)) %>% filter(bcr_patient_barcode %in% substr(ACC_BLCA_BRCA_OV.mutations_all$bcr_patient_barcode, 1, 15)) %>% # took patients for which we had any mutation information # so avoided patients without any information about mutations mutate(bcr_patient_barcode = substr(bcr_patient_barcode, 1, 12)) %>% # strin_length(ACC_BLCA_BRCA_OV.mutations$bcr_patient_barcode) == 12 left_join(ACC_BLCA_BRCA_OV.mutations, by = "bcr_patient_barcode") %>% #joined only with tumor patients mutate(TP53 = ifelse(!is.na(Variant_Classification), "Mut", "WILD")) %>% select(-bcr_patient_barcode, -Variant_Classification, -dataset, -Hugo_Symbol) %>% group_by(cohort, MET, TP53) %>% summarise_each(funs(median)) %>% mutate(ZNF501 = round(`ZNF501|115560`)) -> ACC_BLCA_BRCA_OV.rnaseq_TP53mutations_ZNF501medians heatmapTCGA(ACC_BLCA_BRCA_OV.rnaseq_TP53mutations_ZNF501medians, "cohort", "MET", fill = "ZNF501", facet.names = "TP53", title = "Heatmap of ZNF501 expression")heatmapTCGA(ACC_BLCA_BRCA_OV.rnaseq_TP53mutations_ZNF501medians, "TP53", "MET", fill = "ZNF501", facet.names = "cohort", title = "Heatmap of ZNF501 expression")heatmapTCGA(ACC_BLCA_BRCA_OV.rnaseq_TP53mutations_ZNF501medians, "TP53", "cohort", fill = "ZNF501", facet.names = "MET", title = "Heatmap of ZNF501 expression")