D a t a Vi s u a l i z a t i o n : N i c e B ox p lo t s, Vi o lo n a n ...€¦ · ## PRAD-counts...

11/15/2017 Data Visualization: Nice Boxplots, Violon and density plots with ggpubr package! (1)

file://localhost/Users/dhafermalouche/Documents/Teaching/AdvancedR/visu_genom_data.html#(1) 1/110

Data Visualization: Nice Boxplots,Violon and density plots with ggpubr

package!Dhafer Malouche

http://dhafermalouche.net

http://dhafermalouche.net/



Why this presentation?Presenting nice tools for Data Visualization: Boxplots, Violin plotsand density plots

Application on a Large data: Genomic Data.



OutlineInstalling R packages and data

Preparing Data

Boxplots

Violin plots

Density plots



Installing R packages and data



TCGA dataThe Cancer Genome Atlas (TCGA) data is a publicly available datacontaining clinical and genomic data across 33 cancer types.

These data include gene expression, CNV profiling, SNPgenotyping, DNA methylation, miRNA profiling, exomesequencing, and other types of data.

All the data is available in the RTCGA R package, by MarcinKosinski and Przemyslaw Biecek,



TCGA dataThe following R code installs the core RTCGA package as well as theclinical and mRNA gene expression data packages.

1. Load the bioconductor installer.

> source("https://bioconductor.org/biocLite.R")

> biocLite("RTCGA")

2. Install the main RTCGA package

> library(RTCGA)

> installTCGA("RTCGA.mRNA")

> library(RTCGA.mRNA) # Run this on R not in RStudio

## Welcome to the RTCGA (version: 1.4.0).



Genomic Data> library(RTCGA)

> # Each cell is a data.frame

> # and it represents the number of obs.

> infoTCGA()



Genomic Data## Cohort BCR Clinical CN LowP Methylation mRNA mRNASeq ## ACC-counts ACC 92 92 90 0 80 0 79 ## BLCA-counts BLCA 412 412 410 112 412 0 408 ## BRCA-counts BRCA 1098 1097 1089 19 1097 526 1093 ## CESC-counts CESC 307 307 295 50 307 0 304 ## CHOL-counts CHOL 51 45 36 0 36 0 36 ## COAD-counts COAD 460 458 451 69 457 153 457 ## COADREAD-counts COADREAD 631 629 616 104 622 222 623 ## DLBC-counts DLBC 58 48 48 0 48 0 48 ## ESCA-counts ESCA 185 185 184 51 185 0 184 ## FPPP-counts FPPP 38 38 0 0 0 0 0 ## GBM-counts GBM 613 595 577 0 420 540 160 ## GBMLGG-counts GBMLGG 1129 1110 1090 52 936 567 676 ## HNSC-counts HNSC 528 528 522 108 528 0 520 ## KICH-counts KICH 113 113 66 0 66 0 66 ## KIPAN-counts KIPAN 973 941 883 0 892 88 889 ## KIRC-counts KIRC 537 537 528 0 535 72 533 ## KIRP-counts KIRP 323 291 289 0 291 16 290 ## LAML-counts LAML 200 200 197 0 194 0 179 ## LGG-counts LGG 516 515 513 52 516 27 516 ## LIHC-counts LIHC 377 377 370 0 377 0 371 ## LUAD-counts LUAD 585 522 516 120 578 32 515 ## LUSC-counts LUSC 504 504 501 0 503 154 501 ## MESO-counts MESO 87 87 87 0 87 0 87 ## OV-counts OV 602 591 586 0 594 574 304 ## PAAD-counts PAAD 185 185 184 0 184 0 178 ## PCPG-counts PCPG 179 179 175 0 179 0 179 ## PRAD-counts PRAD 499 499 492 115 498 0 497 ## READ-counts READ 171 171 165 35 165 69 166 ## SARC-counts SARC 261 261 257 0 261 0 259



## SKCM-counts SKCM 470 470 469 118 470 0 469 ## STAD-counts STAD 443 443 442 107 443 0 415 ## STES-counts STES 628 628 626 158 628 0 599 ## TGCT-counts TGCT 150 134 150 0 150 0 150 ## THCA-counts THCA 503 503 499 98 503 0 501 ## THYM-counts THYM 124 124 123 0 124 0 120 ## UCEC-counts UCEC 560 548 540 106 547 54 545 ## UCS-counts UCS 57 57 56 0 57 0 57 ## UVM-counts UVM 80 80 80 51 80 0 80 ## miR miRSeq RPPA MAF rawMAF ## ACC-counts 0 80 46 90 0 ## BLCA-counts 0 409 344 130 395 ## BRCA-counts 0 1078 887 977 0 ## CESC-counts 0 307 173 194 0 ## CHOL-counts 0 36 30 35 0 ## COAD-counts 0 406 360 154 367 ## COADREAD-counts 0 549 491 223 489 ## DLBC-counts 0 47 33 48 0 ## ESCA-counts 0 184 126 185 0 ## FPPP-counts 0 23 0 0 0 ## GBM-counts 565 0 238 290 290 ## GBMLGG-counts 565 512 668 576 806 ## HNSC-counts 0 523 212 279 510 ## KICH-counts 0 66 63 66 66 ## KIPAN-counts 0 873 756 644 799 ## KIRC-counts 0 516 478 417 451 ## KIRP-counts 0 291 215 161 282 ## LAML-counts 0 188 0 197 0 ## LGG-counts 0 512 430 286 516 ## LIHC-counts 0 372 63 198 373 ## LUAD-counts 0 513 365 230 542 ## LUSC-counts 0 478 328 178 0 ## MESO-counts 0 87 63 0 0 ## OV-counts 570 453 426 316 469 ## PAAD-counts 0 178 123 150 184



## PCPG-counts 0 179 80 179 0 ## PRAD-counts 0 494 352 332 498 ## READ-counts 0 143 131 69 122 ## SARC-counts 0 259 223 247 0 ## SKCM-counts 0 448 353 343 366 ## STAD-counts 0 436 357 289 395 ## STES-counts 0 620 483 474 395 ## TGCT-counts 0 150 118 149 0 ## THCA-counts 0 502 222 402 496 ## THYM-counts 0 124 90 123 0 ## UCEC-counts 0 538 440 248 0 ## UCS-counts 0 56 48 57 0 ## UVM-counts 0 80 12 80 0



Merging data setsWe will extract the mRNA expression for five genes of interest

GATA3, PTEN, XBP1, ESR1 and MUC1

from 3 different data sets:

Breast invasive carcinoma (BRCA),

Ovarian serous cystadenocarcinoma (OV) and

Lung squamous cell carcinoma (LUSC)



Merging data sets> expr <- expressionsTCGA(BRCA.mRNA, OV.mRNA, LUSC.mRNA,

+ extract.cols = c("GATA3",

+ "PTEN", "XBP1",

+ "ESR1", "MUC1"))



Merging data sets> dim(expr)

## [1] 1305 7

> colnames(expr)

## [1] "bcr_patient_barcode" "dataset" "GATA3" ## [4] "PTEN" "XBP1" "ESR1" ## [7] "MUC1"



Merging data sets> expr

## # A tibble: 1,305 x 7 ## bcr_patient_barcode datas… GATA3 PTEN XBP1 ESR1 MUC1 ## <chr> <chr> <dbl> <dbl> <dbl> <dbl> <dbl> ## 1 TCGA-A1-A0SD-01A-11R-A115-07 BRCA.… 2.87 1.36 2.98 3.08 1.65 ## 2 TCGA-A1-A0SE-01A-11R-A084-07 BRCA.… 2.17 0.428 2.55 2.39 3.08 ## 3 TCGA-A1-A0SH-01A-11R-A084-07 BRCA.… 1.32 1.31 3.02 0.791 2.99 ## 4 TCGA-A1-A0SJ-01A-11R-A084-07 BRCA.… 1.84 0.810 3.13 2.50 -1.92 ## 5 TCGA-A1-A0SK-01A-12R-A084-07 BRCA.… -6.03 0.251 -1.45 -4.86 -1.17 ## 6 TCGA-A1-A0SM-01A-11R-A084-07 BRCA.… 1.80 1.31 4.04 2.80 3.53 ## 7 TCGA-A1-A0SO-01A-22R-A084-07 BRCA.… -4.88 -0.237 -0.725 -4.49 -1.46 ## 8 TCGA-A1-A0SP-01A-11R-A084-07 BRCA.… -3.14 -1.24 -1.19 -1.63 -0.987 ## 9 TCGA-A2-A04N-01A-11R-A115-07 BRCA.… 2.03 1.21 2.28 4.12 0.668 ## 10 TCGA-A2-A04P-01A-31R-A034-07 BRCA.… -0.293 0.288 -1.61 0.473 0.0115 ## # ... with 1,295 more rows



Preparing the data



Preparing the dataTo display the number of sample in each data set:

> nb_samples <- table(expr$dataset)

> nb_samples

## ## BRCA.mRNA LUSC.mRNA OV.mRNA ## 590 154 561

We simplify data set names by removing the “mRNA” tag.

> expr$dataset <- gsub(pattern = ".mRNA",

+ replacement = "", expr$dataset)



Preparing the dataWe simplify also the patients’ barcode column. The following R codewill change the barcodes into BRCA1, BRCA2, …, OV1, OV2, …., etc

> expr$bcr_patient_barcode <- paste0(expr$dataset,

+ c(1:590, 1:561, 1:154))



Preparing the data> expr

## # A tibble: 1,305 x 7 ## bcr_patient_barcode dataset GATA3 PTEN XBP1 ESR1 MUC1 ## <chr> <chr> <dbl> <dbl> <dbl> <dbl> <dbl> ## 1 BRCA1 BRCA 2.87 1.36 2.98 3.08 1.65 ## 2 BRCA2 BRCA 2.17 0.428 2.55 2.39 3.08 ## 3 BRCA3 BRCA 1.32 1.31 3.02 0.791 2.99 ## 4 BRCA4 BRCA 1.84 0.810 3.13 2.50 -1.92 ## 5 BRCA5 BRCA -6.03 0.251 -1.45 -4.86 -1.17 ## 6 BRCA6 BRCA 1.80 1.31 4.04 2.80 3.53 ## 7 BRCA7 BRCA -4.88 -0.237 -0.725 -4.49 -1.46 ## 8 BRCA8 BRCA -3.14 -1.24 -1.19 -1.63 -0.987 ## 9 BRCA9 BRCA 2.03 1.21 2.28 4.12 0.668 ## 10 BRCA10 BRCA -0.293 0.288 -1.61 0.473 0.0115 ## # ... with 1,295 more rows



Boxplots



Installing ggpubr package

> if(!require(devtools)) install.packages("devtools")

> devtools::install_github("kassambara/ggpubr")



Load ggpubr:> library(ggpubr)

## Loading required package: ggplot2

## Loading required package: magrittr



First boxplotCreate a box plot of a gene expression profile, colored by groups (heredataset/cancer type)



GATA3> ggboxplot(expr, x = "dataset", y = "GATA3",

+ title = "GATA3", ylab = "Expression",

+ color = "dataset", palette = "jco")



GATA3



PTEN> ggboxplot(expr, x = "dataset", y = "GATA3",

+ title = "PTEN", ylab = "Expression",




PTEN



Create a list of boxplots



Create a list of boxplots> p <- ggboxplot(expr, x = "dataset",

+ y = c("GATA3", "PTEN", "XBP1"),

+ title = c("GATA3", "PTEN", "XBP1"),

+ ylab = "Expression",




View GATA3> p$GATA3



View GATA3



View PTEN> p$PTEN



View PTEN



View XBP1> p$XBP1



View XBP1



Adding p-values> my_comparisons <- list(c("BRCA", "OV"), c("OV", "LUSC"))

> ggboxplot(expr, x = "dataset", y = "GATA3",


+ color = "dataset", palette = "jco")+

+ stat_compare_means(comparisons = my_comparisons)



Adding p-values



Other comparisons> my_comparisons <- list(c("BRCA", "OV"),

+ c("OV", "LUSC"),

+ c("BRCA","LUSC"))



+ color = "dataset", palette = "jco")+

+ stat_compare_means(comparisons = my_comparisons)



Other comparisons



Comparing different groups> comp_data=compare_means(c(GATA3, PTEN, XBP1) ~ dataset, data = expr)

> comp_data

## # A tibble: 9 x 8 ## .y. group1 group2 p p.adj p.fo… p.si… meth… ## <fctr> <chr> <chr> <dbl> <dbl> <chr> <chr> <chr> ## 1 GATA3 BRCA OV 1.11e⁻¹⁷⁷ 3.34e⁻¹⁷⁷ < 2e… **** Wilc… ## 2 GATA3 BRCA LUSC 6.68e⁻ ⁷³ 1.34e⁻ ⁷² < 2e… **** Wilc… ## 3 GATA3 OV LUSC 2.97e⁻ ⁸ 2.97e⁻ ⁸ 3.0e… **** Wilc… ## 4 PTEN BRCA OV 6.79e⁻ ⁵ 6.79e⁻ ⁵ 6.8e… **** Wilc… ## 5 PTEN BRCA LUSC 1.04e⁻ ¹⁶ 3.13e⁻ ¹⁶ < 2e… **** Wilc… ## 6 PTEN OV LUSC 1.28e⁻ ⁷ 2.56e⁻ ⁷ 1.3e… **** Wilc… ## 7 XBP1 BRCA OV 2.55e⁻¹²³ 7.65e⁻¹²³ < 2e… **** Wilc… ## 8 XBP1 BRCA LUSC 1.95e⁻ ⁴² 3.90e⁻ ⁴² < 2e… **** Wilc… ## 9 XBP1 OV LUSC 4.24e⁻ ¹¹ 4.24e⁻ ¹¹ 4.2e… **** Wilc…



More optionsSelect items (here cancer types) to display.



+ color = "dataset", palette = "jco",

+ select = c("BRCA", "OV"))



More options



More optionsRemove items (here cancer types) to display.




+ remove = "BRCA")



More options



More optionsChange the order of the dataset on x axis




+ order = c("LUSC", "OV", "BRCA"))



More options



More optionsCreate horizontal plots




+ rotate = TRUE)



More options



Multi-plots in the same figureCombine the three gene expression plots into a multi-panel plot, use theargument combine = TRUE:

> ggboxplot(expr, x = "dataset",

+ y = c("GATA3", "PTEN", "XBP1"),

+ combine = TRUE,





Multi-plots in the same figure



Multi-plots in the same figureMerge the 3 plots using the argument merge = TRUE:


+ y = c("GATA3", "PTEN", "XBP1"),

+ merge = TRUE,


+ palette = "jco")



Multi-plots in the same figureMerge the 3 plots using the argument merge = "asis":


+ y = c("GATA3", "PTEN", "XBP1"),

+ merge = "asis",


+ palette = "jco")



Multi-plots in the same figureThe y variables (i.e.: genes) become x tick labels and the x variable (i.e.:dataset) becomes the grouping variable. To do this, use the argumentmerge = “flip”:



Multi-plots in the same figure> ggboxplot(expr, x = "dataset",

+ y = c("GATA3", "PTEN", "XBP1"),

+ merge = "flip",


+ palette = "jco")



Adding decorationsAdd jittered points on the boxplot.


+ y = c("GATA3", "PTEN", "XBP1"),

+ combine = TRUE,



+ add = "jitter", # Add jittered points

+ add.params = list(size = 0.1, jitter = 0.2) # Point size and the amount of jittering

+ )



Adding decorations



Adding decorationsAdd and adjust a dotplot.


+ y = c("GATA3", "PTEN", "XBP1"),

+ combine = TRUE,



+ add = "dotplot", # Add dotplot

+ add.params = list(binwidth = 0.1, dotsize = 0.3)

+ )



Adding decorations



Adding labelsWe can label the boxplot by showing the names of samples withthe top highest or lowest values.

You can use the following arguments:

label: the name of the column containing point labels.

label.select: can be of two formats:

a character vector specifying some labels to show.

a list containing one or the combination of the following components: top.upand top.down: to display the labels of the top up/down points.

n



Adding labelsExample,

label.select = list(top.up = 10, top.down = 4) or

label.select = list(criteria = “y > 3.9 & y < 5 & x %in% c(‘BRCA’,‘OV’)”)



Adding labels> ggboxplot(expr, x = "dataset",

+ y = c("GATA3", "PTEN", "XBP1"),

+ combine = TRUE,



+ add = "jitter", # Add jittered points

+ add.params = list(size = 0.1, jitter = 0.2), # Point size and the amount of jittering

+ label = "bcr_patient_barcode", # column containing point labels

+ label.select = list(top.up = 2, top.down = 2),# Select some labels to display

+ font.label = list(size = 9, face = "italic"), # label font

+ repel = TRUE # Avoid label text overplotting

+ )



Adding labels



Adding labels> label.select.criteria <- list(criteria = "`y` > 3.9 & `x` %in% c('BRCA', 'OV')")


+ y = c("GATA3", "PTEN", "XBP1"),

+ combine = TRUE,



+ label = "bcr_patient_barcode", # column containing point labels

+ label.select = label.select.criteria, # Select some labels to display

+ font.label = list(size = 9, face = "italic"), # label font

+ repel = TRUE # Avoid label text overplotting

+ )



Adding labels



Violin plots



Violin + Boxplot> ggviolin(expr, x = "dataset",

+ y = c("GATA3", "PTEN", "XBP1"),

+ combine = TRUE,



+ add = "boxplot")



Violin + Boxplot



Computing descriptive statistics> library(reshape)

> dt=as.data.frame(expr[,-1])

> expr2=melt(dt)

## Using dataset as id variables

> head(expr2,2)

## dataset variable value ## 1 BRCA GATA3 2.87050 ## 2 BRCA GATA3 2.16625



Computing descriptive statistics> res<-desc_statby(expr2,measure.var = "value",grps=c("dataset","variable"))

> res

## dataset variable length min max median mean ## 1 BRCA GATA3 590 -6.025250 3.930000 1.6763750 1.1035732 ## 2 BRCA PTEN 590 -2.398357 2.802786 0.8123929 0.7486928 ## 3 BRCA XBP1 590 -2.438250 4.736750 2.1194167 1.7498139 ## 4 BRCA ESR1 590 -4.860667 6.110833 3.0645833 2.2982359 ## 5 BRCA MUC1 590 -2.793875 4.280500 2.2476875 1.8527130 ## 6 LUSC GATA3 154 -5.059500 1.196625 -3.9270625 -3.7584818 ## 7 LUSC PTEN 154 -1.935429 1.472357 0.3048571 0.2516035 ## 8 LUSC XBP1 154 -2.291083 2.194083 -0.4241250 -0.2916250 ## 9 LUSC ESR1 154 -5.195417 0.421750 -3.0606250 -2.9925693 ## 10 LUSC MUC1 154 -1.814250 3.240375 0.6474375 0.5622597 ## 11 OV GATA3 561 -5.963250 1.395875 -4.2500000 -4.2256808 ## 12 OV PTEN 561 -2.750357 2.727500 0.6530714 0.5723408 ## 13 OV XBP1 561 -3.187750 1.910583 -0.8346667 -0.8727874 ## 14 OV ESR1 561 -5.033167 4.334583 1.6151667 1.4866153 ## 15 OV MUC1 561 -3.323375 4.561875 2.4697500 2.2671916 ## iqr mad sd se ci range ## 1 2.0183125 1.1917324 1.8002158 0.07411371 0.14555931 9.955250 ## 2 0.7508929 0.5542806 0.6917991 0.02848092 0.05593652 5.201143 ## 3 1.7493750 1.1950992 1.5070681 0.06204501 0.12185639 7.175000 ## 4 3.1700833 1.9828540 2.6218080 0.10793813 0.21199046 10.971500 ## 5 2.0145625 1.4114352 1.4999340 0.06175131 0.12127955 7.074375 ## 6 1.0329063 0.7490836 0.9132301 0.07359018 0.14538404 6.256125 ## 7 0.8792321 0.6602865 0.6550587 0.05278614 0.10428378 3.407786 ## 8 0.9772500 0.7592765 0.8248771 0.06647049 0.13131846 4.485167



## 9 1.0367708 0.7768206 1.0459820 0.08428763 0.16651783 5.617167 ## 10 1.8160313 1.2928272 1.1499654 0.09266685 0.18307173 5.054625 ## 11 0.8773750 0.6484522 0.7335973 0.03097250 0.06083647 7.359125 ## 12 0.9690714 0.7268976 0.7741196 0.03268335 0.06419694 5.477857 ## 13 1.3240000 0.9892648 0.9220309 0.03892817 0.07646308 5.098333 ## 14 1.2080000 0.8978378 1.2030989 0.05079487 0.09977176 9.367750 ## 15 1.1295000 0.8280321 1.0288869 0.04343964 0.08532454 7.885250 ## cv var ## 1 1.6312609 3.2407769 ## 2 0.9240093 0.4785860 ## 3 0.8612734 2.2712544 ## 4 1.1407915 6.8738772 ## 5 0.8095879 2.2498020 ## 6 -0.2429784 0.8339891 ## 7 2.6035355 0.4291020 ## 8 -2.8285542 0.6804223 ## 9 -0.3495264 1.0940784 ## 10 2.0452565 1.3224203 ## 11 -0.1736045 0.5381650 ## 12 1.3525501 0.5992611 ## 13 -1.0564209 0.8501409 ## 14 0.8092873 1.4474469 ## 15 0.4538156 1.0586083



Statistics on the violin plot> ggviolin(expr, x = "dataset",

+ y = c("GATA3", "PTEN", "XBP1"),

+ combine = TRUE,



+ add = "mean_se")



Statistics on the violin plot



Adding quantiles> ggviolin(expr, x = "dataset",

+ y = c("GATA3", "PTEN", "XBP1"),

+ combine = TRUE, draw_quantiles = c(.025,.5,.75,.975),



+ add = "boxplot")



Adding quantiles



Density plotsTo visualize the distribution as a density plot,

> ggdensity(expr,

+ x = c("GATA3", "PTEN", "XBP1"),

+ y = "..density..",

+ combine = TRUE, # Combine the 3 plots

+ xlab = "Expression",

+ add = "median", # Add median line.

+ rug = TRUE # Add marginal rug

+ )



Density plots



Density plotsChange color and fill by dataset

> ggdensity(expr,

+ x = c("GATA3", "PTEN", "XBP1"),

+ y = "..density..",

+ combine = TRUE, # Combine the 3 plots



+ rug = TRUE, # Add marginal rug

+ color = "dataset",

+ fill = "dataset",

+ palette = "jco"

+ )



Density plots



Density plotsMerging all the plots in one figure

> ggdensity(expr,

+ x = c("GATA3", "PTEN", "XBP1"),

+ y = "..count..",

+ color = ".x.", fill = ".x.", # color and fill by x variables

+ merge = TRUE, # Merge the 3 plots



+ rug = TRUE , # Add marginal rug

+ palette = "jco" # Change color palette

+ )



Density plotsMerging all the plots in one figure



Density plotsFacet by dataset

> ggdensity(expr,

+ x = c("GATA3", "PTEN", "XBP1"),

+ y = "..count..",

+ color = ".x.", fill = ".x.",

+ facet.by = "dataset", # Split by "dataset" into multi-panel

+ merge = TRUE, # Merge the 3 plots



+ rug = TRUE , # Add marginal rug

+ palette = "jco" # Change color palette

+ )



Density plots

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