All examples in this section will be done with the the aCML dataset as reference.

0.1 Summary report for a dataset and boolean queries

We use the function view to get a short summary of a dataset that we loaded in TRONCO; this function reports on the number of samples and events, plus some meta information that could be displayed graphically.

view(aCML)
## Description: CAPRI - Bionformatics aCML data.
## -- TRONCO Dataset: n=64, m=31, |G|=23, patterns=0.
## Events (types): Ins/Del, Missense point, Nonsense Ins/Del, Nonsense point.
## Colors (plot): #7FC97F, #4483B0, #FDC086, #fab3d8.
## Events (5 shown):
##   gene 4 : Ins/Del TET2
##   gene 5 : Ins/Del EZH2
##   gene 6 : Ins/Del CBL
##   gene 7 : Ins/Del ASXL1
##   gene 29 : Missense point SETBP1
## Genotypes (5 shown):

0.2 Creating views with the as functions

Several functions are available to create views over a dataset, with a set of parameter which can constraint the view – as in the SELECT/JOIN approaches in databases. In the following examples we show their execution with the default parameters, but shorten their output to make this document readable.

The main as functions are here documented. as.genotypes, that we can use to get the matrix of genotypes that we imported.

as.genotypes(aCML)[1:10,5:10]
##            gene 29 gene 30 gene 31 gene 32 gene 33 gene 34
## patient 1        1       0       0       0       0       0
## patient 2        1       0       0       0       0       1
## patient 3        1       1       0       0       0       0
## patient 4        1       0       0       0       0       1
## patient 5        1       0       0       0       0       0
## patient 6        1       0       0       0       0       0
## patient 7        1       0       0       0       0       0
## patient 8        1       0       0       0       0       0
## patient 9        1       0       0       0       0       0
## patient 10       1       0       0       0       0       0

Differently, as.events and as.events.in.samples, that show tables with the events that we are processing in all dataset or in a specific sample that we want to examine.

as.events(aCML)[1:5, ]
##         type             event   
## gene 4  "Ins/Del"        "TET2"  
## gene 5  "Ins/Del"        "EZH2"  
## gene 6  "Ins/Del"        "CBL"   
## gene 7  "Ins/Del"        "ASXL1" 
## gene 29 "Missense point" "SETBP1"
as.events.in.sample(aCML, sample = 'patient 2')
##         type             event   
## gene 29 "Missense point" "SETBP1"
## gene 34 "Missense point" "CBL"   
## gene 91 "Nonsense point" "ASXL1"

Concerning genes, as.genes shows the mnemonic names of the genes (or chromosomes, cytobands, etc.) that we included in our dataset.

as.genes(aCML)[1:8]
## [1] "TET2"   "EZH2"   "CBL"    "ASXL1"  "SETBP1" "NRAS"   "KRAS"   "IDH2"

And as.types shows the types of alterations (e.g., mutations, amplifications, etc.) that we have find in our dataset, and function as.colors shows the list of the colors which are associated to each type.

as.types(aCML)
## [1] "Ins/Del"          "Missense point"   "Nonsense Ins/Del" "Nonsense point"
as.colors(aCML)
##          Ins/Del   Missense point Nonsense Ins/Del   Nonsense point 
##        "#7FC97F"        "#4483B0"        "#FDC086"        "#fab3d8"

A function as.gene can be used to display the alterations of a specific gene across the samples

head(as.gene(aCML, genes='SETBP1'))
##           Missense point SETBP1
## patient 1                     1
## patient 2                     1
## patient 3                     1
## patient 4                     1
## patient 5                     1
## patient 6                     1

Views over samples can be created as well. as.samples and which.samples list all the samples in the data, or return a list of samples that harbour a certain alteration. The former is

as.samples(aCML)[1:10]
##  [1] "patient 1"  "patient 2"  "patient 3"  "patient 4"  "patient 5" 
##  [6] "patient 6"  "patient 7"  "patient 8"  "patient 9"  "patient 10"

and the latter is

which.samples(aCML, gene='TET2', type='Nonsense point')
## [1] "patient 12" "patient 13" "patient 26" "patient 29" "patient 40"
## [6] "patient 57" "patient 62"

A slightly different function, which manipulates the data, is as.alterations, which transforms a dataset with events of different type to events of a unique type, labeled Alteration.

dataset = as.alterations(aCML)
## *** Aggregating events of type(s) { Ins/Del, Missense point, Nonsense Ins/Del, Nonsense point }
## in a unique event with label " Alteration ".
## Dropping event types Ins/Del, Missense point, Nonsense Ins/Del, Nonsense point for 23 genes.
## .......................
## *** Binding events for 2 datasets.
view(dataset)
## -- TRONCO Dataset: n=64, m=23, |G|=23, patterns=0.
## Events (types): Alteration.
## Colors (plot): khaki.
## Events (5 shown):
##   G1 : Alteration TET2
##   G2 : Alteration EZH2
##   G3 : Alteration CBL
##   G4 : Alteration ASXL1
##   G5 : Alteration SETBP1
## Genotypes (5 shown):

When samples are enriched with stage information function as.stages can be used to create a view over such table. Views over patterns can be created as well – see Model Inference with CAPRI.

0.3 Dataset size

A set of functions allow to get the number of genes, events, samples, types and patterns in a dataset.

ngenes(aCML)
## [1] 23
nevents(aCML)
## [1] 31
nsamples(aCML)
## [1] 64
ntypes(aCML)
## [1] 4
npatterns(aCML)
## [1] 0

0.4 Oncoprints

Oncoprints are the most effective data-visualization functions in TRONCO. These are heatmaps where rows represent variants, and columns samples (the reverse of the input format required by TRONCO), and are annotated and displayed/sorted to enhance which samples have which mutations etc.

By default oncoprint will try to sort samples and events to enhance exclusivity patterns among the events.

oncoprint(aCML)
## *** Oncoprint for "CAPRI - Bionformatics aCML data"
## with attributes: stage = FALSE, hits = TRUE
## Sorting samples ordering to enhance exclusivity patterns.
## Setting automatic row font (exponential scaling): 8.1