plotVar: Plot of Variables

In ajabadi/mixOmics2: Omics Data Integration Project

Description

This function provides variables representation for (regularized) CCA, (sparse) PLS regression, PCA and (sparse) Regularized generalised CCA.

Usage

plotVar(object, comp = NULL, comp.select = comp, plot = TRUE,
  var.names = NULL, blocks = NULL, X.label = NULL, Y.label = NULL,
  Z.label = NULL, abline = TRUE, col, cex, pch, font, cutoff = 0,
  rad.in = 0.5, title = "Correlation Circle Plots", legend = FALSE,
  legend.title = "Block", style = "ggplot2", overlap = TRUE,
  axes.box = "all", label.axes.box = "both")

Arguments

object	object of class inheriting from "rcc", "pls", "plsda", "spls", "splsda", "pca" or "spca".
comp	integer vector of length two. The components that will be used on the horizontal and the vertical axis respectively to project the variables. By default, comp=c(1,2) except when style='3d', comp=c(1:3)
comp.select	for the sparse versions, an input vector indicating the components on which the variables were selected. Only those selected variables are displayed. By default, comp.select=comp
plot	if TRUE (the default) then a plot is produced. If not, the summaries which the plots are based on are returned.
var.names	either a character vector of names for the variables to be plotted, or FALSE for no names. If TRUE, the col names of the first (or second) data matrix is used as names.
blocks	for an object of class "rgcca" or "sgcca", a numerical vector indicating the block variables to display.
X.label	x axis titles.
Y.label	y axis titles.
Z.label	z axis titles (when style = '3d').
abline	should the vertical and horizontal line through the center be plotted? Default set to FALSE
col	character or integer vector of colors for plotted character and symbols, can be of length 2 (one for each data set) or of length (p+q) (i.e. the total number of variables). See Details.
cex	numeric vector of character expansion sizes for the plotted character and symbols, can be of length 2 (one for each data set) or of length (p+q) (i.e. the total number of variables).
pch	plot character. A vector of single characters or integers, can be of length 2 (one for each data set) or of length (p+q) (i.e. the total number of variables). See points for all alternatives.
font	numeric vector of font to be used, can be of length 2 (one for each data set) or of length (p+q) (i.e. the total number of variables). See par for details.
cutoff	numeric between 0 and 1. Variables with correlations below this cutoff in absolute value are not plotted (see Details).
rad.in	numeric between 0 and 1, the radius of the inner circle. Defaults to 0.5.
title	character indicating the title plot.
legend	boolean when more than 3 blocks. Can be a character vector when one or 2 blocks to customize the legend. See examples. Default is FALSE.
legend.title	title of the legend
style	argument to be set to either 'graphics', 'lattice', 'ggplot2' or '3d' for a style of plotting.
overlap	boolean. Whether the variables should be plotted in one single figure. Default is TRUE.
axes.box	for style '3d', argument to be set to either 'axes', 'box', 'bbox' or 'all', defining the shape of the box.
label.axes.box	for style '3d', argument to be set to either 'axes', 'box', 'both', indicating which labels to print.

Details

plotVar produce a "correlation circle", i.e. the correlations between each variable and the selected components are plotted as scatter plot, with concentric circles of radius one et radius given by rad.in. Each point corresponds to a variable. For (regularized) CCA the components correspond to the equiangular vector between X- and Y-variates. For (sparse) PLS regression mode the components correspond to the X-variates. If mode is canonical, the components for X and Y variables correspond to the X- and Y-variates respectively.

For plsda and splsda objects, only the X variables are represented.

For spls and splsda objects, only the X and Y variables selected on dimensions comp are represented.

The arguments col, pch, cex and font can be either vectors of length two or a list with two vector components of length p and q respectively, where p is the number of X-variables and q is the number of Y-variables. In the first case, the first and second component of the vector determine the graphics attributes for the X- and Y-variables respectively. Otherwise, multiple arguments values can be specified so that each point (variable) can be given its own graphic attributes. In this case, the first component of the list correspond to the X attributs and the second component correspond to the Y attributs. Default values exist for this arguments.

Value

A list containing the following components:

x	a vector of coordinates of the variables on the x-axis.
y	a vector of coordinates of the variables on the y-axis.
Block	the data block name each variable belongs to.
names	the name of each variable, matching their coordinates values.

Author(s)

Ignacio González, Kim-Anh Lê Cao, Benoit Gautier, Florian Rohart, Francois Bartolo.

References

González I., Lê Cao K-A., Davis, M.J. and Déjean, S. (2012). Visualising associations between paired 'omics data sets. J. Data Mining 5:19. http://www.biodatamining.org/content/5/1/19/abstract

See Also

cim, network, par and http://www.mixOmics.org for more details.

Examples

## variable representation for objects of class 'rcc'
# ----------------------------------------------------
X <- nutrimouse$lipid
Y <- nutrimouse$gene
nutri.res <- rcc(X, Y, ncomp = 3, lambda1 = 0.064, lambda2 = 0.008)

plotVar(nutri.res) #(default)


plotVar(nutri.res, comp = c(1,3), cutoff = 0.5)

## Not run: 
## variable representation for objects of class 'pls' or 'spls'
# ----------------------------------------------------
X <- liver.toxicity$gene
Y <- liver.toxicity$clinic
toxicity.spls <- spls(X, Y, ncomp = 3, keepX = c(50, 50, 50),
keepY = c(10, 10, 10))

plotVar(toxicity.spls, cex = c(1,0.8))

# with a customized legend
plotVar(toxicity.spls, legend = c("block 1", "my block 2"),
legend.title="my legend")

## variable representation for objects of class 'splsda'
# ----------------------------------------------------
X <- liver.toxicity$gene
Y <- as.factor(liver.toxicity$treatment[, 4])

ncomp <- 2
keepX <- rep(20, ncomp)

splsda.liver <- splsda(X, Y, ncomp = ncomp, keepX = keepX)
plotVar(splsda.liver)

## variable representation for objects of class 'sgcca' (or 'rgcca')
# ----------------------------------------------------
## see example in ??wrapper.sgcca
# need to unmap the Y factor diet
Y = unmap(nutrimouse$diet)
# set up the data as list
data = list(gene = nutrimouse$gene, lipid = nutrimouse$lipid, Y = Y)

# set up the design matrix:
# with this design, gene expression and lipids are connected to the diet factor
# design = matrix(c(0,0,1,
#                   0,0,1,
#                   1,1,0), ncol = 3, nrow = 3, byrow = TRUE)

# with this design, gene expression and lipids are connected to the diet factor
# and gene expression and lipids are also connected
design = matrix(c(0,1,1,
1,0,1,
1,1,0), ncol = 3, nrow = 3, byrow = TRUE)


#note: the penalty parameters will need to be tuned
wrap.result.sgcca = wrapper.sgcca(X = data, design = design, penalty = c(.3,.3, 1),
ncomp = 2,
scheme = "centroid")
wrap.result.sgcca

#variables selected on component 1 for each block
selectVar(wrap.result.sgcca, comp = 1, block = c(1,2))$'gene'$name
selectVar(wrap.result.sgcca, comp = 1, block = c(1,2))$'lipid'$name

#variables selected on component 2 for each block
selectVar(wrap.result.sgcca, comp = 2, block = c(1,2))$'gene'$name
selectVar(wrap.result.sgcca, comp = 2, block = c(1,2))$'lipid'$name

plotVar(wrap.result.sgcca, comp = c(1,2), block = c(1,2), comp.select = c(1,1),
title = c('Variables selected on component 1 only'))


plotVar(wrap.result.sgcca, comp = c(1,2), block = c(1,2), comp.select = c(2,2),
title = c('Variables selected on component 2 only'))

# -> this one shows the variables selected on both components
plotVar(wrap.result.sgcca, comp = c(1,2), block = c(1,2),
title = c('Variables selected on components 1 and 2'))

## variable representation for objects of class 'rgcca'
# ----------------------------------------------------

# need to unmap Y for an unsupervised analysis, where Y is included as a data block in data
Y = unmap(nutrimouse$diet)

data = list(gene = nutrimouse$gene, lipid = nutrimouse$lipid, Y = Y)
# with this design, all blocks are connected
design = matrix(c(0,1,1,1,0,1,1,1,0), ncol = 3, nrow = 3,
byrow = TRUE, dimnames = list(names(data), names(data)))

nutrimouse.rgcca <- wrapper.rgcca(X = data,
design = design,
tau = "optimal",
ncomp = 2,
scheme = "centroid")

plotVar(nutrimouse.rgcca, comp = c(1,2), block = c(1,2), cex = c(1.5, 1.5))


plotVar(nutrimouse.rgcca, comp = c(1,2), block = c(1,2))


# set up the data as list
data = list(gene = nutrimouse$gene, lipid = nutrimouse$lipid, Y =Y)
# with this design, gene expression and lipids are connected to the diet factor
# design = matrix(c(0,0,1,
#                   0,0,1,
#                   1,1,0), ncol = 3, nrow = 3, byrow = TRUE)

# with this design, gene expression and lipids are connected to the diet factor
# and gene expression and lipids are also connected
design = matrix(c(0,1,1,
1,0,1,
1,1,0), ncol = 3, nrow = 3, byrow = TRUE)
#note: the tau parameter is the regularization parameter
wrap.result.rgcca = wrapper.rgcca(X = data, design = design, tau = c(1, 1, 0),
ncomp = 2,
scheme = "centroid")
#wrap.result.rgcca
plotVar(wrap.result.rgcca, comp = c(1,2), block = c(1,2))


## End(Not run)

ajabadi/mixOmics2 documentation built on Aug. 9, 2019, 1:08 a.m.