Description Usage Arguments Details Value Author(s) Examples
This function outputs the selected variables on each component for the sparse versions of the approaches (was also generalised to the non sparse versions for our internal functions).
1 |
object |
object of class inherited from |
comp |
integer value indicating the component of interest. |
block |
for an object of class |
list() |
other arguments. |
selectVar
provides the variables selected on a given component. \
outputs the name of the selected variables (provided that the input data have colnames) ranked in decreasing order of importance.
outputs the loading value for each selected variable, the loadings are ranked according to their absolute value.
These functions are only implemented for the sparse versions.
none
Kim-Anh LĂȘ Cao, Florian Rohart.
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 61 62 63 | X = liver.toxicity$gene
Y = liver.toxicity$clinic
# example with sPCA
# ------------------
liver.spca <- spca(X, ncomp = 1, keepX = 10)
selectVar(liver.spca, comp = 1)$name
selectVar(liver.spca, comp = 1)$value
## Not run:
#example with sIPCA
# -----------------
liver.sipca <- sipca(X, ncomp = 3, keepX = rep(10, 3))
selectVar(liver.sipca, comp = 1)
# example with sPLS
# -----------------
liver.spls = spls(X, Y, ncomp = 2, keepX = c(20, 40),keepY = c(5, 5))
selectVar(liver.spls, comp = 2)
# example with sPLS-DA
X = srbct$gene
Y = srbct$class
srbct.splsda = splsda(X, Y, ncomp = 2, keepX = c(5, 10))
select = selectVar(srbct.splsda, comp = 2)
select
# this is a very specific case where a data set has no rownames.
srbct$gene.name[substr(select$select, 2,5),]
# example with sGCCA
# -----------------
# ! need to unmap the Y factor
Y = unmap(nutrimouse$diet)
data = list(gene = nutrimouse$gene, lipid = nutrimouse$lipid,Y)
# in this design, gene expression and lipids are connected to the diet factor
# and gene expression and lipids are also connected
design = matrix(c(0,1,1,
1,0,1,
1,1,0), ncol = 3, nrow = 3, byrow = TRUE)
#note: the penalty parameters need to be tuned
wrap.result.sgcca = wrapper.sgcca(X = data, design = design, penalty = c(.3,.3, 1),
ncomp = 2,
scheme = "horst")
#variables selected and loadings values on component 1 for the two blocs
selectVar(wrap.result.sgcca, comp = 1, block = c(1,2))
#variables selected on component 1 for each block
selectVar(wrap.result.sgcca, comp = 1, block = c(1,2))$'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'$name
# loading value of the variables selected on the first block
selectVar(wrap.result.sgcca, comp = 1, block = 1)$'gene'$value
## End(Not run)
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