tune.block.splsda: Tuning function for block.splsda method (N-integration with...

In ajabadi/mixOmics2: Omics Data Integration Project

Description

Computes M-fold or Leave-One-Out Cross-Validation scores based on a user-input grid to determine the optimal parsity parameters values for method block.splsda.

Usage

tune.block.splsda(X, Y, indY, ncomp = 2, test.keepX, already.tested.X,
  validation = "Mfold", folds = 10, dist = "max.dist",
  measure = "BER", weighted = TRUE, progressBar = TRUE,
  tol = 1e-06, max.iter = 100, near.zero.var = FALSE, nrepeat = 1,
  design, scheme = "horst", scale = TRUE, init = "svd",
  light.output = TRUE, cpus, name.save = NULL)

Arguments

X	numeric matrix of predictors. NAs are allowed.
Y	if(method = 'spls') numeric vector or matrix of continuous responses (for multi-response models) NAs are allowed.
indY	To be supplied if Y is missing, indicates the position of the matrix / vector response in the list X
ncomp	the number of components to include in the model.
test.keepX	A list of length the number of blocks in X (without the outcome). Each entry of this list is a numeric vector for the different keepX values to test for that specific block.
already.tested.X	Optional, if ncomp > 1 A numeric vector indicating the number of variables to select from the X data set on the firsts components.
validation	character. What kind of (internal) validation to use, matching one of "Mfold" or "loo" (see below). Default is "Mfold".
folds	the folds in the Mfold cross-validation. See Details.
dist	distance metric to use for splsda to estimate the classification error rate, should be a subset of "centroids.dist", "mahalanobis.dist" or "max.dist" (see Details).
measure	Two misclassification measure are available: overall misclassification error overall or the Balanced Error Rate BER
weighted	tune using either the performance of the Majority vote or the Weighted vote.
progressBar	by default set to TRUE to output the progress bar of the computation.
tol	Convergence stopping value.
max.iter	integer, the maximum number of iterations.
near.zero.var	boolean, see the internal nearZeroVar function (should be set to TRUE in particular for data with many zero values). Default value is FALSE
nrepeat	Number of times the Cross-Validation process is repeated.
design	numeric matrix of size (number of blocks in X) x (number of blocks in X) with 0 or 1 values. A value of 1 (0) indicates a relationship (no relationship) between the blocks to be modelled. If Y is provided instead of indY, the design matrix is changed to include relationships to Y.
scheme	Either "horst", "factorial" or "centroid". Default = centroid, see reference.
scale	boleean. If scale = TRUE, each block is standardized to zero means and unit variances. Default = TRUE.
init	Mode of initialization use in the algorithm, either by Singular Value Decompostion of the product of each block of X with Y ("svd") or each block independently ("svd.single"). Default = svd.
light.output	if set to FALSE, the prediction/classification of each sample for each of test.keepX and each comp is returned.
cpus	Number of cpus to use when running the code in parallel.
name.save	character string for the name of the file to be saved.

Details

This tuning function should be used to tune the keepX parameters in the block.splsda function (N-integration with sparse Discriminant Analysis).

M-fold or LOO cross-validation is performed with stratified subsampling where all classes are represented in each fold.

If validation = "Mfold", M-fold cross-validation is performed. The number of folds to generate is to be specified in the argument folds.

If validation = "loo", leave-one-out cross-validation is performed. By default folds is set to the number of unique individuals.

All combination of test.keepX values are tested. A message informs how many will be fitted on each component for a given test.keepX.

More details about the prediction distances in ?predict and the supplemental material of the mixOmics article (Rohart et al. 2017). Details about the PLS modes are in ?pls.

BER is appropriate in case of an unbalanced number of samples per class as it calculates the average proportion of wrongly classified samples in each class, weighted by the number of samples in each class. BER is less biased towards majority classes during the performance assessment.

Value

A list that contains:

error.rate	returns the prediction error for each test.keepX on each component, averaged across all repeats and subsampling folds. Standard deviation is also output. All error rates are also available as a list.
choice.keepX	returns the number of variables selected (optimal keepX) on each component, for each block.
choice.ncomp	returns the optimal number of components for the model fitted with $choice.keepX.
error.rate.class	returns the error rate for each level of Y and for each component computed with the optimal keepX
predict	Prediction values for each sample, each test.keepX, each comp and each repeat. Only if light.output=FALSE
class	Predicted class for each sample, each test.keepX, each comp and each repeat. Only if light.output=FALSE
cor.value	compute the correlation between latent variables for two-factor sPLS-DA analysis.

Author(s)

Florian Rohart, Amrit Singh, Kim-Anh Lê Cao.

References

Method:

Singh A., Gautier B., Shannon C., Vacher M., Rohart F., Tebbutt S. and Lê Cao K.A. (2016). DIABLO: multi omics integration for biomarker discovery.

mixOmics article:

Rohart F, Gautier B, Singh A, Lê Cao K-A. mixOmics: an R package for 'omics feature selection and multiple data integration. PLoS Comput Biol 13(11): e1005752

See Also

block.splsda and http://www.mixOmics.org for more details.

Examples

# this is the X data as a list of mRNA and miRNA; the Y data set is a single data set of proteins
data = list(mrna = breast.TCGA$data.train$mrna, mirna = breast.TCGA$data.train$mirna,
protein = breast.TCGA$data.train$protein)
# set up a full design where every block is connected
# could also consider other weights, see our mixOmics manuscript
design = matrix(1, ncol = length(data), nrow = length(data),
dimnames = list(names(data), names(data)))
diag(design) =  0
design
# set number of component per data set
ncomp = 5

# Tuning the first two components
# -------------
## Not run: 
# definition of the keepX value to be tested for each block mRNA miRNA and protein
# names of test.keepX must match the names of 'data'
test.keepX = list(mrna = seq(10,40,20), mirna = seq(10,30,10), protein = seq(1,10,5))

# the following may take some time to run, note that for through tuning
# nrepeat should be > 1
tune = tune.block.splsda(X = data, Y = breast.TCGA$data.train$subtype,
ncomp = ncomp, test.keepX = test.keepX, design = design, nrepeat = 3)

tune$choice.ncomp
tune$choice.keepX



# Only tuning the second component
# -------------

already.mrna = 4 # 4 variables selected on comp1 for mrna
already.mirna  = 2 # 2 variables selected on comp1 for mirna
already.prot  = 1 # 1 variables selected on comp1 for protein

already.tested.X = list(mrna = already.mrna, mirna = already.mirna, prot = already.prot)

tune = tune.block.splsda(X = data, Y = breast.TCGA$data.train$subtype,
ncomp = 2, test.keepX = test.keepX, design = design,
already.tested.X = already.tested.X)

tune$choice.keepX

## End(Not run)

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