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LMGene (version 2.28.0)

tranest: Glog transformation parameter estimation function

Description

Estimates parameters for the glog transformation, by maximum likelihood or by minimizing the stability score.

Usage

tranest(eS, ngenes = -1, starting = FALSE, lambda = 1000, alpha = 0, gradtol = 1e-3, lowessnorm = FALSE, method=1, mult=FALSE, model=NULL, SD = FALSE, rank = TRUE, model.based = TRUE, rep.arrays = NULL)

Arguments

eS
An ExpressionSet object
ngenes
Number of genes to be used in parameter estimation. Default is to use all genes unless there are more than 100,000, in which case a subset of 50,000 genes is selected at random.
starting
If TRUE, user-specified starting values for lambda and alpha are input to the optimization routine
lambda
Starting value for parameter lambda. Ignored unless starting = TRUE
alpha
Starting value for parameter alpha. Ignored unless starting = TRUE
gradtol
A positive scalar giving the tolerance at which the scaled gradient is considered close enough to zero to terminate the algorithm
lowessnorm
If TRUE, lowess normalization (using lnorm) is used in calculating the likelihood.
method
Determines optimization method. Default is 1, which corresponds to a Newton-type method (see nlm and details.)
mult
If TRUE, tranest will use a vector alpha with one (possibly different) entry per sample. Default is to use same alpha for every sample. SD and mult may not both be TRUE.
model
Specifies model to be used. Default is to use all variables from eS without interactions. See details.
SD
If TRUE, transformation parameters are estimated by minimizing the stability score rather than by maximum likelihood. See details.
rank
If TRUE, the stability score is calculated by regressing the replicate standard deviations on the ranks of the gene/row means (rather than on the means themselves). Ignored unless SD = TRUE
model.based
If TRUE, the stability score is calculated using the standard deviations of residuals from the linear model in model. Ignored unless SD = TRUE
rep.arrays
List of sets of replicate arrays. Each element of rep.arrays should be a vector with entries corresponding to arrays (columns) in exprs(eS) conducted under the same experimental conditions, i.e., with identical rows in pData(eS). Ignored unless SD = TRUE and model.based = FALSE

Value

A list with components:
lambda
Estimate of transformation parameter lambda
alpha
Estimate of transformation parameter alpha

Details

If you have data in a matrix and information about experimental design factors, then you can use neweS to convert the data into an ExpressionSet object. Please see neweS for more detail.

The model argument is an optional character string, constructed like the right-hand side of a formula for lm. It specifies which of the variables in the ExpressionSet will be used in the model and whether interaction terms will be included. If model=NULL, it uses all variables from the ExpressionSet without interactions. Be careful of using interaction terms with factors; this often leads to overfitting, which will yield an error.

The default estimation method is maximum likelihood. The likelihood is derived by assuming that there exist values for lambda and alpha such that the residuals from the linear model in model, fit to glog-transformed data using those values for lambda and alpha, follow a normal distribution. See Durbin and Rocke (2003) for details.

If SD = TRUE, lambda and alpha are estimated by minimizing the stability score rather than by maximum likelihood. The stability score is defined as the absolute value of the slope coefficient from the regression of the replicate/residual standard deviation on the gene/row means, or on the rank of the gene/row means. If model.based = TRUE, the stability score is calculated using the standard deviation of residuals from the linear model in model. Otherwise, the stability score is calculated using the pooled standard deviation over sets of replicates in rep.arrays. See Wu and Rocke (2009) for details.

Optimization methods in method are as follows:

1 =
Newton-type method, using nlm

2 =
Nelder-Mead, using optim

3 =
BFGS, using optim

4 =
Conjugate gradients, using optim

5 =
Simulated annealing, using optim (may only be used when mult = TRUE)

References

Durbin, B.P and Rocke, D.M. (2003) Estimation of Transformation Parameters for Microarray Data, Bioinformatics, 19, 1360--1367.

Wu, S. and Rocke, D.M. (2009) Analysis of Illumina BeadArray data using variance stabilizing transformations.

http://dmrocke.ucdavis.edu

See Also

tranestAffyProbeLevel, lnorm, glog

Examples

Run this code
library(Biobase)
library(LMGene)

#data
data(sample.eS)

tranpar <- tranest(sample.eS, 100)
tranpar
tranpar <- tranest(sample.eS, mult=TRUE)
tranpar

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