discretizeExpressionData: Three-value discretization of gene expression data.

In RemyNicolle/CoRegNet-dev: CoRegNet : reconstruction and integrated analysis of co-regulatory networks

Description

Pre-process step to transform log2 numerical expression data into a three value categorical : over-expression (+1), under-expression (-1) and no change (0).

Usage

discretizeExpressionData(numericalExpression, threshold = NULL,
refSamples = NULL, standardDeviationThreshold = 1)

discretizeExpressionData(numericalExpression, threshold = NULL,
refSamples = NULL, standardDeviationThreshold = 1)

Arguments

numericalExpression	A matrix of continuous log2 gene expression data with genes in rows and samples in column.
threshold	A numeric value used as a fixed fold change threshold for brut discretization. Can be NULL if a standardDeviationThreshold is not.
refSamples	A vector of column names used as a set of reference samples to be used to compute fold changes. Can be NULL if the input data is already centered on a reference values (tested by the presence of negative values) or if the mean if each gene should be used to center (not scale) each expression values.
standardDeviationThreshold	The multplicator of the whole data set standard deviation to be used as the threshold.

Details

Given a continuous log2 gene epression matrix this function aims at producing a matrix of discretized expression values. The numerical data must be in some form of fold change to compare each value of a gene in a sample with a reference value of the same gene. The behavior of the function will therefore depend on the form of the input data.

Given a matrix with negative values, the function will consider that the data is already in the right format and will simply apply a hard threshold to discetize the data.

Given a matrix with only positive values, which is the case for normalized RNAseq or single color microarrays, the function will center each gene based on it's mean expression in all samples or based on the mean of expression of a set of reference sample (normal samples in a study of a particular disease for example).

In either case, the threshold will be used to transform the data in +1s if the value of a gene in a sample is above or equal to the threshold, -1s if the value is below the the negative value of the threshold and 0 otherwise.

The default is to compute a threshold based on the overall distribution of the numerical values in the dataset. This was choosen over a default fold change example (usually 1 or 2 corresponding to a two-fold or four-fold increase/decrease) after observing a large difference between technologies. However, the choice between a simple hard fold change threshold or a threshold as a multiplicator of the global standard deviation remains.

Value

A matrix of integers with the same number of rows and the same number of column as the input numericalExpression. Values in the output matrix are in -1,0,1. The reference samples are removed if given.

Author(s)

Remy Nicolle <remy.c.nicolle AT gmail.com>

Examples

# Use mean of each gene as a reference
expression=matrix(2*rnorm(200),nrow=2,dimnames=list(paste("gene",1:2,sep=""),paste("sample",1:100,sep="")))
discExp=discretizeExpressionData(expression)
boxplot(expression~discExp,xlab="Discrete values",ylab="Continuous values")
pie(table(discExp))
discExp=discretizeExpressionData(expression,standardDeviationThreshold=2)
pie(table(discExp))
discExp=discretizeExpressionData(expression,threshold=1)
pie(table(discExp))

# Use of reference sample
expression=matrix(2*rnorm(200),nrow=2,dimnames=list(paste("gene",1:2,sep=""),paste("sample",1:100,sep="")))
discExp=discretizeExpressionData(expression,refSamples=1:10)
boxplot(expression~discExp,xlab="Discrete values",ylab="Continuous values")
pie(table(discExp))
discExp=discretizeExpressionData(expression,standardDeviationThreshold=2,refSamples=1:10)
pie(table(discExp))
discExp=discretizeExpressionData(expression,threshold=1,refSamples=paste("sample",1:10,sep=""))
pie(table(discExp))

RemyNicolle/CoRegNet-dev documentation built on May 9, 2019, 9:40 a.m.