View source: R/fit.interaction.model.R
fit.interaction.model | R Documentation |
Using a meta-analysis dataset take two features and Cox model them separately and together and extract HRs and p-values.
fit.interaction.model( feature1, feature2, expression.data, survival.data, data.type.ordinal = FALSE, centre.data = "median" )
feature1 |
String indicate what feature (gene/probe/etc.) should be extracted for analysis |
feature2 |
String indicate what feature (gene/probe/etc.) should be extracted for analysis |
expression.data |
A list where each component is an expression matrix (patients = columns, features = rows) for a different dataset |
survival.data |
A list where each component is an object of class Surv |
data.type.ordinal |
Logical indicating whether to treat this datatype as ordinal. Defaults to FALSE |
centre.data |
A character string specifying the centre value to be used for scaling data. Valid values are: 'median', 'mean', or a user defined numeric threshold e.g. '0.3' when modelling methylation beta values. This value is used for both scaling as well as for dichotomising data for estimating univariate betas from Cox model. Defaults to 'median' |
The interaction model compares cases where feature1 and feature2 concord (both high or both low) to those where they do not. That is, the model is y = x1 + x2 + (x1 == x2) and not the typical y = x1 + x2 + x1:x2
Returns a vector of six elements containing (HR,P) pairs for feature1, feature2, and the interaction
Syed Haider & Paul C. Boutros
data.dir <- get.program.defaults()[["test.data.dir"]]; data.types <- c("mRNA"); x1 <- load.cancer.datasets( datasets.to.load = c('Breastdata1'), data.types = data.types, data.directory = data.dir ); x2 <- fit.interaction.model( feature1 = "1000_at", feature2 = "2549_at", expression.data = x1$all.data[[data.types[1]]], survival.data = x1$all.survobj );
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