gng.classify {DIME} | R Documentation |
Classification Based on GNG Model
Description
Classifies observed data into differential and non-differential groups based on GNG model.
Usage
gng.classify(data, obj, obj.cutoff = 0.1, obj.sigma.diff.cutoff = NULL,
obj.mu.diff.cutoff = NULL)
Arguments
data |
an R list of vector of normalized intensities (counts). Each element can correspond to particular chromosome. User can construct their own list containing only the chromosome(s) they want to analyze. |
obj |
a list object returned by |
obj.cutoff |
optional local fdr cutoff for classifying data into differential and non-differential groups based on GNG model. |
obj.sigma.diff.cutoff |
optional cut-off for standard deviation of the normal component in the best model to be declared as representing differential. |
obj.mu.diff.cutoff |
optional cut-off for standard deviation of the normal component in the best model to be declared as representing differential. |
Value
A list object passed as input with additional element $class containing vector of classifications for all the observations in data. A classification of 1 denotes that the data is classified as differential with fdr < obj.cutoff.
mu.diff.cutoff |
normal component with mean > mu.diff.cutoff will be used to represent differential component. |
sigma.diff.cutoff |
normal component with standard deviation > sigma.diff.cutoff will be used to represent differential component. |
Author(s)
Cenny Taslim taslim.2@osu.edu, with contributions from Abbas Khalili khalili@stat.ubc.ca, Dustin Potter potterdp@gmail.com, and Shili Lin shili@stat.osu.edu
See Also
Examples
library(DIME);
# generate simulated datasets with underlying exponential-normal components
N1 <- 1500; N2 <- 500; K <- 4; rmu <- c(-2.25,1.50); rsigma <- c(1,1);
rpi <- c(.05,.45,.45,.05); rbeta <- c(12,10);
set.seed(1234);
chr1 <- c(-rgamma(ceiling(rpi[1]*N1),shape = 1,scale = rbeta[1]),
rnorm(ceiling(rpi[2]*N1),rmu[1],rsigma[1]),
rnorm(ceiling(rpi[3]*N1),rmu[2],rsigma[2]),
rgamma(ceiling(rpi[4]*N1),shape = 1,scale = rbeta[2]));
chr2 <- c(-rgamma(ceiling(rpi[1]*N2),shape = 1,scale = rbeta[1]),
rnorm(ceiling(rpi[2]*N2),rmu[1],rsigma[1]),
rnorm(ceiling(rpi[3]*N2),rmu[2],rsigma[2]),
rgamma(ceiling(rpi[4]*N2),shape = 1,scale = rbeta[2]));
chr3 <- c(-rgamma(ceiling(rpi[1]*N2),shape = 1,scale = rbeta[1]),
rnorm(ceiling(rpi[2]*N2),rmu[1],rsigma[1]),
rnorm(ceiling(rpi[3]*N2),rmu[2],rsigma[2]),
rgamma(ceiling(rpi[4]*N2),shape = 1,scale = rbeta[2]));
# analyzing only chromosome 1 and chromosome 3
data <- list(chr1,chr3);
# fit GNG model with 2 normal components
test <- gng.fit(data, K = 2);
# vector of classification. 1 represents differential, 0 denotes non-differential
gngClass <- test$class;