tcgsaseq (version 2.0.5)

vc_test_perm: Permutation-based variance component test statistic

Description

This function computes an approximation of the Variance Component test for a mixture of \(\chi^{2}\)s using permutations. This is preferable to the asymptotic approximation for small sample sizes. We rely on exact p-values following Phipson and Smyth, 2010 (see References).

Usage

vc_test_perm(
  y,
  x,
  indiv = rep(1, nrow(x)),
  phi,
  w,
  Sigma_xi = diag(ncol(phi)),
  n_perm = 1000,
  progressbar = TRUE,
  parallel_comp = TRUE,
  nb_cores = parallel::detectCores() - 1,
  genewise_pvals = FALSE,
  homogen_traj = FALSE,
  na.rm = FALSE
)

Arguments

y

a numeric matrix of dim G x n containing the raw RNA-seq counts for G genes from n samples.

x

a numeric design matrix of dim n x p containing the p covariates to be adjusted for

indiv

a vector of length n containing the information for attributing each sample to one of the studied individuals. Coerced to be a factor.

phi

a numeric design matrix of size n x K containing the K variables to be tested

w

a vector of length n containing the weights for the n samples.

Sigma_xi

a matrix of size K x K containing the covariance matrix of the K random effects.

n_perm

the number of perturbations. Default is 1000.

progressbar

logical indicating whether a progress bar should be displayed when computing permutations (only in interactive mode).

parallel_comp

a logical flag indicating whether parallel computation should be enabled. Only Linux and MacOS are supported, this is ignored on Windows. Default is TRUE.

nb_cores

an integer indicating the number of cores to be used when parallel_comp is TRUE. Only Linux and MacOS are supported, this is ignored on Windows. Default is parallel::detectCores() - 1.

genewise_pvals

a logical flag indicating whether gene-wise p-values should be returned. Default is FALSE in which case gene-set p-value is computed and returned instead.

homogen_traj

a logical flag indicating whether trajectories should be considered homogeneous. Default is FALSE in which case trajectories are not only tested for trend, but also for heterogeneity.

na.rm

logical: should missing values (including NA and NaN) be omitted from the calculations? Default is FALSE.

Value

A list with the following elements when the set p-value is computed :

• set_score_obs: the approximation of the observed set score

• set_pval: the associated set p-value

or a list with the following elements when gene-wise p-values are computed:

• gene_scores_obs: vector of approximating the observed gene-wise scores

• gene_pvals: vector of associated gene-wise p-values

• ds_fdr: vector of associated gene-wise discrete false discovery rates

References

Phipson B, and Smyth GK (2010). Permutation p-values should never be zero: calculating exact p-values when permutations are randomly drawn. Statistical Applications in Genetics and Molecular Biology, Volume 9, Issue 1, Article 39. http://www.statsci.org/smyth/pubs/PermPValuesPreprint.pdf

See Also

davies

Examples

# NOT RUN {
#rm(list=ls())
set.seed(123)

##generate some fake data
########################
n <- 100
r <- 12
t <- matrix(rep(1:3), 4, ncol=1, nrow=r)
sigma <- 0.4
b0 <- 1

#under the null:
b1 <- 0
#under the alternative:
b1 <- 0.5
y.tilde <- b0 + b1*t + rnorm(r, sd = sigma)
y <- t(matrix(rnorm(n*r, sd = sqrt(sigma*abs(y.tilde))), ncol=n, nrow=r) +
      matrix(rep(y.tilde, n), ncol=n, nrow=r))
x <- matrix(1, ncol=1, nrow=r)

#run test
permTestRes <- vc_test_perm(y, x, phi=t, w=matrix(1, ncol=ncol(y), nrow=nrow(y)),
                           indiv=rep(1:4, each=3), n_perm=50, #1000,
                           parallel_comp = FALSE)
permTestRes$set_pval

# }