rise.screen: Perform the screening stage of RISE: Two-Stage Rank-Based...

View source: R/rise.screen.R

rise.screenR Documentation

Perform the screening stage of RISE: Two-Stage Rank-Based Identification of High-Dimensional Surrogate Markers

Description

A set of high-dimensional surrogate candidates are screened one-by-one to identify strong candidates. Strength of surrogacy is assessed through a rank-based measure of the similarity in treatment effects on a candidate surrogate and the primary response. P-values corresponding to hypothesis testing on this measure are corrected for the high number of statistical tests performed.

Usage

rise.screen(
  yone,
  yzero,
  sone,
  szero,
  alpha = 0.05,
  power.want.s = NULL,
  epsilon = NULL,
  u.y.hyp = NULL,
  p.correction = "BH",
  n.cores = 1,
  alternative = "less",
  paired = FALSE,
  return.all.screen = TRUE
)

Arguments

yone

numeric vector of primary response values in the treated group.

yzero

numeric vector of primary response values in the untreated group.

sone

matrix or dataframe of surrogate candidates in the treated group with dimension n1 x p where n1 is the number of treated samples and p the number of candidates. Sample ordering must match exactly yone.

szero

matrix or dataframe of surrogate candidates in the untreated group with dimension n0 x p where n0 is the number of untreated samples and p the number of candidates. Sample ordering must match exactly yzero.

alpha

significance level for determining surrogate candidates. Default is 0.05.

power.want.s

numeric in (0,1) - power desired for a test of treatment effect based on the surrogate candidate. Either this or epsilon argument must be specified.

epsilon

numeric in (0,1) - non-inferiority margin for determining surrogate validity. Either this or power.want.s argument must be specified.

u.y.hyp

hypothesised value of the treatment effect on the primary response on the probability scale. If not given, it will be estimated based on the observations.

p.correction

character. Method for p-value adjustment (see p.adjust() function). Defaults to the Benjamini-Hochberg method ("BH").

n.cores

numeric giving the number of cores to commit to parallel computation in order to improve computational time through the pbmcapply() function. Defaults to 1.

alternative

character giving the alternative hypothesis type. One of c("less","two.sided"), where "less" corresponds to a non-inferiority test and "two.sided" corresponds to a two one-sided test procedure. Default is "less".

paired

logical flag giving if the data is independent or paired. If FALSE (default), samples are assumed independent. If TRUE, samples are assumed to be from a paired design. The pairs are specified by matching the rows of yone and sone to the rows of yzero and szero.

return.all.screen

logical flag. If TRUE (default), a dataframe will be returned giving the screening results for all candidates. Else, only the significant candidates will be returned.

Value

a list with elements

  • screening.metrics : dataframe of screening results (for each candidate marker - delta, CI, sd, epsilon, p-values).

  • significant.markers: character vector of markers with p_adjusted < alpha

  • screening.weights: dataframe giving marker names and the inverse absolute value of the associated deltas.

Author(s)

Arthur Hughes

Examples

# Load high-dimensional example data
data("example.data.highdim")
yone <- example.data.highdim$y1
yzero <- example.data.highdim$y0
sone <- example.data.highdim$s1
szero <- example.data.highdim$s0

rise.screen.result <- rise.screen(yone, yzero, sone, szero, power.want.s = 0.8)


SurrogateRank documentation built on June 8, 2025, 10:27 a.m.