half.range.mode: Mode estimation for continuous data

In Bioconductor/genefilter: genefilter: methods for filtering genes from high-throughput experiments

Mode estimation for continuous data

Description

For data assumed to be drawn from a unimodal, continuous distribution, the mode is estimated by the “half-range” method. Bootstrap resampling for variance reduction may optionally be used.

Usage

half.range.mode(data, B, B.sample, beta = 0.5, diag = FALSE)

Arguments

data	A numeric vector of data from which to estimate the mode.
B	Optionally, the number of bootstrap resampling rounds to use. Note that B = 1 resamples 1 time, whereas omitting B uses data as is, without resampling.
B.sample	If bootstrap resampling is requested, the size of the bootstrap samples drawn from data. Default is to use a sample which is the same size as data. For large data sets, this may be slow and unnecessary.
beta	The fraction of the remaining range to use at each iteration.
diag	Print extensive diagnostics. For internal testing only... best left FALSE.

Details

Briefly, the mode estimator is computed by iteratively identifying densest half ranges. (Other fractions of the current range can be requested by setting beta to something other than 0.5.) A densest half range is an interval whose width equals half the current range, and which contains the maximal number of observations. The subset of observations falling in the selected densest half range is then used to compute a new range, and the procedure is iterated. See the references for details.

If bootstrapping is requested, B half-range mode estimates are computed for B bootstrap samples, and their average is returned as the final estimate.

Value

The mode estimate.

Author(s)

Richard Bourgon <[e-mail]>

References

• DR Bickel, “Robust estimators of the mode and skewness of continuous data.” Computational Statistics & Data Analysis 39:153-163 (2002).

• SB Hedges and P Shah, “Comparison of mode estimation methods and application in molecular clock analysis.” BMC Bioinformatics 4:31-41 (2003).

See Also

shorth

Examples

## A single normal-mixture data set

x <- c( rnorm(10000), rnorm(2000, mean = 3) )
M <- half.range.mode( x )
M.bs <- half.range.mode( x, B = 100 )

if(interactive()){
hist( x, breaks = 40 )
abline( v = c( M, M.bs ), col = "red", lty = 1:2 )
legend(
       1.5, par("usr")[4],
       c( "Half-range mode", "With bootstrapping (B = 100)" ),
       lwd = 1, lty = 1:2, cex = .8, col = "red"
       )
}

# Sampling distribution, with and without bootstrapping

X <- rbind(
           matrix( rnorm(1000 * 100), ncol = 100 ),
           matrix( rnorm(200 * 100, mean = 3), ncol = 100 )
           )
M.list <- list(
               Simple = apply( X, 2, half.range.mode ),
               BS = apply( X, 2, half.range.mode, B = 100 )
               )

if(interactive()){
boxplot( M.list, main = "Effect of bootstrapping" )
abline( h = 0, col = "red" )
}

Bioconductor/genefilter documentation built on Nov. 2, 2024, 7:24 a.m.