deepSNV-class {deepSNV} | R Documentation

## deepSNV class.

### Description

This class stores the contents of the deepSNV test. It is typically initialized with `deepSNV`. This class has the following slots:

p.val

  The P-values of the test.

test

  A matrix with the nucleotide counts in the test experiment. The column names of the nucleotide counts are A, T, C, G, - for the positivie strand and a, t, c, g, _ for the reverse.

control

  A matrix with the nucleotide counts in the control experiment. The column names must be the same as for the test.

coordinates

  A `data.frame` with the genomic coordinates chr and pos, and other columns, if desired.

dirichlet.prior

  A matrix with the nucleotide-specific Dirichlet prior

pseudo.count

  The pseudo count if used)

alternative

  A string with the alternative used in the test.

nucleotides

  A character vector with the nucleotides tested.

regions

  A `data.frame` with columns chr, start, and stop.

files

  A list with two entries test and control storing the filenames (if the object was initialized from two bam-files).

combine.method

  The method for combining p-values as a character string.

model

  The statistical model, either bin for binomial, or betabin for beta-binomial

over.dispersion

  If the model is beta-binomial, the first parameter for the beta-binomial model, which is shared across sites.

call

  The last function call to deepSNV.

log.lik

  The log likelihood of the data under the null hypothesis. (Excluding zeros on the opposite site under a one-sided test.)

### Author(s)

Moritz Gerstung

### See Also

`deepSNV`

### Examples

    ## Short example with 2 SNVs at frequency ~10%
    regions <- data.frame(chr="B.FR.83.HXB2_LAI_IIIB_BRU_K034", start = 3120, stop=3140)
    ex <- deepSNV(test = system.file("extdata", "test.bam", package="deepSNV"), control = system.file("extdata", "control.bam", package="deepSNV"), regions=regions, q=10)
    show(ex)   # show method
    plot(ex)   # scatter plot
    summary(ex)   # summary with significant SNVs
    ex[1:3,]   # subsetting the first three genomic positions
    tail(test(ex, total=TRUE))   # retrieve the test counts on both strands
    tail(control(ex, total=TRUE))

    ## Not run: Full example with ~ 100 SNVs. Requires an internet connection, but try yourself.
    # regions <- data.frame(chr="B.FR.83.HXB2_LAI_IIIB_BRU_K034", start = 2074, stop=3585)
    # HIVmix <- deepSNV(test = "http://www.bsse.ethz.ch/cbg/software/deepSNV/data/test.bam", control = "http://www.bsse.ethz.ch/cbg/software/deepSNV/data/control.bam", regions=regions, q=10)
    data(HIVmix) # attach data instead..
    show(HIVmix)
    plot(HIVmix)
    head(summary(HIVmix))

[Package deepSNV version 1.28.0 Index]