consensusSeekeR (version 1.0.2)

PING_nucleosome_positions: Nucleosome positions detected by the PING software using syntetic reads generated using a normal distribution. For demonstration purpose.

Description

Nucleosome positions detected by the PING software using syntetic reads generated using a normal distribution with a variance of 20 for regions chr1:10000-15000.

Usage

data(PING_nucleosome_positions)

Format

A GRanges containing one entry per detected nucleosome. The surronding ranges associated to those nucleosomes are in the dataset PING_nucleosome_positions.

References

• Sangsoon W, Zhang X, Sauteraud R, Robert F and Gottardo R. 2013. PING 2.0: An R/Bioconductor package for nucleosome positioning using next-generation sequencing data. Bioinformatics 29 (16): 2049-50.

See Also

• PING_nucleosome_ranges the associate genomic ranges dataset.
• findConsensusPeakRegions for extracting regions sharing nucleosomes from more than one experiment.

Examples

## Loading datasets
data(PING_nucleosome_positions)
data(PING_nucleosome_ranges)
data(NOrMAL_nucleosome_positions)
data(NOrMAL_nucleosome_ranges)
data(NucPosSimulator_nucleosome_positions)
data(NucPosSimulator_nucleosome_ranges)

## Assigning experiment name to each row of the dataset.
## Position and range datasets from the same sofware must
## have identical names.
names(PING_nucleosome_positions) <- rep("PING",
                            length(PING_nucleosome_positions))
names(PING_nucleosome_ranges) <- rep("PING",
                            length(PING_nucleosome_ranges))
names(NOrMAL_nucleosome_positions) <-rep("NOrMAL",
                            length(NOrMAL_nucleosome_positions))
names(NOrMAL_nucleosome_ranges) <- rep("NOrMAL",
                            length(NOrMAL_nucleosome_ranges))
names(NucPosSimulator_nucleosome_positions) <-rep("NucPosSimulator",
                            length(NucPosSimulator_nucleosome_positions))
names(NucPosSimulator_nucleosome_ranges) <- rep("NucPosSimulator",
                            length(NucPosSimulator_nucleosome_ranges))

## Calculating consensus regions for chromosome 1
## with a default region size of 20 bp (2 * extendingSize).
## The consensus regions are not resized to fit genomic ranges of the
## included nucleosomes.
## Nucleosomes from at least 2 software must be present in a region to
## be retained as a consensus region.
chrList <- Seqinfo(c("chr1"), c(249250621), NA)
findConsensusPeakRegions(
    narrowPeaks = c(PING_nucleosome_ranges,
                            NOrMAL_nucleosome_ranges,
                            NucPosSimulator_nucleosome_ranges),
    peaks = c(PING_nucleosome_positions,
                            NOrMAL_nucleosome_positions,
                            NucPosSimulator_nucleosome_positions),
    chrInfo = chrList,
    extendingSize = 10,
    expandToFitPeakRegion = FALSE,
    shrinkToFitPeakRegion = FALSE,
    minNbrExp = 3,
    nbrThreads = 1)