Description Usage Arguments Details Value Author(s)
View source: R/scChIPseqFromBam.R
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1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 | scChIPseqFromBam(
label,
path,
genome,
bamFile,
binSize,
baseSeqDepth,
nCells,
relSeqDepthPerCell,
noisePerCell,
chromosome = "chr19",
basebinSize = 250,
outputRanges = TRUE,
excludeRegions = FALSE,
shuffleChunks = 5000,
shuffleProp = 0
)
|
label |
a character with the data label |
path |
a character with the path where the simulated data will be saved |
genome |
a character specifying the target genome |
bamFile |
a character specifying the path of the target alignment file |
binSize |
integer with the size of the bin window |
baseSeqDepth |
integer with the baseline sequencing depth for all simulated cells |
nCells |
integer with the number of cells to simulate |
relSeqDepthPerCell |
vector of size |
noisePerCell |
vector of size |
chromosome |
vector of chromosomes to consider from the specified genome. Default is
|
basebinSize |
integer giving the base bin size to calculate the gold-standard set of peaks. It must be smaller than binSize. Default 250 |
outputRanges |
a logical indicating whether ( |
excludeRegions |
a logical indicating whether to exclude blacklisted and gap regions or not. Default if FALSE |
shuffleChunks |
either NULL or an integer specifying the width of the size of the chunks to shuffle. If an integer, it must be divisible by basebinSize |
shuffleProp |
either NULL or the proportion of the genome to be shuffled |
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Pedro L. Baldoni, pedrobaldoni@gmail.com
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