CCBin | R Documentation |
Bins yeast or human CC-seq data quickly using data.table. The outpout can be strand separated, or totalled, and can be in sparse or full format.
CCBin(
in.mode = "fullmap",
path.name = getwd(),
exp.name,
genome = "Cer3H4L2",
bin.width = 100,
os = 0,
mcal = F,
rDNAcal = F,
cal.path,
out.mode1 = "full",
out.mode2 = "strand",
plot.mode = "png",
violin = T,
ylims = "auto",
ARS.track = T,
cen.track = T,
names,
plotdimensions = "wide",
bg = "white",
samples,
lin.mod = F
)
in.mode |
Reading in .RDS file or a folder of FullMaps? Choose "rds" or "fullmap". Defaults to "rds". |
path.name |
A character string defining the RDS file or folder containing FullMaps. |
exp.name |
Manually specify a name for the experiment. |
genome |
Which genome has the data been aligned to? "Cer3H4L2", "W303" or "hg19". Defaults to "Cer3H4L2". |
bin.width |
What size bins, in bp? Defaults to 100. |
os |
Do you want to offset the Crick strand relative to the Watson strand prior to binning? Choose 3 for Top2, or 1 for Spo11. Choose 0 for no ofsetting. Defaults to 3. |
mcal |
normalise based of the mitochondria |
rDNAcal |
normalise based of the rDNA |
out.mode1 |
"sparse" or "full" format. Defaults to "full". Defaults to "full" |
out.mode2 |
Do you want to sum the Watson and Crick strands ("total") or report them seperately ("strand")? Defaults to "strand". |
plot.mode |
Do you want to plot the binned chromosome maps as "pdf" of "png"? Choose "none" for no plots |
ylims |
A single number specifying the maximum limit of the y axis, for both Watson and Crick. OR "auto", to automatically define for the entire set. |
bg |
Choose the background for the plots. Can be "none" (transparent), or "white". |
gene.track |
Do you want to plot the gene track? This is pretty pointless on whole chromosome plots. Awaiting a more sensible implementation. Defaults to FALSE. |
Will Gittens
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