CCFold | R Documentation |
Bins, loess smooths and calculates folds of yeast or human CC-seq data quickly using data.table.
CCFold(
in.mode = "fullmap",
s.dir = getwd(),
c.dir,
exp.name,
genome = "Cer3H4L2",
bin.width = 100,
sc = 80,
si = 100,
os = 0,
mcal = F,
rDNAcal = F,
cal.path,
out.mode1 = "full",
out.mode2 = "strand",
plot.mode = T,
ylims = "auto",
gene.track = F,
ARS.track = T,
names
)
in.mode |
Reading in .RDS file or a folder of FullMaps? Choose "rds" or "fullmap". Defaults to "rds". |
s.dir |
A character string defining the RDS file or folder containing the SAMPLE FullMaps. |
c.dir |
A character string defining the RDS file or folder containing the CONTROL 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. |
sc |
Parameter which changes the "span" of the smooth. Higher numbers will give a broader smooth. |
si |
Parameter which alters the final number of points of the smooth curve to be plotted. Defaults to 100 bp. |
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. |
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? (T/F). Defaults to TRUE. |
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. |
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. |
names |
Can specify your own vector of alias names for the libraries. |
Will Gittens
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