lociRead | R Documentation |
Module for reading interpreting loci argument. Used by various CC functions, including CCMap (implemented), CCBin and CCPileup
lociRead(loci = loci, features = features, chrom. = chrom., pos = pos)
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. |
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. |
Will Gittens
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