Description Usage Arguments Details Value Examples
Manhattan plot function for results of multiHiCcompare
1 2 3 4 5 6 7 | manhattan_hicexp(
hicexp,
method = "standard",
return_df = FALSE,
alpha = 0.05,
plot.chr = NA
)
|
hicexp |
A hicexp object that has had differences detected |
method |
string denoting the p-value method to use for plotting. Options are "standard", "fisher", "stouffer", "addCLT", and "count". "standard" plots a manhattan plot using all individual p-values (very slow, use with caution). "fisher" or "stouffer" methods use the Fisher's method or the Stouffer-Liptak method, respectively, for combining p-values for each region which are then plotted on the -log10(p-value) Y-axis. "addCLT" combines p-values using the BLMA package's addCLT function. "count" summarizes the number of times a region was detected as significant (see "alpha" parameter), plotted on Y-axis. The higher the dots are, the more sighificant/more frequent a region was detected as significantly differentially interacting. |
return_df |
Logical, should the data.frame used to generate the plot be returned? |
alpha |
The adjusted p-value cutoff to be used for calling an interaction significant. This is only used if method = 'count'. Defaults to 0.05. |
plot.chr |
A numeric value indicating a specific chromosome number to subset the plot to. Defaults to NA indicating that all chromosomes will be plotted. |
This function is used to create a manhattan
plot for the significance of all genomic regions
in the dataset. These correspond to the rows (or columns)
of the upper triangle of the full Hi-C matrix. Each genomic
region of the Hi-C dataset has multiple interactions it
is involved in and the significance of all of these can
be visualized with method = "standard"
.
Alternatively the p-values for all these interactions
can be combined using either Fisher's method or the
Stouffer-Liptak method of combining p-values. Additionally
the "count" option will plot based on the number of times
each region was found to be involved in a signficantly
different interaction. The
manhattan plot can be used to identify "hotspot"
regions of the genome where major differences
seem to be located based on the results of a multiHiCcompare
analysis.
A manhattan plot and optionally the data.frame used to generate the manhattan plot.
1 2 | data("hicexp_diff")
manhattan_hicexp(hicexp_diff, method = "fisher")
|
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