gpatterns.global_meth_trend | R Documentation |
calculates the average methylation (m / m + um)
in each
bin of strat_track
and plots it. By default, plots the average methylation
in different bins of CpG content. This can be used as a sanity check for methylation
data - in general, methylation is high for regions with low CpG density,
and low for CpG dense regions (e.g. CpG islands).
gpatterns.global_meth_trend(
tracks,
strat_track = .gpatterns.cg_cont_500_track,
strat_breaks = seq(0, 0.08, by = 0.002),
intervals = .gpatterns.genome_cpgs_intervals,
iterator = .gpatterns.genome_cpgs_intervals,
min_cov = NULL,
min_cgs = NULL,
names = NULL,
groups = NULL,
group_name = NULL,
include.lowest = TRUE,
ncol = 2,
nrow = 2,
width = 600,
height = 560,
fig_fn = NULL,
xlab = strat_track,
ylim = c(0, 1),
title = "",
legend = TRUE,
colors = NULL,
parallel = getOption("gpatterns.parallel")
)
tracks |
tracks to plot |
strat_track |
track to stratify average methylation by. default is CG content |
strat_breaks |
breaks to determine the bins of strat_track |
intervals |
genomic scope for which the function is applied |
iterator |
track expression iterator (of both tracks and strat_track) |
min_cov |
minimal coverage of each track |
min_cgs |
minimal number of CpGs per bin |
names |
alternative names for the track |
groups |
a vector the same length of |
group_name |
name of the grouping variable (e.g. tumor, sample, patient, experiment) |
include.lowest |
if 'TRUE', the lowest value of the range determined by breaks is included |
ncol |
number of columns |
nrow |
number of rows |
width |
plot width (if fig_fn is not NULL) |
height |
plot height (if fig_fn is not NULL) |
fig_fn |
output filename for the figure (if NULL, figure would be returned) |
xlab |
label for the x axis |
ylim |
ylim of the plot |
title |
title for the plot |
legend |
add legend |
colors |
custom colors |
parallel |
get trends parallely |
list with trend data frame (under 'trend') and the plot (under 'p')
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