gextract_meth | R Documentation |
gextract methylation data
gextract_meth(
tracks,
names = NULL,
intervals = gintervals.all(),
iterator = "intervs.global.seq_CG",
d_expand = NULL,
join_intervals = FALSE,
extract_meth_calls = FALSE,
avg_tracks = NULL,
avg_tracks_names = NULL,
annot_tracks = NULL,
annot_tracks_names = NULL,
min_cov = NULL,
...
)
tracks |
name of methylation track suffix (without ".cov" or ".meth") |
names |
sets the columns names in the returned value. |
intervals |
genomic scope for which the function is applied |
iterator |
track expression iterator. If "NULL" iterator is based on CpGs |
d_expand |
smooth the methylation signal |
join_intervals |
add the intervals to the returned data frame (using left_join) |
extract_meth_calls |
extract also methylation calls (".meth" tracks) |
avg_tracks |
tracks of average methylation (for tracks that do not have ".cov" and ".meth" tracks) |
avg_tracks_names |
names of tracks in |
annot_tracks |
other tracks to extract |
annot_tracks_names |
names of annotation tracks |
min_cov |
minimal coverage per track. If the coverage is below this number the methylation values would be changed to NA. |
... |
additional arguments to gextract |
data frame with a column with average methylation for each track, and another column with ".cov" suffix with every track's coverage. If extract_meth_calls
is TRUE - additional columns with ".meth" suffix with number of methylation calls per track.
gextract
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