make_bed.py - find methylation in nanopore reads
/usr/lib/python3/dist-packages/joblib/_multiprocessing_helpers.py:53:
UserWarning: [Errno 13] Permission denied. joblib will operate in serial
mode
- warnings.warn('%s.
- joblib will operate in serial mode' % (e,))
usage: make_bed.py [-h] [-d MIN_READ_DEPTH] [-t MOD_THRESHOLD]
-f MCALLER_FILE
- [-p POSITIONS] [--control] [--gff] [--ref REF] [--plot] [--plotsummary]
[--plotdir PLOTDIR] [--vo] [-v]
Produce bed file of methylated positions based on mCaller
output
- -h, --help
- show this help message and exit
- -d MIN_READ_DEPTH,
--min_read_depth MIN_READ_DEPTH
- minimum coverage of position to determine methylation (default = 15)
- -t MOD_THRESHOLD,
--mod_threshold MOD_THRESHOLD
- minimum fraction of observations with probability of methylation >=50%
at a position to include in report (default = 0.5)
- -f MCALLER_FILE,
--mCaller_file MCALLER_FILE
- the output file from mCaller to summarize
- -p POSITIONS,
--positions POSITIONS
- ~bed file of positions for which to calculate % of methylated reads
(chromosome,start,end,strand); ignores other thresholds
- --control
- take unmethylated positions as a control for motif detection
- --gff
- output PacBio-style gff instead of bed ("identificationQv" score
will be average probability of methylation)
- --ref REF
- use reference fasta to output longer contexts surrounding a base, from
-20 to +20
- --plot
- plot currents deviations at the positions included (not recommended for
many positions)
- --plotsummary
- plot currents deviations summarized across the positions included
- --plotdir
PLOTDIR
- output directory for plots, default=mCaller_position_plots
- --vo
- verbose output including probabilities for each position
- -v, --version
- print version