DOKK / manpages / debian 12 / mcaller / make_bed.1.en
MAKE_BED.PY(1) User Commands MAKE_BED.PY(1)

make_bed.py - find methylation in nanopore reads

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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

show this help message and exit
minimum coverage of position to determine methylation (default = 15)
minimum fraction of observations with probability of methylation >=50% at a position to include in report (default = 0.5)
the output file from mCaller to summarize
~bed file of positions for which to calculate % of methylated reads (chromosome,start,end,strand); ignores other thresholds
take unmethylated positions as a control for motif detection
output PacBio-style gff instead of bed ("identificationQv" score will be average probability of methylation)
use reference fasta to output longer contexts surrounding a base, from -20 to +20
plot currents deviations at the positions included (not recommended for many positions)
plot currents deviations summarized across the positions included
output directory for plots, default=mCaller_position_plots
verbose output including probabilities for each position
print version
June 2021 make_bed.py 1.0.3+git20210331.f7a616a