make_bed1
Find methylation in nanopore reads
Overview
/usr/lib/python3/dist-packages/joblib/_multiprocessing_helpers.py:53: UserWarning: [Errno 13] Permission denied. joblib will operate in serial mode
- warnings.warn('%s.
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joblib will operate in serial mode' % (e,))
usage: make_bed.py [-h] [-d MIN_READ_DEPTH] [-t MOD_THRESHOLD] -f MCALLER_FILE
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[-p POSITIONS] [--control] [--gff] [--ref REF] [--plot] [--plotsummary] [--plotdir PLOTDIR] [--vo] [-v]
Produce bed file of methylated positions based on mCaller output
optional arguments:
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-h, --help -
show this help message and exit
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-d MIN_READ_DEPTH, --min_read_depth MIN_READ_DEPTH -
minimum coverage of position to determine methylation (default = 15)
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-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)
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-f MCALLER_FILE, --mCaller_file MCALLER_FILE -
the output file from mCaller to summarize
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-p POSITIONS, --positions POSITIONS -
~bed file of positions for which to calculate % of methylated reads (chromosome,start,end,strand); ignores other thresholds
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--control -
take unmethylated positions as a control for motif detection
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--gff -
output PacBio-style gff instead of bed ("identificationQv" score will be average probability of methylation)
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--ref REF -
use reference fasta to output longer contexts surrounding a base, from
-20to +20
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--plot -
plot currents deviations at the positions included (not recommended for many positions)
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--plotsummary -
plot currents deviations summarized across the positions included
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--plotdir PLOTDIR -
output directory for plots, default=mCaller_position_plots
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--vo -
verbose output including probabilities for each position
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-v, --version -
print version
Releases
Unchanged in 2 releases since Debian 12 (Bookworm).