Provided by: nanofilt_2.6.0-4_all 

NAME
NanoFilt - filtering and trimming of long read sequencing data
DESCRIPTION
usage: NanoFilt [-h] [-v] [--logfile LOGFILE] [-l LENGTH]
[--maxlength MAXLENGTH] [-q QUALITY] [--minGC MINGC] [--maxGC MAXGC] [--headcrop HEADCROP]
[--tailcrop TAILCROP] [-s SUMMARY] [--readtype {1D,2D,1D2}] [input]
Perform quality and/or length and/or GC filtering of (long read) fastq data. Reads on stdin.
General options:
-h, --help
show the help and exit
-v, --version
Print version and exit.
--logfile LOGFILE
Specify the path and filename for the log file.
input input, uncompressed fastq file
Options for filtering reads on.:
-l LENGTH, --length LENGTH
Filter on a minimum read length
--maxlength MAXLENGTH
Filter on a maximum read length
-q QUALITY, --quality QUALITY
Filter on a minimum average read quality score
--minGC MINGC
Sequences must have GC content >= to this. Float between 0.0 and 1.0. Ignored if using summary
file.
--maxGC MAXGC
Sequences must have GC content <= to this. Float between 0.0 and 1.0. Ignored if using summary
file.
Options for trimming reads.:
--headcrop HEADCROP
Trim n nucleotides from start of read
--tailcrop TAILCROP
Trim n nucleotides from end of read
Input options.:
-s SUMMARY, --summary SUMMARY
Use albacore or guppy summary file for quality scores
--readtype {1D,2D,1D2}
Which read type to extract information about from summary. Options are 1D, 2D or 1D2
EXAMPLES:
gunzip -c reads.fastq.gz | NanoFilt -q 10 -l 500 --headcrop 50 | minimap2 genome.fa - | samtools
sort -O BAM -@24 -o alignment.bam - gunzip -c reads.fastq.gz | NanoFilt -q 12 --headcrop 75 | gzip
> trimmed-reads.fastq.gz gunzip -c reads.fastq.gz | NanoFilt -q 10 | gzip >
highQuality-reads.fastq.gz
SEE ALSO
The full documentation for NanoFilt is maintained as a Texinfo manual. If the info and NanoFilt programs
are properly installed at your site, the command
info NanoFilt
should give you access to the complete manual.
NanoFilt 2.6.0 June 2020 NANOFILT(1)