Provided by: nanofilt_2.8.0-1_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)