Provided by: filtlong_0.2.1-1_amd64
NAME
filtlong - quality filtering tool for Nanopore and PacBio reads
SYNOPSIS
filtlong {OPTIONS} [input_reads]
OPTIONS
positional arguments: input_reads input long reads to be filtered optional arguments: output thresholds: -t[int], --target_bases [int] keep only the best reads up to this many total bases -p[float], --keep_percent [float] keep only this percentage of the best reads (measured by bases) --min_length [int] minimum length threshold --min_mean_q [float] minimum mean quality threshold --min_window_q [float] minimum window quality threshold external references (if provided, read quality will be determined using these instead of from the Phred scores): -a[file], --assembly [file] reference assembly in FASTA format -1[file], --illumina_1 [file] reference Illumina reads in FASTQ format -2[file], --illumina_2 [file] reference Illumina reads in FASTQ format score weights (control the relative contribution of each score to the final read score): --length_weight [float] weight given to the length score (default: 1) --mean_q_weight [float] weight given to the mean quality score (default: 1) --window_q_weight [float] weight given to the window quality score (default: 1) read manipulation: --trim trim non-k-mer-matching bases from start/end of reads --split [split] split reads at this many (or more) consecutive non-k-mer-matching bases other: --window_size [int] size of sliding window used when measuring window quality (default: 250) --verbose verbose output to stderr with info for each read --version display the program version and quit -h, --help display this help menu For more information, go to: https://github.com/rrwick/Filtlong
AUTHOR
This manpage was written by Andreas Tille for the Debian distribution and can be used for any other usage of the program.