Provided by: scythe_0.994+git20141017.20d3cff-2_amd64
NAME
scythe - Bayesian adaptor trimmer
SYNOPSIS
scythe -t sanger -a /path/to/adaptors.fasta [options] <sequences.fastq.gz> Trim 3´-end adaptor contaminants off sequence files. If no output file is specified, scythe will use stdout.
OPTIONS
-p, --prior prior (default: 0.300) -q, --quality-type quality type, either illumina, solexa, or sanger (default: sanger) -m, --matches-file matches file (default: no output) -o, --output-file output trimmed sequences file (default: stdout) -t, --tag add a tag to the header indicating Scythe cut a sequence (default: off) -n, --min-match smallest contaminant to consider (default: 5) -M, --min-keep filter sequences less than or equal to this length (default: 35) --quiet don´t output statistics about trimming to stdout (default: off) --help display this help and exit --version output version information and exit These are the quality encoding schemes scythe recognises (see ´--quality´) phred PHRED quality scores (e.g. from Roche 454). ASCII with no offset, range: [4, 60]. sanger Sanger are PHRED ASCII qualities with an offset of 33, range: [0, 93]. From NCBI SRA, or Illumina pipeline 1.8+. solexa Solexa (also very early Illumina -- pipeline < 1.3). ASCII offset of 64, range: [-5, 62]. Uses a different quality-to-probabilities conversion than other schemes. illumina Illumina output from pipeline versions between 1.3 and 1.7. ASCII offset of 64, range: [0, 62]
FILES
adaptors.fasta: Provide contaminant sequences as a fasta-formatted file. See ´/usr/share/doc/scythe/illumina_adaptors.fa´. N.B.: Index/Barcode sequences should be substituted for Ns in the example adaptor file.
AUTHOR
Vince Buffalo, https://github.com/vsbuffalo