@@ -18,21 +18,24 @@ Alternatively, use conda to install
1818Reads on stdin and writes to stdout.
1919
2020``` text
21- FLAGS:
22- -h, --help Prints help information
23- -V, --version Prints version information
24-
25- OPTIONS:
26- --headcrop Trim N nucleotides from the start of a read [default: 0]
27- --maxlength Sets a maximum read length
28- -l, --minlength Sets a minimum read length [default: 1]
29- -q, --quality Sets a minimum Phred average quality score [default: 0]
30- --tailcrop Trim N nucleotides from the end of a read [default: 0]
31- --threads Number of parallel threads to use [default: 4]
32- --contam Fasta file with reference to check potential contaminants against [default None]
33- -i, --input Input filename [default: read from stdin]
34- --maxgc Sets a maximum GC content [default: 1.0]
35- --mingc Sets a minimum GC content [default: 0.0]
21+ Usage: chopper [OPTIONS]
22+
23+ Options:
24+ -q, --quality <MINQUAL> Sets a minimum Phred average quality score [default: 0]
25+ --maxqual <MAXQUAL> Sets a maximum Phred average quality score [default: 1000]
26+ -l, --minlength <MINLENGTH> Sets a minimum read length [default: 1]
27+ --maxlength <MAXLENGTH> Sets a maximum read length
28+ --headcrop <HEADCROP> Trim N nucleotides from the start of a read [default: 0]
29+ --tailcrop <TAILCROP> Trim N nucleotides from the end of a read [default: 0]
30+ -t, --threads <THREADS> Use N parallel threads [default: 4]
31+ -c, --contam <CONTAM> Filter contaminants against a fasta
32+ --inverse Output the opposite of the normal results
33+ -i, --input <INPUT> Input filename [default: read from stdin]
34+ --maxgc <MAXGC> Filter max GC content [default: 1]
35+ --mingc <MINGC> Filter min GC content [default: 0]
36+ --trim <TRIM> Set a q-score cutoff to trim read ends
37+ -h, --help Print help
38+ -V, --version Print version
3639```
3740
3841EXAMPLES:
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