comparison seqtk_seq.xml @ 0:7f1d97518adc draft default tip

planemo upload for repository www.github.com
author kyu
date Wed, 11 Apr 2018 19:46:44 -0400
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-1:000000000000 0:7f1d97518adc
1 <tool id="seqtk_seq" name="Convert to FASTA (seqtk)" version="0.1.0">
2 <requirements>
3 <requirement type="package" version="1.2">seqtk</requirement>
4 </requirements>
5 <command detect_errors="exit_code"><![CDATA[
6 seqtk seq -a "$input1" > "$output1"
7 ]]></command>
8 <inputs>
9 <param type="data" name="input1" format="fastq" />
10 </inputs>
11 <outputs>
12 <data name="output1" format="fasta" />
13 </outputs>
14 <tests>
15 <test>
16 <param name="input1" value="2.fastq"/>
17 <output name="output1" file="2.fasta"/>
18 </test>
19 </tests>
20 <help><![CDATA[
21
22 Usage: seqtk seq [options] <in.fq>|<in.fa>
23
24 Options: -q INT mask bases with quality lower than INT [0]
25 -X INT mask bases with quality higher than INT [255]
26 -n CHAR masked bases converted to CHAR; 0 for lowercase [0]
27 -l INT number of residues per line; 0 for 2^32-1 [0]
28 -Q INT quality shift: ASCII-INT gives base quality [33]
29 -s INT random seed (effective with -f) [11]
30 -f FLOAT sample FLOAT fraction of sequences [1]
31 -M FILE mask regions in BED or name list FILE [null]
32 -L INT drop sequences with length shorter than INT [0]
33 -c mask complement region (effective with -M)
34 -r reverse complement
35 -A force FASTA output (discard quality)
36 -C drop comments at the header lines
37 -N drop sequences containing ambiguous bases
38 -1 output the 2n-1 reads only
39 -2 output the 2n reads only
40 -V shift quality by '(-Q) - 33'
41 -U convert all bases to uppercases
42 -S strip of white spaces in sequences
43
44
45 ]]></help>
46 <citations>
47 <citation type="bibtex">
48 @misc{githubseqtk,
49 author = {LastTODO, FirstTODO},
50 year = {TODO},
51 title = {seqtk},
52 publisher = {GitHub},
53 journal = {GitHub repository},
54 url = {https://github.com/lh3/seqtk},
55 }</citation>
56 </citations>
57 </tool>