comparison sampleFasta.xml @ 3:e320ef2d105a draft

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author petr-novak
date Thu, 05 Sep 2019 09:04:56 -0400
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2:ff658cf87f16 3:e320ef2d105a
1 <tool id="sampler" name="Sequence sampling" version="1.0.0">
2 <description> Tool for creating samples of sequences from larger dataset</description>
3 <requirements>
4 <requirement type="package">seqkit</requirement>
5 </requirements>
6 <stdio>
7 <exit_code range="1:" level="fatal" description="Error" />
8 </stdio>
9 <command>
10 #if str($paired)=="true"
11 ${__tool_directory__}/deinterlacer.py $input Afile Bfile
12 &amp;&amp;
13 seqkit sample -2 --number $number --rand-seed $seed -o Asample -w 0 Afile
14 &amp;&amp;
15 seqkit sample -2 --number $number --rand-seed $seed -o Bsample -w 0 Bfile
16 &amp;&amp;
17 ${__tool_directory__}/fasta_interlacer.py -a Asample -b Bsample -p $output -x tmpfile
18 #else
19 seqkit sample -2 --number $number --rand-seed $seed -o $output -w 0 $input
20 #end if
21 </command>
22
23 <inputs>
24 <param format="fasta" type="data" name="input" label="Choose your fasta file" />
25 <param name="number" type="integer" size="7" value="500000" min="1" label="number of sequences or sequence pairs"/>
26 <param name="seed" type="integer" size="10" value="10" min="0" label="random number generator seed " />
27 <param name="paired" type="boolean" truevalue="true" falsevalue="false" checked="False" label="All sequence reads are paired" help="check if you are using pair reads and and input sequences contain both read mates and left mates alternate with their right mates"/>
28
29
30 </inputs>
31
32
33 <outputs>
34 <data format="fasta" name="output" label="Random selection from dataset ${input.hid}, sample size ${number})" />
35 </outputs>
36
37 <help>
38 **What it does**
39
40 This tools is intended to create sample of sequences from by taking 'random' sample from larger data sets.
41 Using a same seed parameter make sampling reproducible.
42
43
44 </help>
45
46
47 </tool>