comparison chira_collapse.xml @ 0:872249f5495a draft

"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/chira commit e4f841daf49048d6c656d50cffb344b53eebeec2"
author iuc
date Sun, 19 Jan 2020 16:32:04 -0500
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children 00187b27f5e5
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-1:000000000000 0:872249f5495a
1 <tool id="chira_collapse" name="ChiRA collapse" version="@WRAPPER_VERSION@0">
2 <description>deduplicate fastq reads</description>
3 <macros>
4 <import>macros.xml</import>
5 </macros>
6 <expand macro="requirements" />
7 <command><![CDATA[
8 chira_collapse.py
9 -i '$in'
10 -u '$umi_len'
11 -o '$out'
12 ]]></command>
13
14 <inputs>
15 <param format="fastq" name="in" type="data" label="Input FASTQ file"/>
16 <param name="umi_len" type="integer" value="0"
17 label="Length of the UMI if present at the 5' end of your reads"/>
18 </inputs>
19 <outputs>
20 <data format="fasta" name="out" label="ChiRA collapse FASTQ on ${on_string}"/>
21 </outputs>
22
23 <tests>
24 <test expect_num_outputs="1">
25 <param name="in" value="reads.fastq" />
26 <output name="out" file="reads.fasta" />
27 </test>
28 </tests>
29
30 <help>
31
32 .. class:: infomark
33
34 **What it does**
35
36 This tool deduplicates the reads from the FASTQ file and writes into a fasta each read once with it's read count.
37
38 **Inputs**
39
40 * Quality and adapter trimmed FASTQ file
41
42 **Outputs**
43
44 * FASTA file with unique sequences. The headers of the sequence are in the following format: >sequence_id|UMI|read_count
45
46 </help>
47 <expand macro="citations" />
48 </tool>