Mercurial > repos > devteam > tabular_to_fastq
annotate tabular_to_fastq.xml @ 1:7bde4f066435 draft
planemo upload commit 33927a87ba2eee9bf0ecdd376a66241b17b3d734
author | devteam |
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date | Tue, 13 Oct 2015 12:45:21 -0400 |
parents | 9ae652b76979 |
children | 643018aa1435 |
rev | line source |
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0 | 1 <tool id="tabular_to_fastq" name="Tabular to FASTQ" version="1.0.0"> |
2 <description>converter</description> | |
3 <requirements> | |
4 <requirement type="package" version="1.0.0">galaxy_sequence_utils</requirement> | |
5 </requirements> | |
6 <command interpreter="python">tabular_to_fastq.py '$input_file' '$output_file' '$identifier' '$sequence' '$quality'</command> | |
7 <inputs> | |
8 <param name="input_file" type="data" format="tabular" label="Tabular file to convert" /> | |
9 <param name="identifier" label="Identifier column" type="data_column" data_ref="input_file" /> | |
10 <param name="sequence" label="Sequence column" type="data_column" data_ref="input_file" /> | |
11 <param name="quality" label="Quality column" type="data_column" data_ref="input_file" /> | |
12 </inputs> | |
13 <outputs> | |
14 <data name="output_file" format="fastq" /> | |
15 </outputs> | |
16 <tests> | |
17 <!-- basic test --> | |
18 <test> | |
19 <param name="input_file" value="fastq_to_tabular_out_1.tabular" ftype="tabular" /> | |
20 <param name="identifier" value="1" /> | |
21 <param name="sequence" value="2" /> | |
22 <param name="quality" value="3" /> | |
23 <output name="output_file" file="sanger_full_range_original_sanger.fastqsanger" /> | |
24 </test> | |
25 <!-- color space test --> | |
26 <test> | |
27 <param name="input_file" value="fastq_to_tabular_out_2.tabular" ftype="tabular" /> | |
28 <param name="identifier" value="1" /> | |
29 <param name="sequence" value="2" /> | |
30 <param name="quality" value="3" /> | |
31 <output name="output_file" file="sanger_full_range_as_cssanger.fastqcssanger" /> | |
32 </test> | |
33 </tests> | |
34 <help> | |
35 **What it does** | |
36 | |
37 This tool attempts to convert a tabular file containing sequencing read data to a FASTQ formatted file. The FASTQ Groomer tool should always be used on the output of this tool. | |
38 | |
39 </help> | |
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40 |
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41 <citations> |
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42 <citation type="doi">10.1093/bioinformatics/btq281</citation> |
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43 </citations> |
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44 |
0 | 45 </tool> |