comparison sam_to_fastq.xml @ 0:4c60ceadc414 draft

planemo upload for repository https://github.com/ARTbio/tools-artbio/tree/master/tools/sam_to_fastq commit 8a467239b4e3aa42c448f5a088c399e53d50c3fd-dirty
author drosofff
date Mon, 21 Mar 2016 14:40:06 -0400
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-1:000000000000 0:4c60ceadc414
1 <tool id="sam_to_fastq" name="SAM to FASTQ" version="0.1">
2 <description></description>
3 <command interpreter="python">sam_to_fastq.py --input $input --output $output</command>
4 <inputs>
5 <param name="input" type="data" format="sam" label="SAM file for extraction of aligned reads in FASTQ format"/>
6 </inputs>
7
8 <outputs>
9 <data format="fastqsanger" name="output" label="FASTQ extraction" />
10 </outputs>
11
12 <tests>
13 <test>
14 <param ftype="fasta" name="input" value="input.sam" />
15 <output file="output.fastq" name="output" />
16 </test>
17 </tests>
18
19
20 <help>
21
22 **What it does**
23
24 Extract sequence and sequence quality of aligned reads in a SAM alignment file and return a FASTQ file containing those reads
25
26 </help>
27
28 </tool>