comparison merge_pcr_duplicates.xml @ 2:de4ea3aa1090 draft

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author rnateam
date Thu, 22 Oct 2015 10:26:45 -0400
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1:ae0f58d3318f 2:de4ea3aa1090
1 <tool id="merge_pcr_duplicates.py" name="merge_pcr_duplicates.py" version="1.0">
2 <description>Merge PCR duplicates according to random barcode library.</description>
3 <macros>
4 <import>macros.xml</import>
5 </macros>
6 <expand macro="requirements" />
7 <expand macro="stdio" />
8 <version_command>python merge_pcr_duplicates.py --version</version_command>
9 <command interpreter="python"><![CDATA[merge_pcr_duplicates.py
10 #if $positional_1 and $positional_1 is not None:
11 $positional_1
12 #end if
13
14 #if $positional_2 and $positional_2 is not None:
15 $positional_2
16 #end if
17
18 > $default]]></command>
19 <inputs>
20 <param area="false" label="bed6 file containing alignments." name="positional_1" type="data" format="bed"/>
21 <param area="false" label="fasta barcode library." name="positional_2" type="data" format="fasta"/>
22 </inputs>
23 <outputs>
24 <data format="bed" hidden="false" name="default"/>
25 </outputs>
26 <tests>
27 <test>
28 <param name="positional_1" value="pcr_dupes_sorted_2.bed"/>
29 <param name="positional_2" value="pcr_dupes_randomdict.fa"/>
30 <output name="default" file="merged_pcr_dupes.bed"/>
31 </test>
32 </tests>
33 <help><![CDATA[
34 Merge PCR duplicates according to random barcode library.
35
36 Barcodes containing uncalled base 'N' are removed.
37
38 Input:
39 * bed6 file containing alignments with fastq read-id in name field
40 * fasta library with fastq read-id as sequence ids
41
42 Output:
43 * bed6 file with random barcode in name field and number of PCR duplicates as score, sorted by fields chrom, start, stop, strand, name
44
45 Author: Daniel Maticzka
46 Copyright: 2015
47 License: Apache
48 Email: maticzkd@informatik.uni-freiburg.de
49 Status: Testing
50 ]]></help>
51 <expand macro="citations" />
52 </tool>