Mercurial > repos > wolma > mimodd_core
comparison covstats.xml @ 0:aa82b2e54055 draft
planemo upload for repository https://github.com/wm75/mimodd_galaxy_wrappers commit b36048cd608ede0ec6f6559648525c9350caae34-dirty
author | wolma |
---|---|
date | Sat, 11 Nov 2017 18:19:22 -0500 |
parents | |
children |
comparison
equal
deleted
inserted
replaced
-1:000000000000 | 0:aa82b2e54055 |
---|---|
1 <tool id="mimodd_covstats" name="MiModD Coverage Statistics" | |
2 version="@MIMODD_WRAPPER_VERSION@"> | |
3 <description> | |
4 calculates coverage statistics for a BCF file as generated by the MiModd Variant Calling tool | |
5 </description> | |
6 <macros> | |
7 <import>macros.xml</import> | |
8 </macros> | |
9 <expand macro="requirements" /> | |
10 <expand macro="stdio" /> | |
11 <expand macro="version_command" /> | |
12 <command><![CDATA[ | |
13 mimodd covstats '$ifile' --ofile '$ofile' | |
14 ]]></command> | |
15 | |
16 <inputs> | |
17 <param name="ifile" type="data" format="bcf" label="BCF input file" | |
18 help="Use the Variant Calling tool to generate input for this tool."/> | |
19 </inputs> | |
20 <outputs> | |
21 <data name="ofile" format="tabular" | |
22 label="Coverage Statistics for ${on_string}"/> | |
23 </outputs> | |
24 | |
25 <tests> | |
26 <test> | |
27 <param name="ifile" value="a.bcf" /> | |
28 <output name="ofile" ftype="tabular"> | |
29 <assert_contents> | |
30 <has_n_columns n="3" /> | |
31 <has_line_matching expression="^chrI	.+" /> | |
32 <has_line_matching expression="^chrII	.+" /> | |
33 <has_line_matching expression="^chrIII	.+" /> | |
34 <has_line_matching expression="^chrIV	.+" /> | |
35 <has_line_matching expression="^chrV	.+" /> | |
36 <has_line_matching expression="^chrX	.+" /> | |
37 <has_line_matching expression="^MtDNA	.+" /> | |
38 </assert_contents> | |
39 </output> | |
40 </test> | |
41 </tests> | |
42 | |
43 <help><![CDATA[ | |
44 .. class:: infomark | |
45 | |
46 **What it does** | |
47 | |
48 The tool takes as input a BCF file produced by the *Variant Calling* tool, and calculates per-chromosome read coverage from it. | |
49 | |
50 .. class:: warningmark | |
51 | |
52 The tool treats genome positions missing from the BCF input as zero coverage, so it is safe to use ONLY with BCF files produced by the *Variant Calling* tool or through other commands that keep the information for all sites. | |
53 | |
54 @HELP_FOOTER@ | |
55 ]]></help> | |
56 <expand macro="citations" /> | |
57 </tool> |