comparison dividePgSnpAlleles.xml @ 2:35c20b109be5

Retrying upload with "bare" tarball (i.e. one without a top containing directory).
author cathy
date Tue, 28 May 2013 17:54:02 -0400
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1:1d8b23a21735 2:35c20b109be5
1 <tool id="dividePgSnp" name="Separate pgSnp Alleles" version="1.1.0" hidden="false">
2 <description>: Split allele info into separate columns</description>
3 <command interpreter="perl">
4 #if $refcol.ref == "yes" #dividePgSnpAlleles.pl -ref=$refcol.ref_column $input1 > $out_file1
5 #else #dividePgSnpAlleles.pl $input1 > $out_file1
6 #end if
7 </command>
8 <inputs>
9 <param format="interval" name="input1" type="data" label="pgSnp dataset" />
10 <conditional name="refcol">
11 <param name="ref" type="select" label="Dataset has a column with the reference allele">
12 <option value="yes">yes</option>
13 <option value="no" selected="true">no</option>
14 </param>
15 <when value="yes">
16 <param name="ref_column" type="data_column" data_ref="input1" label="Column with reference allele" />
17 </when>
18 <when value="no"> <!-- do nothing -->
19 </when>
20 </conditional>
21 </inputs>
22 <outputs>
23 <data format="interval" name="out_file1" />
24 </outputs>
25 <tests>
26 <test>
27 <param name='input1' value='dividePgSnp_input.pgSnp' ftype='interval' />
28 <param name='refcol' value='no' />
29 <output name="output" file="dividePgSnp_output.txt" />
30 </test>
31 </tests>
32
33 <help>
34
35 **Dataset formats**
36
37 The input dataset is of Galaxy datatype interval_, with the additional columns
38 required for pgSnp_ format.
39 Any further columns beyond those defined for pgSnp will be appended to the output.
40 The output dataset is in interval_ format. (`Dataset missing?`_)
41
42 .. _interval: ./static/formatHelp.html#interval
43 .. _pgSnp: ./static/formatHelp.html#pgSnp
44 .. _Dataset missing?: ./static/formatHelp.html
45
46 -----
47
48 **What it does**
49
50 This separates the alleles from a pgSnp dataset into separate columns,
51 and also the frequencies and scores that go with the alleles. It will skip
52 any positions with more than 2 alleles. If only a single allele is given then "N"
53 will be used for the second, with a frequency and score of zero. Or, if a
54 column with reference alleles is provided,
55 the value in that column will be used in place of the "N".
56
57 -----
58
59 **Example**
60
61 - input pgSnp file::
62
63 chr1 256 257 A/C 2 3,4 10,20
64 chr1 56100 56101 A 1 5 30
65 chr1 77052 77053 A/G 2 6,7 40,50
66 chr1 110904 110905 A 1 8 60
67 etc.
68
69 - output::
70
71 chr1 256 257 A 3 10 C 4 20
72 chr1 56100 56101 A 5 30 N 0 0
73 chr1 77052 77053 A 6 40 G 7 50
74 chr1 110904 110905 A 8 60 N 0 0
75 etc.
76
77 </help>
78 </tool>