comparison pgSnp2gd_snp.xml @ 1:4cd611004dc4 draft default tip

planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/pgsnp2gd_snp commit a1517c9d22029095120643bbe2c8fa53754dd2b7
author devteam
date Wed, 11 Nov 2015 12:22:57 -0500
parents d281062566f9
children
comparison
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0:d281062566f9 1:4cd611004dc4
1 <tool id="pgSnp2gd_snp" name="pgSnp to gd_snp" hidden="false" version="1.0.0"> 1 <tool id="pgSnp2gd_snp" name="pgSnp to gd_snp" hidden="false" version="1.0.0">
2 <description>Convert from pgSnp to gd_snp</description> 2 <description>Convert from pgSnp to gd_snp</description>
3 <command interpreter="perl"> 3 <command interpreter="perl">
4 #if $snptab.tab2 == "yes" 4 <![CDATA[
5 #if $snptab.colsOnly == "addColsOnly" #pgSnp2gd_snp.pl $input1 -tab=$snptab.input2 -name=$indName -build=${input1.metadata.dbkey} -addColsOnly -chr=${input1.metadata.chromCol} > $out_file1 5 #if $snptab.tab2 == "yes"
6 #else #pgSnp2gd_snp.pl $input1 -tab=$snptab.input2 -name=$indName -build=${input1.metadata.dbkey} -ref=${ref} -chr=${input1.metadata.chromCol} > $out_file1 6 #if $snptab.needRef.colsOnly == "addColsOnly"
7 #end if 7 pgSnp2gd_snp.pl '$input1' -tab=${snptab.input2} -name=$indName -build=${input1.metadata.dbkey} -addColsOnly -chr=${input1.metadata.chromCol} > '$out_file1'
8 #else #pgSnp2gd_snp.pl $input1 -name=$indName -build=${input1.metadata.dbkey} -ref=${ref} -chr=${input1.metadata.chromCol} > $out_file1 8 #else
9 pgSnp2gd_snp.pl '$input1' -tab=${snptab.input2} -name=$indName -build=${input1.metadata.dbkey} -ref=${snptab.needRef.ref} -chr=${input1.metadata.chromCol} > '$out_file1'
9 #end if 10 #end if
10 </command> 11 #else
11 <inputs> 12 pgSnp2gd_snp.pl '$input1' -name=$indName -build=${input1.metadata.dbkey} -ref=${snptab.ref} -chr=${input1.metadata.chromCol} > '$out_file1'
12 <param format="tab" name="input1" type="data" label="pgSnp dataset" /> 13 #end if
13 <conditional name="snptab"> 14 ]]>
14 <param name="tab2" type="select" label="Append to gd_snp dataset in history"> 15 </command>
15 <option value="yes">yes</option> 16 <inputs>
16 <option value="no" selected="true">no</option> 17 <param format="tab" name="input1" type="data" label="pgSnp dataset" />
17 </param> 18 <conditional name="snptab">
18 <when value="yes"> 19 <param name="tab2" type="select" label="Append to gd_snp dataset in history">
19 <param format="gd_snp" name="input2" type="data" label="gd_snp dataset" /> 20 <option value="yes">yes</option>
20 <conditional name="needRef"> 21 <option value="no" selected="true">no</option>
21 <param name="colsOnly" type="select" label="Skip new SNPs"> 22 </param>
22 <option value="no" selected="true">no</option> 23 <when value="yes">
23 <option value="addColsOnly">yes</option> 24 <param format="gd_snp" name="input2" type="data" label="gd_snp dataset" />
24 </param> 25 <conditional name="needRef">
25 <when value="no"> 26 <param name="colsOnly" type="select" label="Skip new SNPs">
26 <param name="ref" type="data_column" data_ref="input1" label="Column with reference allele" /> 27 <option value="no" selected="true">no</option>
27 </when> 28 <option value="addColsOnly">yes</option>
28 <when value="addColsOnly"> <!-- do nothing --> 29 </param>
29 </when> 30 <when value="no">
31 <param name="ref" type="data_column" data_ref="input1" label="Column with reference allele" />
32 </when>
33 <when value="addColsOnly" />
34 </conditional>
35 </when>
36 <when value="no">
37 <param name="ref" type="data_column" data_ref="input1" label="Column with reference allele" />
38 </when>
30 </conditional> 39 </conditional>
31 </when> 40 <param name="indName" type="text" label="Label for new individual/group" value="na" />
32 <when value="no"> 41 </inputs>
33 <param name="ref" type="data_column" data_ref="input1" label="Column with reference allele" /> 42 <outputs>
34 </when> 43 <data format="gd_snp" name="out_file1" />
35 </conditional> 44 </outputs>
36 <param name="indName" type="text" size="20" label="Label for new individual/group" value="na" /> 45 <tests>
37 </inputs> 46 <test>
38 <outputs> 47 <param name="input1" value="pgSnpTest.ref.txt" ftype="interval" dbkey="hg19" />
39 <data format="gd_snp" name="out_file1" /> 48 <param name="tab2" value="no" />
40 </outputs> 49 <param name="ref" value="8" />
41 <tests> 50 <param name="indName" value="na" />
42 <test> 51 <output name="output" file="pgSnp2snp_output.txt" />
43 <param name='input1' value='pgSnpTest.ref.txt' ftype='interval' /> 52 </test>
44 <param name='tab2' value='no' /> 53 </tests>
45 <param name='ref' value='8' />
46 <param name='indName' value='na' />
47 <output name="output" file="pgSnp2snp_output.txt" />
48 </test>
49 </tests>
50 54
51 <help> 55 <help>
52
53 **Dataset formats** 56 **Dataset formats**
54 57
55 The input dataset is of Galaxy datatype interval_, with the additional columns 58 The input dataset is of Galaxy datatype interval_, with the additional columns
56 required for pgSnp_ format. 59 required for pgSnp_ format.
57 Any further columns beyond those defined for pgSnp will be ignored. 60 Any further columns beyond those defined for pgSnp will be ignored.
67 **What it does** 70 **What it does**
68 71
69 This tool converts a pgSnp dataset to gd_snp format, either starting a new 72 This tool converts a pgSnp dataset to gd_snp format, either starting a new
70 dataset or appending to an old one. When appending, 73 dataset or appending to an old one. When appending,
71 if any new SNPs appear only in the pgSnp file they can either be skipped entirely, or 74 if any new SNPs appear only in the pgSnp file they can either be skipped entirely, or
72 backfilled with "-1" (meaning "unknown") for previous individuals/groups in the 75 backfilled with "-1" (meaning "unknown") for previous individuals/groups in the
73 input gd_snp dataset. 76 input gd_snp dataset.
74 If any new SNPs are being added (either by creating a new table or by backfilling), 77 If any new SNPs are being added (either by creating a new table or by backfilling),
75 then an extra column with the reference allele must be supplied in the pgSnp dataset, 78 then an extra column with the reference allele must be supplied in the pgSnp dataset,
76 as shown in the example below. 79 as shown in the example below.
77 80
90 93
91 chr1 1888681 T C -1 3 4 1 0.8893 94 chr1 1888681 T C -1 3 4 1 0.8893
92 chr1 3118325 C T -1 0 8 0 0.8796 95 chr1 3118325 C T -1 0 8 0 0.8796
93 chr1 3211457 A C -1 17 10 1 0.8576 96 chr1 3211457 A C -1 17 10 1 0.8576
94 etc. 97 etc.
95 98 </help>
96 </help>
97 </tool> 99 </tool>