Mercurial > repos > jjohnson > gmap
comparison snpindex.xml @ 11:6adc485b6dc0 draft default tip
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author | jjohnson |
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date | Tue, 31 Jul 2012 08:19:46 -0400 |
parents | 93911bac43da |
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10:93911bac43da | 11:6adc485b6dc0 |
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1 <tool id="gmap_snpindex" name="GMAP SNP Index" version="2.0.0"> | |
2 <description>build index files for known SNPs</description> | |
3 <requirements> | |
4 <requirement type="binary">snpindex</requirement> | |
5 </requirements> | |
6 <version_string>snpindex --version</version_string> | |
7 <command interpreter="command"> /bin/bash $shscript 2>1 1> $output </command> | |
8 <inputs> | |
9 <conditional name="refGenomeSource"> | |
10 <param name="genomeSource" type="select" label="Will you map to a reference genome from your history or use a built-in index?" help="Built-ins were indexed using default options"> | |
11 <option value="indexed">Use a built-in index</option> | |
12 <option value="gmapdb">Use gmapdb from the history</option> | |
13 </param> | |
14 <when value="indexed"> | |
15 <param name="gmapindex" type="select" label="Select a reference genome" help="if your genome of interest is not listed - contact Galaxy team"> | |
16 <options from_file="gmap_indices.loc"> | |
17 <column name="uid" index="0" /> | |
18 <column name="dbkey" index="1" /> | |
19 <column name="name" index="2" /> | |
20 <column name="kmers" index="3" /> | |
21 <column name="maps" index="4" /> | |
22 <column name="snps" index="5" /> | |
23 <column name="value" index="6" /> | |
24 </options> | |
25 </param> | |
26 </when> | |
27 <when value="gmapdb"> | |
28 <param name="gmapdb" type="data" format="gmapdb" metadata_name="dbkey" label="Select a gmapdb" | |
29 help="A GMAP database built with GMAP Build"/> | |
30 </when> | |
31 </conditional> | |
32 <conditional name="dbsnp"> | |
33 <param name="snp_source" type="select" label="Add SNP info from" > | |
34 <option value="snpTable">UCSC SNP Table</option> | |
35 <option value="snpFile">GMAP SNP File</option> | |
36 <option value="snpIIT">"GMAP SNPs map from GMAP iit store</option> | |
37 </param> | |
38 <when value="snpTable"> | |
39 <param name="snps" type="data" format="tabular" label="UCSC SNPs table" help="Example: ftp://hgdownload.cse.ucsc.edu/goldenPath/hg18/database/snp130.txt.gz" /> | |
40 <param name="snpsex" type="data" format="tabular" optional="true" label="UCSC SNP Exceptions table" help="Example: ftp://hgdownload.cse.ucsc.edu/goldenPath/hg18/database/snp130Exceptions.txt.gz" /> | |
41 <param name="weight" type="select" label="Include SNPs with at least Confidence Level" help=""> | |
42 <option value="1" selected="true">1 (High)</option> | |
43 <option value="2">2 (Medium)</option> | |
44 <option value="3">3 (All)</option> | |
45 </param> | |
46 </when> | |
47 <when value="snpFile"> | |
48 <param name="snps" type="data" format="gmap_snps" label="GMAP SNPs file" | |
49 help="Format (3 columns): | |
50 <br>>rs62211261 21:14379270 CG | |
51 <br>>rs62211262 21:14379281 CG | |
52 <br>Each line must start with a > character, then be followed by an | |
53 identifier (which may have duplicates). Then there should be the | |
54 chromosomal coordinate of the SNP. (Coordinates are all 1-based, so | |
55 the first character of a chromosome is number 1.) Finally, there | |
56 should be the two possible alleles: ( AC AG AT CG CT GT or AN CN GN TN) | |
57 <br>These alleles must correspond to the possible nucleotides on the plus strand of the genome. | |
58 If the one of these two letters does not match the allele in the reference | |
59 sequence, that SNP will be ignored in subsequent processing as a probable error. | |
60 The N stands for any other allele." /> | |
61 </when> | |
62 <when value="snpIIT"> | |
63 <param name="snpIIT" type="data" format="snps.iit" label="GMAP SNPs map" help="Created by: GMAP iit store" /> | |
64 </when> | |
65 </conditional> | |
66 <param name="snps_name" type="text" value="snps" label="Name for this SNP index" help="no white space characters"> | |
67 </param> | |
68 </inputs> | |
69 <outputs> | |
70 <!-- | |
71 <data format="txt" name="log" label="${tool.name} on ${on_string}: log"/> | |
72 --> | |
73 <data format="gmapsnpindex" name="output" label="${tool.name} on ${on_string} snpindex" /> | |
74 </outputs> | |
75 <configfiles> | |
76 <configfile name="shscript"> | |
77 #!/bin/bash | |
78 #set $ds = chr(36) | |
79 #set $gt = chr(62) | |
80 #set $lt = chr(60) | |
81 #set $ad = chr(38) | |
82 #import os.path | |
83 #if $refGenomeSource.genomeSource == "gmapdb": | |
84 #set $gmapdb = $refGenomeSource.gmapdb.extra_files_path | |
85 #set $refname = $refGenomeSource.gmapdb.metadata.db_name | |
86 #else: | |
87 #set $gmapdb = $os.path.dirname($refGenomeSource.gmapindex.value) | |
88 $refname = $os.path.basename($refGenomeSource.gmapindex.value) | |
89 #end if | |
90 #set $gmapsnpdir = $output.extra_files_path | |
91 mkdir -p $gmapsnpdir | |
92 #set $snpsname = $snps_name.__str__ | |
93 #set $snpsiit = '.'.join([$snpsname,'iit']) | |
94 #set $pathsnps = $os.path.join($gmapsnpdir,$snpsname) | |
95 #set $pathsnpsiit = $os.path.join($gmapsnpdir,$snpsiit) | |
96 #if $dbsnp.snp_source != 'none' and $dbsnp.snps.__str__ != 'None': | |
97 #if $dbsnp.snp_source == 'snpTable': | |
98 #if $dbsnp.snpsex.__str__ != 'None': | |
99 cat $dbsnp.snps | dbsnp_iit -w $dbsnp.weight -e $dbsnp.snpsex | iit_store -o $pathsnps | |
100 #else: | |
101 cat $dbsnp.snps | dbsnp_iit -w $dbsnp.weight | iit_store -o $pathsnps | |
102 #end if | |
103 #elif $dbsnp.snp_source == 'snpFile': | |
104 cat $dbsnp.snps | iit_store -o $pathsnps | |
105 #elif $dbsnp.snp_source == 'snpIIT': | |
106 cat $dbsnp.snps > $pathsnpsiit | |
107 #end if | |
108 snpindex -D $gmapdb -d $refname -V $output.extra_files_path -v $snpsname $pathsnpsiit | |
109 echo snpindex -D $gmapdb -d $refname -V $output.extra_files_path -v $snpsname $pathsnpsiit | |
110 #end if | |
111 </configfile> | |
112 </configfiles> | |
113 | |
114 <tests> | |
115 </tests> | |
116 | |
117 <help> | |
118 | |
119 | |
120 **GMAP SNP Index** | |
121 | |
122 GMAP SNP Index (snpindex in the GMAP documentaion) creates an index for known SNPs allowing for SNP tolerant mapping and alignment when using GMAP_ (Genomic Mapping and Alignment Program for mRNA and EST sequences) and GSNAP_ (Genomic Short-read Nucleotide Alignment Program). | |
123 | |
124 You will want to read the README_ | |
125 | |
126 Publication_ citation: Thomas D. Wu, Colin K. Watanabe Bioinformatics 2005 21(9):1859-1875; doi:10.1093/bioinformatics/bti310 | |
127 | |
128 .. _GMAP: http://research-pub.gene.com/gmap/ | |
129 .. _GSNAP: http://research-pub.gene.com/gmap/ | |
130 .. _README: http://research-pub.gene.com/gmap/src/README | |
131 .. _Publication: http://bioinformatics.oxfordjournals.org/cgi/content/full/21/9/1859 | |
132 | |
133 | |
134 </help> | |
135 </tool> | |
136 |