diff snpindex.xml @ 11:6adc485b6dc0 draft default tip

Uploaded
author jjohnson
date Tue, 31 Jul 2012 08:19:46 -0400
parents 93911bac43da
children
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--- a/snpindex.xml	Thu Jan 05 14:31:24 2012 -0600
+++ /dev/null	Thu Jan 01 00:00:00 1970 +0000
@@ -1,136 +0,0 @@
-<tool id="gmap_snpindex" name="GMAP SNP Index" version="2.0.0">
-  <description>build index files for known SNPs</description>
-  <requirements>
-      <requirement type="binary">snpindex</requirement>
-  </requirements>
-  <version_string>snpindex --version</version_string>
-  <command interpreter="command"> /bin/bash $shscript 2>1 1> $output </command>
-  <inputs>
-    <conditional name="refGenomeSource">
-     <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">
-        <option value="indexed">Use a built-in index</option>
-        <option value="gmapdb">Use gmapdb from the history</option>
-      </param>
-      <when value="indexed">
-        <param name="gmapindex" type="select" label="Select a reference genome" help="if your genome of interest is not listed - contact Galaxy team">
-          <options from_file="gmap_indices.loc">
-            <column name="uid" index="0" />
-            <column name="dbkey" index="1" />
-            <column name="name" index="2" />
-            <column name="kmers" index="3" />
-            <column name="maps" index="4" />
-            <column name="snps" index="5" />
-            <column name="value" index="6" />
-          </options>
-        </param>
-      </when>
-      <when value="gmapdb">
-        <param name="gmapdb" type="data" format="gmapdb" metadata_name="dbkey" label="Select a gmapdb" 
-              help="A GMAP database built with GMAP Build"/>
-      </when>
-    </conditional>
-    <conditional name="dbsnp">
-      <param name="snp_source" type="select" label="Add SNP info from" >
-        <option value="snpTable">UCSC SNP Table</option>
-        <option value="snpFile">GMAP SNP File</option>
-        <option value="snpIIT">"GMAP SNPs map from GMAP iit store</option>
-      </param>
-      <when value="snpTable">
-        <param name="snps" type="data" format="tabular" label="UCSC SNPs table" help="Example: ftp://hgdownload.cse.ucsc.edu/goldenPath/hg18/database/snp130.txt.gz" />
-        <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" />
-        <param name="weight" type="select" label="Include SNPs with at least Confidence Level" help="">
-          <option value="1" selected="true">1 (High)</option>
-          <option value="2">2 (Medium)</option>
-          <option value="3">3 (All)</option>
-        </param>
-      </when>
-      <when value="snpFile">
-        <param name="snps" type="data" format="gmap_snps" label="GMAP SNPs file" 
-           help="Format (3 columns):
-                &lt;br&gt;>rs62211261 21:14379270 CG
-                &lt;br&gt;>rs62211262 21:14379281 CG
-                &lt;br&gt;Each line must start with a &gt; character, then be followed by an
-                identifier (which may have duplicates).  Then there should be the
-                chromosomal coordinate of the SNP.  (Coordinates are all 1-based, so
-                the first character of a chromosome is number 1.)  Finally, there
-                should be the two possible alleles: ( AC AG AT CG CT GT or AN CN GN TN)
-                &lt;br&gt;These alleles must correspond to the possible nucleotides on the plus strand of the genome.  
-                If the one of these two letters does not match the allele in the reference
-                sequence, that SNP will be ignored in subsequent processing as a probable error.
-                The N stands for any other allele." />
-      </when>
-      <when value="snpIIT">
-        <param name="snpIIT" type="data" format="snps.iit" label="GMAP SNPs map" help="Created by: GMAP iit store" />
-      </when>
-    </conditional> 
-    <param name="snps_name" type="text" value="snps" label="Name for this SNP index" help="no white space characters">
-    </param>
-  </inputs>
-  <outputs>
-    <!--
-    <data format="txt" name="log" label="${tool.name} on ${on_string}: log"/>
-    -->
-    <data format="gmapsnpindex" name="output" label="${tool.name} on ${on_string} snpindex" />
-  </outputs>
-  <configfiles>
-    <configfile name="shscript">
-#!/bin/bash
-#set $ds = chr(36)
-#set $gt = chr(62)
-#set $lt = chr(60)
-#set $ad = chr(38)
-#import os.path
-#if $refGenomeSource.genomeSource == "gmapdb":
-#set $gmapdb = $refGenomeSource.gmapdb.extra_files_path
-#set $refname = $refGenomeSource.gmapdb.metadata.db_name
-#else:
-#set $gmapdb = $os.path.dirname($refGenomeSource.gmapindex.value) 
-$refname = $os.path.basename($refGenomeSource.gmapindex.value)
-#end if
-#set $gmapsnpdir = $output.extra_files_path
-mkdir -p $gmapsnpdir
-#set $snpsname = $snps_name.__str__
-#set $snpsiit = '.'.join([$snpsname,'iit'])
-#set $pathsnps = $os.path.join($gmapsnpdir,$snpsname)
-#set $pathsnpsiit = $os.path.join($gmapsnpdir,$snpsiit)
-#if $dbsnp.snp_source != 'none' and $dbsnp.snps.__str__ != 'None':
-#if $dbsnp.snp_source == 'snpTable':
-#if $dbsnp.snpsex.__str__ != 'None':
-cat $dbsnp.snps | dbsnp_iit -w $dbsnp.weight -e $dbsnp.snpsex | iit_store -o $pathsnps
-#else:
-cat $dbsnp.snps | dbsnp_iit -w $dbsnp.weight | iit_store -o $pathsnps
-#end if
-#elif $dbsnp.snp_source == 'snpFile':
-cat $dbsnp.snps | iit_store -o $pathsnps
-#elif $dbsnp.snp_source == 'snpIIT':
-cat $dbsnp.snps  > $pathsnpsiit
-#end if
-snpindex -D $gmapdb -d $refname -V $output.extra_files_path -v $snpsname $pathsnpsiit
-echo snpindex -D  $gmapdb -d $refname -V $output.extra_files_path -v $snpsname $pathsnpsiit
-#end if
-    </configfile>
-  </configfiles>
-
-  <tests>
-  </tests> 
-
-  <help>
-
-
-**GMAP SNP Index**
-
-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).  
-
-You will want to read the README_
-
-Publication_ citation: Thomas D. Wu, Colin K. Watanabe  Bioinformatics 2005 21(9):1859-1875; doi:10.1093/bioinformatics/bti310
-
-.. _GMAP: http://research-pub.gene.com/gmap/
-.. _GSNAP: http://research-pub.gene.com/gmap/
-.. _README: http://research-pub.gene.com/gmap/src/README
-.. _Publication: http://bioinformatics.oxfordjournals.org/cgi/content/full/21/9/1859
-
-
-  </help>
-</tool>
-