diff varscan/varscan_somatic.native.xml @ 0:848f3dc54593 draft

Uploaded

--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/varscan/varscan_somatic.native.xml	Fri Mar 07 06:17:32 2014 -0500
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+<tool id="varscan_somatic" name="VarScan Somatic (Native Output)" version="2.3.5">
+  <description>
+        somatic mutation caller for cancer genomics
+  </description>
+  <requirements>
+  	<requirement type="package" version="2.3.5">VarScan</requirement>
+  </requirements>
+  <command interpreter="perl">
+  	
+	varscan_somatic.pl 
+  	"COMMAND::java -jar \$JAVA_JAR_PATH/VarScan.v2.3.5.jar somatic" 
+  	"NORMAL::$normal" 
+  	"TUMOR::$tumor"
+	"TUMORBAM::$tumorbam"
+	"SNP::$snp"
+	"INDEL::$indel"
+        "LOG::$log"
+  	
+	"OPTION::--min-coverage $min_coverage"
+	"OPTION::--min-coverage-normal $min_coverage_normal"
+	"OPTION::--min-coverage-tumor $min_coverage_tumor"
+	
+	"OPTION::--min-var-freq $min_var_freq"
+	"OPTION::--min-freq-for-hom $min_freq_for_hom"
+	
+	"OPTION::--normal-purity $normal_purity"	
+	"OPTION::--tumor-purity $tumor_purity"		
+	
+	"OPTION::--p-value $p_value"	
+	"OPTION::--somatic-p-value $somatic_p_value"	
+
+	"OPTION::--strand-filter $strand_filter"	
+	"OPTION::--validation $validation"	
+	
+
+  	
+  </command>
+
+  <inputs>
+
+	<param name="normal" type="data" format="pileup" label="normal mpileup file" help="The SAMtools mpileup file for normal sample" />
+	<param name="tumor" type="data" format="pileup" label="tumor mpileup file" help="The SAMtools mpileup file for tumor sample" />
+	<param name="tumorbam" type="data" format="bam" label="tumor BAM file" help="The BAM file of the tumor sample used in mpileup step" />
+
+	<param name="min_coverage" type="integer" label="min-coverage" help="" optional="true" value="8"/>
+	<param name="min_coverage_normal" type="integer" label="min-coverage-normal" help="" optional="true" value="8"/>
+	<param name="min_coverage_tumor" type="integer" label="min-coverage-tumor" help="" optional="true" value="6"/>
+	
+	<param name="min_var_freq" type="float" label="min-var-freq" help="" optional="true" value="0.10"/>
+	<param name="min_freq_for_hom" type="float" label="min-freq-for-hom" help="" optional="true" value="0.75"/>
+	
+	<param name="normal_purity" type="float" label="normal-purity" help="" optional="true" value="1.00"/>
+	<param name="tumor_purity" type="float" label="tumor-purity" help="" optional="true" value="1.00"/>
+	
+
+	<param name="p_value" type="text" label="p-value" help="" optional="true" value="0.99"/>
+	<param name="somatic_p_value" type="text" label="somatic-p-value" help="" optional="true" value="0.05"/>
+
+	<param name="strand_filter" type="integer" label="strand-filter" help="" optional="true" value="1"/>
+	<param name="validation" type="integer" label="validation" help="" optional="true" value="0"/>
+	
+  </inputs>
+  <outputs>
+        <data type="data" format="txt" name="log" label="${tool.name} result on ${on_string} (log) "/>
+	<data type="data" format="txt" name="snp" label="${tool.name} result on ${on_string} (SNP)" />
+	<data type="data" format="txt" name="indel" label="${tool.name} result on ${on_string} (INDEL)" />
+	
+
+  </outputs>
+  	
+  <help> 
+
+.. class:: infomark
+
+**What it does**
+
+::
+
+ VarScan is a platform-independent mutation caller for targeted, exome, and whole-genome resequencing data generated on Illumina, SOLiD, Life/PGM, Roche/454, and similar instruments. The newest version, VarScan 2, is written in Java, so it runs on most  operating systems. It can be used to detect different types of variation:
+
+    Germline variants (SNPs an dindels) in individual samples or pools of samples.
+    Multi-sample variants (shared or private) in multi-sample datasets (with mpileup).
+    Somatic mutations, LOH events, and germline variants in tumor-normal pairs.
+    Somatic copy number alterations (CNAs) in tumor-normal exome data.
+
+
+**Input**
+
+::
+
+  mpileup normal file - The SAMtools mpileup file for normal
+  mpileup tumor file - The SAMtools mpileup file for tumor
+ 
+
+**Parameters**
+
+::
+
+  min-coverage	
+  	Minimum read depth at a position to make a call [8]
+
+  min-coverage-normal	
+  	Minimum coverage in normal to call somatic [8]
+  	
+  min-coverage-tumor	
+  	Minimum coverage in tumor to call somatic [6]
+  	
+  min-var-freq 
+  	Minimum variant frequency to call a heterozygote [0.10]  	  	
+
+  min-freq-for-hom
+  	Minimum frequency to call homozygote [0.75]
+  	
+  normal-purity 
+  	Estimated purity (non-tumor content) of normal sample [1.00]
+  	
+  tumor-purity
+  	Estimated purity (tumor content) of tumor sample [1.00]
+  
+  p-value
+  	Default p-value threshold for calling variants [0.99]
+  	
+  somatic-p-value
+  	P-value threshold to call a somatic site [0.05]  	
+  
+  strand-filter
+  	If set to 1, removes variants with >90% strand bias
+  	
+  validation 
+  	If set to 1, outputs all compared positions even if non-variant
+  
+  output-vcf
+  	If set to 1, outputs in VCF format [Default]
+
+
+  
+  </help>
+</tool>
+