changeset 1:7c95db468ad5

Uploaded xml
author nick
date Fri, 24 May 2013 08:55:29 -0400
parents 57e85db3f13c
children d83368b907f7
files allele-counts.xml
diffstat 1 files changed, 24 insertions(+), 0 deletions(-) [+]
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--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/allele-counts.xml	Fri May 24 08:55:29 2013 -0400
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+<tool id="allele_counts_1" version="1.0" name="Count alleles">
+  <description>and minor allele frequencies</description>
+  <command interpreter="python">allele-counts.py -i $input -o $output -f $freq -c $covg $header</command>
+  <inputs>
+    <param name="input" type="data" format="vcf" label="Input variants from Naive Variants Detector"/>
+    <param name="freq" type="float" value="1.0" min="0" max="100" label="Minor allele frequency threshold"/>
+    <param name="covg" type="integer" value="10" min="0" label="Coverage threshold (per strand)"/>
+    <param name="header" type="boolean" truevalue="-H" falsevalue="" checked="False" label="Write header line" />
+  </inputs>
+  <outputs>
+    <data name="output" format="tabular"/>
+  </outputs>
+  <stdio>
+    <exit_code range="1:" err_level="fatal"/>
+    <exit_code range=":-1" err_level="fatal"/>
+  </stdio>
+
+  <help>
+This tool parses the output of Naive Variant Detector, counting variants, calculating numbers of alleles, and minor allele frequency. It applies filters based on coverage, strand bias, and minor allele frequency cutoffs.
+
+**Note**: The VCF file from the Naive Variant Detector must include counts *per strand*.
+  </help>
+
+</tool>
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