# HG changeset patch
# User melissacline
# Date 1423721730 18000
# Node ID 6c23a3b58eb819698dc742e98757e4b8338770f4
# Parent  60efb9214eaa020c5870f51b7e66efafeb0eb10a
Uploaded

diff -r 60efb9214eaa -r 6c23a3b58eb8 mergeGenomicFiles.xml
--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/mergeGenomicFiles.xml	Thu Feb 12 01:15:30 2015 -0500
@@ -0,0 +1,20 @@
+<tool id="mergeGenomicFiles" description="Merge two genomic datasets into a new dataset" name="mergeGenomicFiles" version="0.0.1">
+  <description>
+    Given two genomic datasets, merge them to create a third dataset with the row and column identifiers from both datasets.
+  </description>
+  <command interpreter="python">
+      mergeGenomicMatrixFiles.py $outputC $inputA $inputB
+  </command>
+  <inputs>
+    <param name="inputA" format="tabular" type="data" label="Genomic Dataset A"/>
+    <param name="inputB" format="tabular" type="data" label="Genomic Dataset B"/>
+  </inputs>
+  <outputs>
+    <data name="outputC" format="tabular"/>
+  </outputs>
+  <help>
+    ***Merge Genomic Datasets***
+
+    Given two genomic datasets, merge them to produce a third dataset that is the union of the first two.  The new dataset will contain all column labels from either dataset, and all row labels from either dataset.  If a row label appears in both datasets, the output dataset will contain, for that row, all values for the first set of columns, plus all values for the second set of columns.  If a row label appears in the first dataset only, the output dataset will contain the values for the columns of the first dataset, and blanks (indicating missing values) for the columns of the second da
+  </help>
+</tool>