diff raceid_inspectclusters.xml @ 8:2b0d3e2f402a draft default tip

"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/raceid3 commit 455bad7eca54164f95755174904842907846bb42"
author iuc
date Mon, 20 Dec 2021 10:13:54 +0000
parents be4646256624
children
line wrap: on
line diff
--- a/raceid_inspectclusters.xml	Thu Dec 02 16:22:55 2021 +0000
+++ b/raceid_inspectclusters.xml	Mon Dec 20 10:13:54 2021 +0000
@@ -1,4 +1,4 @@
-<tool id="raceid_inspectclusters" name="Cluster Inspection using RaceID" version="@TOOL_VERSION@+galaxy@VERSION_SUFFIX@" >
+<tool id="raceid_inspectclusters" name="Cluster Inspection using RaceID" version="@TOOL_VERSION@+galaxy@VERSION_SUFFIX@" profile="@PROFILE@">
     <description>examines gene expression within clusters</description>
     <macros>
         <import>macros.xml</import>
@@ -37,7 +37,7 @@
     <expand macro="requirements" />
     <expand macro="version_command_config" prog="clusterinspect.R" cheetah="INSPECTCLUSTERS_CHEETAH" out="&#38;&#62; '$outlog'" />
     <inputs>
-        <param name="inputrds" type="data" format="rdata" label="Input RaceID RDS" help="Requires the RDS output from the cluster analysis" />
+        <param name="inputrds" type="data" format="rds" label="Input RaceID RDS" help="Requires the RDS output from the cluster analysis" />
         <conditional name="plotgen">
             <param name="do_opt" type="select" label="Plot Clusters?" help="Generates tSNE and F-R plots" >
                 <option value="yes" selected="true" >Yes</option>
@@ -293,7 +293,7 @@
 
 RaceID is a clustering algorithm for the identification of cell types from single-cell RNA-sequencing data. It was specifically designed for the detection of rare cells which correspond to outliers in conventional clustering methods.
 
-This module inspects the clusters generated from the previous clustering step (and requires the output RData file from it as input).
+This module inspects the clusters generated from the previous clustering step (and requires the output RDS file from it as input).
 
 The tool offers three modes of inspection which can all be activated at the same time, resulting in a single PDF report:
 
@@ -313,7 +313,7 @@
     * The initial and final clustering (as determined using random forest)
     * Heatmaps for each of the most differentially expressed genes in each cluster
 
-The tool requires the RData input from the previous filtering / normalisation / confounder removal step to work.
+The tool requires the RDS input from the previous filtering / normalisation / confounder removal step to work.