Try separator in groovy

scripts/make_config_file.groovy

@@ -28,14 +28,14 @@ pipeline {
         booleanParam(name: 'COLLAPSE', defaultValue: true, description: 'Collapse replicates.')
         booleanParam(name: 'REMOVE_DATA', defaultValue: false, description: 'Select if there is experimental data that needs to be removed prior to normalization.')
         booleanParam(name: 'CONVERT_SUSHI', defaultValue: false, description: 'Convert output column headers to format for MTS pipeline and upload to s3.')
-        booleanParam(name: 'RUN_EPS_QC', defaultValue: false, description: 'Run EPS QC')
-        string(name: 'BUILD_DIR', defaultValue: '/cmap/obelix/pod/prismSeq/', description: 'Output path to deposit build. Format should be /directory/PROJECT_CODE/BUILD_NAME')
+        string(name: 'DAYS', defaultValue: '', description: 'If running the sushi_to_mts module, provide any days/timepoints (separated by commas) that should be dropped from output data. No quotes needed (ie, 2,8).')
+        booleanParam(name: 'RUN_EPS_QC', defaultValue: false, description: 'Generates an EPS specific QC report.')
+        string(name: 'BUILD_DIR', defaultValue: '/cmap/obelix/pod/prismSeq/', description: 'Output path to deposit build files. Format should be /directory/PROJECT_CODE/BUILD_NAME')
         string(name: 'BUILD_NAME', defaultValue: '', description: 'Build name, files will start with this prefix.')
         string(name: 'SEQ_TYPE', defaultValue: 'DRAGEN', description: 'Choose DRAGEN, MiSeq, HiSeq, or NovaSeq. MiSeq and HiSeq/NovaSeq return files named differently. This setting sets the INDEX_1, INDEX_2, and BARCODE_SUFFIX parameters in fastq2readcount. Select DRAGEN if fastq files are from the DRAGEN pipeline from GP. Choosing NovaSeq reverses index 2.')
-        string(name: 'CTL_TYPES', defaultValue: 'negcon', description: 'Type to mark as control in compute_LFC')
-        string(name: 'SIG_COLS', defaultValue: 'cell_set,treatment,dose,dose_unit,day', description: 'Columns that ecode all experimental conditions')
+        string(name: 'SIG_COLS', defaultValue: 'cell_set,treatment,dose,dose_unit,day', description: 'Columns that encode all experimental conditions')
+        string(name: 'CTL_TYPES', defaultValue: 'negcon', description: 'Perturbation type to mark as negative control when computing fold changes.')
         string(name: 'CONTROL_COLS', defaultValue: 'cell_set,day', description: 'Set of columns that define individual controls; should be a subset of SIG_COLS')
-        string(name: 'DAYS', defaultValue: '', description: 'If running the sushi_to_mts module, provide any days/timepoints (separated by commas) that should be dropped from output data. No quotes needed (ie, 2,8).')
         separator(
           name: "Group_1",
           sectionHeader: "Do Not Edit",