--- a/cfsan_centriflaken.xml	Thu Jul 07 10:37:59 2022 -0400
+++ b/cfsan_centriflaken.xml	Mon Jul 11 12:19:48 2022 -0400
@@ -43,8 +43,7 @@
 	--fq_filename_delim '${fq_filename_delim}'
 	--fq_filename_delim_idx $fq_filename_delim_idx
 	--centrifuge_extract_bug '${centrifuge_extract_bug}'
-	-profile $runtime_profile
-    -resume;
+	-profile kondagac;
     mv './cpipes-output/${pipeline}-multiqc/multiqc_report.html' './multiqc_report.html';
     mv './cpipes-output/${pipeline}-results/kraken2_extract_contigs' kraken2_extract_contigs;
     rm -rf ./cpipes-output;
@@ -72,7 +71,8 @@
             <option value="pacbio_hifi">PacBio HiFi reads (&lt;1% error)</option>
         </param>
         <param name="fq_suffix" value=".fastq.gz" type="text" label="Suffix of the R1 FASTQ or Unpaired FASTQ"/>
-        <param name="fq2_suffix" value="_R2_001.fastq.gz" type="text" label="Suffix of the R2 FASTQ"/>
+        <param name="fq2_suffix" value="_R2_001.fastq.gz" type="text" label="Suffix of the R2 FASTQ"
+            help="THIS OPTION IS IGNORED IF THE INPUT READS ARE UNPAIRED/LONG READS."/>
         <param name="fq_filter_by_len" optional="true" value="" type="integer" label="Enter minimum read length to retain before starting the analysis"
             help="Keep this option empty to use default values. Default for centriflaken (long reads) is 4000 bp and for centriflaken_hy (short reads) is 75 bp)"/>
         <param name="fq_filename_delim" type="text" value="_" label="File name delimitor by which samples are grouped together (--fq_filename_delim)" 
@@ -82,10 +82,10 @@
         <param name="genome_size" type="text" optional="true" value="5.5m" label="Estimated genome size" help="For example, 5m or 2.6g.">
             <validator type="regex" message="Genome size must be a float  or integer, optionally followed by the a unit prefix (kmg)">^([0-9]*[.])?[0-9]+[kmg]?$</validator>
         </param>
-        <param name="runtime_profile" type="select" label="Run time profile">
+        <!-- <param name="runtime_profile" type="select" label="Run time profile">
             <option value="kondagac" selected="true">conda</option>
             <option value="cingularitygac">singularity</option>
-        </param>
+        </param> -->
     </inputs>
     <outputs>
         <data name="multiqc_report" format="html" label="${pipeline}: MultiQC Report on ${on_string}" from_work_dir="multiqc_report.html"/>
@@ -124,11 +124,11 @@
 
 **Testing and Validation**
 
-The pipeline has been wrapped to make it work in Galaxy. It takes in either paired or unpaired short reads or long reads, generates MAGs and performs 
+The CPIPES - Centriflaken Nextflow pipeline has been wrapped to make it work in Galaxy. It takes in either paired or unpaired short reads or long reads, generates MAGs and performs 
 in silico-based analysis (i.e., virulence gene finding). Additionally, AMR gene finding analysis is also included in Centriflaken and performed on MAGs 
 of interest. The final summary plots and tables can be downloaded from the provided MultiQC HTML report generated as part of the pipeline. 
 The Centriflaken pipeline was validated with data from our previously published method (Maguire et al, 2021) and was able to replicate the detection 
-and classification of STECs for each sample. We tested the pipeline with nanopore data obtained from 21 additional enriched samples from 
+and classification of STECs for each sample. We tested the pipeline with Nanopore data obtained from 21 additional enriched samples from 
 irrigation water and was able to perform the entire precision metagenomics analysis in less than 5 hours for all of them. All the original testing and validation was 
 done on the command line on the CFSAN Raven2 HPC Cluster.