--- a/tools/fastq_paired_unpaired/fastq_paired_unpaired.xml	Tue May 16 08:53:57 2017 -0400
+++ b/tools/fastq_paired_unpaired/fastq_paired_unpaired.xml	Fri Apr 16 22:36:15 2021 +0000
@@ -1,5 +1,5 @@
 <tool id="fastq_paired_unpaired" name="Divide FASTQ file into paired and unpaired reads" version="0.1.4">
-    <description>using the read name suffices</description>
+    <description>using the read name suffixes</description>
     <requirements>
         <requirement type="package" version="1.0.1">galaxy_sequence_utils</requirement>
         <requirement type="package" version="1.67">biopython</requirement>
@@ -17,7 +17,7 @@
 $output_singles
     </command>
     <inputs>
-        <param name="input_fastq" type="data" format="fastq" label="FASTQ file to divide into paired and unpaired reads"/>
+        <param name="input_fastq" type="data" format="foobar" label="FASTQ file to divide into paired and unpaired reads"/>
         <conditional name="output_choice_cond">
             <param name="output_choice" type="select" label="How to output paired reads?">
                 <option value="separate">Separate (two FASTQ files, for the forward and reverse reads, in matching order).</option>
@@ -65,7 +65,7 @@
 The input file should be a valid FASTQ file which has been sorted so that
 any partner forward+reverse reads are consecutive. The output files all
 preserve this sort order. Pairing are recognised based on standard name
-suffices. See below or run the tool with no arguments for more details.
+suffixes. See below or run the tool with no arguments for more details.
 
 Any reads where the forward/reverse naming suffix used is not recognised
 are treated as orphan reads. The tool supports the /1 and /2 convention
@@ -75,7 +75,7 @@
 with the fragment number in the description, for example:
 
  * @HWI-ST916:79:D04M5ACXX:1:1101:10000:100326 1:N:0:TGNCCA
- * @HWI-ST916:79:D04M5ACXX:1:1101:10000:100326 2:N:0:TGNCCA 
+ * @HWI-ST916:79:D04M5ACXX:1:1101:10000:100326 2:N:0:TGNCCA
 
 Note that this does support multiple forward and reverse reads per template
 (which is quite common with Sanger sequencing), e.g. this which is sorted
@@ -106,7 +106,7 @@
 Peter J.A. Cock, Björn A. Grüning, Konrad Paszkiewicz and Leighton Pritchard (2013).
 Galaxy tools and workflows for sequence analysis with applications
 in molecular plant pathology. PeerJ 1:e167
-http://dx.doi.org/10.7717/peerj.167
+https://doi.org/10.7717/peerj.167
 
 This tool is available to install into other Galaxy Instances via the Galaxy
 Tool Shed at http://toolshed.g2.bx.psu.edu/view/peterjc/fastq_paired_unpaired