diff --git a/tools/fasta_filter_by_id/README.rst b/tools/fasta_filter_by_id/README.rst
index 2ed61bc..5be35b9 100644
--- a/tools/fasta_filter_by_id/README.rst
+++ b/tools/fasta_filter_by_id/README.rst
@@ -53,6 +53,7 @@ v0.0.5  - Explicit dependency on ``galaxy_sequence_utils``.
         - Use standard MIT license (was previously using the MIT/BSD style
           Biopython Licence Agreement).
 v0.0.6  - Python 3 compatible print function.
+v0.0.7  - Fix file open mode for Python 3.11 onwards.
 ======= ======================================================================
 
 
diff --git a/tools/fasta_filter_by_id/fasta_filter_by_id.py b/tools/fasta_filter_by_id/fasta_filter_by_id.py
index 066d7a0..2519a8e 100644
--- a/tools/fasta_filter_by_id/fasta_filter_by_id.py
+++ b/tools/fasta_filter_by_id/fasta_filter_by_id.py
@@ -16,7 +16,7 @@
 in column one, and the ID of the match from the database is in column two.
 Here sensible values for the column numbers would therefore be "1" or "2".
 
-This tool is copyright 2010-2017 by Peter Cock, The James Hutton Institute
+This tool is copyright 2010-2023 by Peter Cock, The James Hutton Institute
 (formerly SCRI, Scottish Crop Research Institute), UK. All rights reserved.
 See accompanying text file for licence details (MIT license).
 """
@@ -26,7 +26,7 @@
 import sys
 
 if "-v" in sys.argv or "--version" in sys.argv:
-    print("v0.0.6")
+    print("v0.0.7")
     sys.exit(0)
 
 from galaxy_utils.sequence.fasta import fastaReader, fastaWriter
diff --git a/tools/fasta_filter_by_id/fasta_filter_by_id.xml b/tools/fasta_filter_by_id/fasta_filter_by_id.xml
index 3d0823c..25bd642 100644
--- a/tools/fasta_filter_by_id/fasta_filter_by_id.xml
+++ b/tools/fasta_filter_by_id/fasta_filter_by_id.xml
@@ -1,4 +1,4 @@
-<tool id="fasta_filter_by_id" name="Filter FASTA by ID" version="0.0.6" hidden="true">
+<tool id="fasta_filter_by_id" name="Filter FASTA by ID" version="0.0.7" hidden="true">
     <description>from a tabular file</description>
     <requirements>
         <requirement type="package" version="1.0.1">galaxy_sequence_utils</requirement>
diff --git a/tools/predictnls/README.rst b/tools/predictnls/README.rst
index 0b012e3..ddf6753 100644
--- a/tools/predictnls/README.rst
+++ b/tools/predictnls/README.rst
@@ -70,6 +70,7 @@ v0.0.9  - Use ``<command detect_errors="aggressive">`` (internal change only).
         - Single quote command line arguments (internal change only).
         - Python 3 compatible print function.
         - Record version of the Python script.
+v0.0.10 - Fix file open mode for Python 3.11 onwards.
 ======= ======================================================================
 
 
diff --git a/tools/predictnls/predictnls.py b/tools/predictnls/predictnls.py
index 523de36..2ff3708 100755
--- a/tools/predictnls/predictnls.py
+++ b/tools/predictnls/predictnls.py
@@ -1,6 +1,6 @@
 #!/usr/bin/env python
 
-# Copyright 2011-2013 by Peter Cock, James Hutton Institute (formerly SCRI), UK
+# Copyright 2011-2023 by Peter Cock, James Hutton Institute (formerly SCRI), UK
 #
 # Licenced under the GPL (GNU General Public Licence) version 3.
 #
@@ -56,7 +56,7 @@
 import sys
 
 if "-v" in sys.argv or "--version" in sys.argv:
-    print("v0.0.9")
+    print("v0.0.10")
     sys.exit(0)
 
 if len(sys.argv) == 4:
diff --git a/tools/predictnls/predictnls.xml b/tools/predictnls/predictnls.xml
index 95975f5..8e145e4 100644
--- a/tools/predictnls/predictnls.xml
+++ b/tools/predictnls/predictnls.xml
@@ -1,4 +1,4 @@
-<tool id="predictnls" name="PredictNLS" version="0.0.9">
+<tool id="predictnls" name="PredictNLS" version="0.0.10">
     <description>Find nuclear localization signals (NLSs) in protein sequences</description>
     <version_command>
 python $__tool_directory__/predictnls.py --version
diff --git a/tools/seq_primer_clip/README.rst b/tools/seq_primer_clip/README.rst
index 163e744..302237e 100644
--- a/tools/seq_primer_clip/README.rst
+++ b/tools/seq_primer_clip/README.rst
@@ -1,7 +1,7 @@
 Galaxy tool to primer clip (trim) FASTA, FASTQ or SFF reads
 ===========================================================
 
-This tool is copyright 2011-2017 by Peter Cock, The James Hutton Institute
+This tool is copyright 2011-2023 by Peter Cock, The James Hutton Institute
 (formerly SCRI, Scottish Crop Research Institute), UK. All rights reserved.
 See the licence text below (MIT licence).
 
@@ -74,6 +74,8 @@ v0.0.14 - Depends on Biopython 1.67 via legacy Tool Shed package or bioconda.
 v0.0.15 - Use ``<command detect_errors="aggressive">`` (internal change only).
         - Single quote command line arguments (internal change only)
 v0.0.16 - Python 3 compatible print function.
+v0.0.17 - Use Python 3 style dictionary iteration.
+v0.0.18 - Fix file open mode for Python 3.11 onwards.
 ======= ======================================================================
 
 
diff --git a/tools/seq_primer_clip/seq_primer_clip.py b/tools/seq_primer_clip/seq_primer_clip.py
index e313b84..4a799a2 100644
--- a/tools/seq_primer_clip/seq_primer_clip.py
+++ b/tools/seq_primer_clip/seq_primer_clip.py
@@ -22,7 +22,7 @@
 Note that only the trim/clip values in the SFF file are changed, not the flow
 information of the full read sequence.
 
-This script is copyright 2011-2013 by Peter Cock, The James Hutton Institute
+This script is copyright 2011-2023 by Peter Cock, The James Hutton Institute
 (formerly the Scottish Crop Research Institute, SCRI), UK. All rights reserved.
 See accompanying text file for licence details (MIT/BSD style).
 
@@ -34,7 +34,7 @@
 import sys
 
 if "-v" in sys.argv or "--version" in sys.argv:
-    print("v0.0.17")
+    print("v0.0.18")
     sys.exit(0)
 
 from galaxy_utils.sequence.fasta import fastaReader, fastaWriter
diff --git a/tools/seq_primer_clip/seq_primer_clip.xml b/tools/seq_primer_clip/seq_primer_clip.xml
index 45f8780..72995e4 100644
--- a/tools/seq_primer_clip/seq_primer_clip.xml
+++ b/tools/seq_primer_clip/seq_primer_clip.xml
@@ -1,4 +1,4 @@
-<tool id="seq_primer_clip" name="Primer clip sequences" version="0.0.16">
+<tool id="seq_primer_clip" name="Primer clip sequences" version="0.0.18">
     <description>Trim off 5' or 3' primers</description>
     <requirements>
         <requirement type="package" version="1.0.1">galaxy_sequence_utils</requirement>
diff --git a/tools/seq_rename/README.rst b/tools/seq_rename/README.rst
index 765660f..d57d34e 100644
--- a/tools/seq_rename/README.rst
+++ b/tools/seq_rename/README.rst
@@ -1,7 +1,7 @@
 Galaxy tool to rename FASTA, QUAL, FASTQ or SFF sequences
 =========================================================
 
-This tool is copyright 2011-2017 by Peter Cock, The James Hutton Institute
+This tool is copyright 2011-2023 by Peter Cock, The James Hutton Institute
 (formerly SCRI, Scottish Crop Research Institute), UK. All rights reserved.
 See the licence text below.
 
@@ -85,6 +85,7 @@ v0.0.8  - Updated to point at Biopython 1.67 (latest version in Tool Shed).
 v0.0.9  - Use ``<command detect_errors="aggressive">`` (internal change only).
         - Single quote command line arguments (internal change only).
         - Python 3 compatible print function.
+v0.0.10 - Fix file open mode for Python 3.11 onwards.
 ======= ======================================================================
 
 
diff --git a/tools/seq_rename/seq_rename.py b/tools/seq_rename/seq_rename.py
index cb56302..4c66e64 100644
--- a/tools/seq_rename/seq_rename.py
+++ b/tools/seq_rename/seq_rename.py
@@ -17,7 +17,7 @@
 molecular biology and bioinformatics. Bioinformatics 25(11) 1422-3.
 https://doi.org/10.1093/bioinformatics/btp163 pmid:19304878.
 
-This script is copyright 2011-2017 by Peter Cock, The James Hutton Institute UK.
+This script is copyright 2011-2023 by Peter Cock, The James Hutton Institute UK.
 All rights reserved. See accompanying text file for licence details (MIT
 license).
 """
@@ -27,7 +27,7 @@
 import sys
 
 if "-v" in sys.argv or "--version" in sys.argv:
-    print("v0.0.9")
+    print("v0.0.10")
     sys.exit(0)
 
 # Parse Command Line
diff --git a/tools/seq_rename/seq_rename.xml b/tools/seq_rename/seq_rename.xml
index ff6f4e1..e444f9f 100644
--- a/tools/seq_rename/seq_rename.xml
+++ b/tools/seq_rename/seq_rename.xml
@@ -1,4 +1,4 @@
-<tool id="seq_rename" name="Rename sequences" version="0.0.9">
+<tool id="seq_rename" name="Rename sequences" version="0.0.10">
     <description>with ID mapping from a tabular file</description>
     <requirements>
         <requirement type="package" version="1.0.1">galaxy_sequence_utils</requirement>
diff --git a/tools/seq_select_by_id/README.rst b/tools/seq_select_by_id/README.rst
index 909c0a4..1232e63 100644
--- a/tools/seq_select_by_id/README.rst
+++ b/tools/seq_select_by_id/README.rst
@@ -1,7 +1,7 @@
 Galaxy tool to select FASTA, QUAL, FASTQ or SFF sequences by ID
 ===============================================================
 
-This tool is copyright 2011-2017 by Peter Cock, The James Hutton Institute
+This tool is copyright 2011-2023 by Peter Cock, The James Hutton Institute
 (formerly SCRI, Scottish Crop Research Institute), UK. All rights reserved.
 See the licence text below.
 
@@ -91,6 +91,7 @@ v0.0.12 - Python style changes (internal change only).
         - Python 3 compatible print function.
 v0.0.13 - Python 3 compatible exception handling.
 v0.0.14 - Script works on Python 2 and 3 (fixed output file mode).
+v0.0.15 - Fixed file open mode for Python 3.11 onwards.
 ======= ======================================================================
 
 
diff --git a/tools/seq_select_by_id/seq_select_by_id.py b/tools/seq_select_by_id/seq_select_by_id.py
index bcaeb11..8f0950b 100755
--- a/tools/seq_select_by_id/seq_select_by_id.py
+++ b/tools/seq_select_by_id/seq_select_by_id.py
@@ -16,7 +16,7 @@
 molecular biology and bioinformatics. Bioinformatics 25(11) 1422-3.
 https://doi.org/10.1093/bioinformatics/btp163 pmid:19304878.
 
-This script is copyright 2011-2017 by Peter Cock, The James Hutton Institute UK.
+This script is copyright 2011-2023 by Peter Cock, The James Hutton Institute UK.
 All rights reserved. See accompanying text file for licence details (MIT
 license).
 """
@@ -26,7 +26,7 @@
 import sys
 
 if "-v" in sys.argv or "--version" in sys.argv:
-    print("v0.0.14")
+    print("v0.0.15")
     sys.exit(0)
 
 # Parse Command Line
diff --git a/tools/seq_select_by_id/seq_select_by_id.xml b/tools/seq_select_by_id/seq_select_by_id.xml
index e38d068..d0a201d 100644
--- a/tools/seq_select_by_id/seq_select_by_id.xml
+++ b/tools/seq_select_by_id/seq_select_by_id.xml
@@ -1,4 +1,4 @@
-<tool id="seq_select_by_id" name="Select sequences by ID" version="0.0.14">
+<tool id="seq_select_by_id" name="Select sequences by ID" version="0.0.15">
     <description>from a tabular file</description>
     <requirements>
         <requirement type="package" version="1.67">biopython</requirement>