# HG changeset patch
# User galaxytrakr
# Date 1789473756 0
# Node ID ecf96ad086119d320116e6b2dc44260ec68bd3b8
# Parent  45ac0b1424fc25a9550ba51ff8e5746ccda0c710
planemo upload commit 26a6ad9e9ae7fdb967832a65f5173ea347da7f6c

diff -r 45ac0b1424fc -r ecf96ad08611 Dockerfile
--- a/Dockerfile	Mon Sep 14 20:27:08 2026 +0000
+++ b/Dockerfile	Tue Sep 15 12:02:36 2026 +0000
@@ -10,6 +10,7 @@
 
 WORKDIR /workspace
 
+
 # Build dependencies: compiler, zlib dev headers, git, Python
 RUN apt-get update && apt-get install -y --no-install-recommends \
     build-essential \
diff -r 45ac0b1424fc -r ecf96ad08611 mitokmer.xml
--- a/mitokmer.xml	Mon Sep 14 20:27:08 2026 +0000
+++ b/mitokmer.xml	Tue Sep 15 12:02:36 2026 +0000
@@ -1,7 +1,7 @@
-<tool id="mitokmer" name="mitoKmer" version="2.0+galaxy0.1" python_template_version="3.5" profile="21.05">
+<tool id="mitokmer" name="mitoKmer" version="2.0+galaxy0.2" python_template_version="3.5" profile="21.05">
     <description>Identify metagenomic mitochondrial reads by k-mer database matching</description>
     <requirements>
-        <container type="docker">quay.io/galaxytrakr/mitokmer:927c4ee</container>
+        <container type="docker">quay.io/galaxytrakr/mitokmer:e57a559</container>
     </requirements>
 
     <command detect_errors="exit_code"><![CDATA[
@@ -13,8 +13,8 @@
         mkdir -p ./mitochondria7 ./jobs7m &&
 
         ## ── Link database files from the data table directory ─────────────────
-        ## The data table path points to a directory containing all the
-        ## mitochondria7 .txt files; symlink each one into ./mitochondria7/
+        ## Symlink each file individually from the registered database directory.
+        ## Note: glob must be outside quotes so the shell expands it correctly.
         ln -sf '${probe_db.fields.path}'/* ./mitochondria7/ &&
 
         ## ── Symlink kmerread7 into the working directory ──────────────────────
@@ -23,13 +23,15 @@
         ln -sf /usr/local/bin/kmerread7 ./kmerread7 &&
 
         ## ── Write the jobs file ───────────────────────────────────────────────
-        ## Format: sample_name  num_files
+        ## Format: sample_name <tab> num_files
         ##         /abs/path/to/read1
         ##         /abs/path/to/read2  ...
-        #set sample_name = $reads[0].element_identifier.replace(' ', '_').split('_')[:-1] | join('_')
-        printf '${sample_name}\t${reads|length}\n' > ./jobs7m/jobs7m.txt &&
+        ## Use len() to safely get collection size as an integer
+        #set sample_name = $reads.name.replace(' ', '_')
+        #set read_count = len($reads)
+        printf '%s\t%d\n' '${sample_name}' ${read_count} > ./jobs7m/jobs7m.txt &&
         #for read in $reads
-            printf '${read.file_name}\n' >> ./jobs7m/jobs7m.txt &&
+            printf '%s\n' '${read.file_name}' >> ./jobs7m/jobs7m.txt &&
         #end for
 
         ## ── Run the Python orchestrator (no arguments) ────────────────────────
@@ -58,7 +60,6 @@
             </options>
         </param>
 
-        <!-- One or more FASTQ/FASTA files for a single sample -->
         <param name="reads"
                type="data_collection"
                collection_type="list"