diff --git a/test/output.md5 b/test/output.md5
index d4f428c..bd21798 100644
--- a/test/output.md5
+++ b/test/output.md5
@@ -21,5 +21,5 @@ eaa8bb5f32aa0ef05bcf923d0c2bd711  output/test_lca_taxa.uglyprint.mismatch
 70363c8585d69e8d4457fc1d1ba7cd92  output/test_lca.uglyprint.mismatch
 1f9c4d0ab804d6a6e077573e6c8e736a  output/test_lca.uglyprint.stat
 dc5bf1edd27b494e23f72d41d718600d  data/f570b1db7c.dedup.filtered.bam
-3568c671c0fa09797284746bb0528ddd  data/f570b1db7c.dedup.filtered.rname.bam
+c73c56f8a3e2dc9b13c949ec1404bd50  data/f570b1db7c.dedup.filtered.rname.bam
 #3568c671c0fa09797284746bb0528ddd  data/f570b1db7c.dedup.filtered.rname.bam ##apparantly samtools 1.20 has changed the within qname order when sorting by readname. This is of cause fine but some seqs would be reverse complemented. When switching to the new order then this entry should be used instead of the above