basecall_fast5_gpu.out.sequencing_summary à la place de ss pour le CQ bam

src/bolero.nf

@@ -275,15 +275,7 @@ workflow {
 
   hbv_genome(cut_5pRACE.out.fastq_cutadapt, genome.collect())
   sort_index_bam(hbv_genome.out.bam)
-  control_bam(ss.collect(), sort_index_bam.out.indexed_bam)
-
-  sort_index_bam.out.indexed_bam
-    .flatten()
-    .filter(~/.*bam$/)
-    .collect()
-    .set{bam_path}
-
-  //control_bam(ss, bam_path)
+  control_bam(basecall_fast5_gpu.out.sequencing_summary.collect(), sort_index_bam.out.indexed_bam)
 
   //###################### START POSITIONS #######################