diff --git "a/src/RNAseq sen1\342\210\206.nf" "b/src/RNAseq sen1\342\210\206.nf"
index 8695b03e6fa8717b3462a68f9940f83ceef4c570..eda4e8a0afb8fcb5336f4acc2db0e1ec8adfe754 100644
--- "a/src/RNAseq sen1\342\210\206.nf"	
+++ "b/src/RNAseq sen1\342\210\206.nf"	
@@ -10,7 +10,7 @@
 * for paired-end data
 */
 
-params.fastq = "$baseDir/data/fastq/*_R{1,2}_001.fastq"
+params.fastq = "$baseDir/data/fastq/*_R{1,2}_001.fastq.gz"
 
 log.info "fastq files : ${params.fastq}"
 
@@ -27,11 +27,11 @@ process adaptor_removal {
   set pair_id, file(reads) from fastq_files
 
   output:
-  set pair_id, "*_cut_R{1,2}.fastq.gz" into fastq_files_cut
+  set pair_id, "*_cut_R{1,2}_001.fastq.gz" into fastq_files_cut
 
   script:
   """
-  cutadapt -a TGGAATTCTCGGGTGCCAAGG -g CCTTGGCACCCGAGAATTCCA -A TGGAATTCTCGGGTGCCAAGG -G CCTTGGCACCCGAGAATTCCA \
+  cutadapt -a TGGAATTCTCGGGTGCCAAGG -A GTTCAGAGTTCTACAGTCCGACGATC \
   -o ${pair_id}_cut_R1.fastq.gz -p ${pair_id}_cut_R2.fastq.gz \
   ${reads[0]} ${reads[1]} > ${pair_id}_report.txt
   """