I am trying to run STAR alignment for pair-end reads and keep getting this error: "EXITING: because of fatal INPUT file error: could not open read file: Read1. I can't find where is the problem in my syntax. Here is my code:
cd /cs/labs/michall/yaelh/Projects/dsRNA-seq
# Mapping to masked genome:
STAR --runThreadN 6  \
     --runMode alignReads \
     --readFilesCommand gunzip -c \
     --genomeDir /Star_indices/Nve_genome_masked_index \     
     --readFilesIn  /output_files/Trimmomatic_out_paired/ad1_IgG_S10_R1_001_Trimmo_out_paired.fastq.gz  \
                    /output_files/Trimmomatic_out_paired/ad1_IgG_S10_R3_001_Trimmo_out_paired.fastq.gz  \       
     --outFileNamePrefix /Star_results/ad1_IgG_S10_R1_ \
     --outSAMtype BAM SortedByCoordinate \
     --outSAMunmapped Within \
     --outSAMattributes Standard \
     --quantMode TrancriptomSam GeneCount
 
    