Hi,
I have around 150 PE reads and because running PEAR on them singularly would be a pain, I am trying to run it through a batch.
I have 2 text files (R1.txt and R2.txt). The first text file lists the names of the all the forward reads and the second text file lists all the reverse reads (corresponding to the forwards reads).
When I run PEAR directly from the compiler, it recognizes the fastq files and merges it the usual way, but when i run it using a shell script, i get the same error "[ERROR] - Cannot open file XXXXXXX_R2.fastq".
I shall highly appreciate if anyone can help me with this.
Thanks & Regards
anaqib2