Dear All,
Thank you for this script and providing the support for the user.
I tried to make the first run but I noticed it does not support providing a folder as input for multiple file of fastq.gz. It required to make it one by one. I have 117 samples. Is there any way to automate this process?
Also, I am looking to way to count the reads number before doing any filteration for human reads and after remove these reads and after trimming. I hope this script can do this as this will help to nderstand where is the lost happen specially for trimming step.
Regards,
Faisal