Entering edit mode
6.0 years ago
Sillpositive
▴
20
Hello everybody. right now I'm trying to assemble the fast q files with reverse and forward read with the SortMeRNA script and then filter (r RNA). but however, I have a lot of files. I would like to know it is possible to launch a script that takes my first script (merge-paired-reads.sh) and does the work on all on all my files.
how does work merge-paired-reads.sh
:
bash scripts/merge-paired-reads.sh file_R1.fastq file_R2.fastq combined.fastq.
I have lot of files like this (54 to be precise):
example :
SRR3571052_1.fastq
SRR3571064_1.fastq
SRR3571072_1.fastq
SRR3571148_1.fastq
SRR3571158_1.fastq
SRR3571167_1.fastq
SRR3571179_1.fastq
SRR3571052_2.fastq
Thank you so much Pierre ( Merci beaucoup ) !
Another Question , it possible to delete old files ( ${F}_1.fastq ${F}_2.fastq ${F} ) to save hard drive space at the same time ?
Encore Merci !
it's a very basic bash question , consider this as an exercise.
Thank you so much again but i don't know, how and where i can put this condition rm -f ${F}_1.fastq* {F}_2.fastq* ?
Never delete original data files unless you have a backup. You will regret doing that later, if something goes wrong and you need to start over.
Thank you for response but I have a backup and no more space so I need to know how delete forward and reverse at the same time.
Hi, could you please share the dummy code which I can relate to, for the whole workflow (uncompressing, merging,sortMeRNA, unmerging). as I am a newbie for programming. I have the same problem. Thanks in advance.