Question: Combining The Paired Reads From Illumina Run
0
Surya Saha • 80 wrote:
Hi,
I have two fastq files with the forward(/1) and reverse(/2) paired
reads.
The reads are not in same order in either file, some pairs are
absent/missing and the files are 8 GB each with abt 30 mill reads
each.
I am trying to pull out all the paired reads for which both fwd and
rev
exist. Can I use a combination of fastq tools in Galaxy to do this?
Thanks!
-Surya
ADD COMMENT
• link
•
modified 7.7 years ago
by
Florent Angly • 370
•
written
7.7 years ago by
Surya Saha • 80