Entering edit mode
5.0 years ago
asumani
▴
70
Hi all,
I am working with 24nt siRNA. I downloaded sRNA data online, aligned my reads to miRNA.fa and extracted unaligned reads. Then I converted bam to fastq and I extracted only 24nt length reads.
For statistical analysis I want to have random 24mers as control data-set. Any suggestion for how to perform that?
Thanks, Asuman
It just helped perfectly indeed. Many thanks!