Hello. I am trying to count miRNAs using exceRpt pipeline (using Genbree, not Docker because it dosen't work). I could count miRNA expressions in single-read …
my paired end rna seq data includes solexa library preparation, and illumina hiseq 2000... can't understand by any means that whether to use `fr-unstranded`or `fr-firststrand`or …
Does anyone know how to get the average insert size of paired-end RNA seq data (excluding linkers and adapters)? These are Illumina Hiseq2000 data with …
Which library design (single end or paired end, short or long read length) would you choose for the detection of alternative splicing and fusion genes …
Hello poonam.bi01!
We believe that this post does not fit the main topic of this site.
Similar questions have been answered before. See links posted by @venu
For this reason we have closed your question. This allows us to keep the site focused on the topics that the community can help with.
If you disagree please tell us why in a reply below, we'll be happy to talk about it.
Cheers!