Thanks Airan,
I am working with Arabidopsis.. so what I did, grow plants on different plates and then pooled them before sending for RNAseq.
I want to see if the ncRNA (smallRNAseq) are somehow related to their targets in transcriptome (longRNAseq)?.
Here is the complication with my data (if I still decide to ahead with analysis).
- m1 at 16C
- m2 at 16C
- m1m2 at 16C
- WT at 16C
- m1 at 23C
- m2 at 23C
- m1m2 at 23C
- WT at 23C
What kind of magic will help me get the best out of this.. You can understand that I already spent a lot on doing the two types of RNAseq on all these samples (doing them in triplicate would have bankrupted me).
I have the cuffdiff out put from cufflinks.. and am trying my luck with R and cummeRbund.. is there a way out in cummeRbund.. (please note I am the beginning in R)..