I have RNA seq datasets from which i aim create a Transcriptome Assembly. The datasets which I have are from different sources some from Illumina and some from 454. I have been able to create an assembly with about 10 datasets from 454. The process went smooth and good. I now have to concatenate datasets which has been run on Illumina. I want help in regards on how to go ahead with merging the two datasets using galaxy.
Looking forward to your reply.