Here’s a random question. If some bacterial RNA-SEQ data was assembled with Trinity, the same RNA-SEQ data can be aligned with the obtained transcriptome assembly and read the expression level?
I mean as a concept, not what tools I can use.
Thanks!
Here’s a random question. If some bacterial RNA-SEQ data was assembled with Trinity, the same RNA-SEQ data can be aligned with the obtained transcriptome assembly and read the expression level?
I mean as a concept, not what tools I can use.
Thanks!
Hi @Sammy,
sure, it has sense. Indeed there is an under-development training in Galaxy on this approach.
Regards