Hello mates,

I have two doubts galaxy:

a) I have rna-seq data from Illumina and do fastqc ... the results are good but 
when I fastgroomer to Sanger format and then fastqc ... the results are bad. 
Does anyone know the cause? I do not understand why.

b) With the same sequences can know if they are different Rna and eliminate 
those that do not want to examine?

merry christmas :)                                        
The Galaxy User list should be used for the discussion of
Galaxy analysis and other features on the public server
at usegalaxy.org.  Please keep all replies on the list by
using "reply all" in your mail client.  For discussion of
local Galaxy instances and the Galaxy source code, please
use the Galaxy Development list:


To manage your subscriptions to this and other Galaxy lists,
please use the interface at:


To search Galaxy mailing lists use the unified search at:


Reply via email to