Hi, I'm new to Galaxy and am trying to view several miRNA datasets as a
differential expression. The pipeline I'm using is Bowtie for Illumina
(paired-end run) > SAM-to-BAM > ? > xls. The references I used with Bowtie
are a mature miRNA fasta and a piRNA fasta and the reads are 30nt in length.
So, my questions are: Is this the proper pipeline? How do I go about
converting the BAM into a xls file viewable in Excel?
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: