Thanks.
Sent from Samsung mobile
Luciano Cosme cosme.sim...@gmail.com wrote:
Hi,
I believe you have to run Fastq Groomer first to convert it to sanger format.
Then you will be able to see your dataset.
https://main.g2.bx.psu.edu/u/dan/p/fastq
Best,
Luciano
DISCLAIMER
==
This e-mail may contain privileged and confidential information which is the
property of Persistent Systems Ltd. It is intended only for the use of the
individual or entity to which it is addressed. If you are not the intended
recipient, you are not authorized to read, retain, copy, print, distribute or
use this message. If you have received this communication in error, please
notify the sender and delete all copies of this message. Persistent Systems
Ltd. does not accept any liability for virus infected mails.
___
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:
http://lists.bx.psu.edu/listinfo/galaxy-dev
To manage your subscriptions to this and other Galaxy lists,
please use the interface at:
http://lists.bx.psu.edu/