It appear that you are talking about RNA-seq data analysis. If so please read a tutorial posted by Jeremy to get an idea how the work flow has to be used. I am sure folks would also like to know what error you are getting. --- On Thu, 7/28/11, archana bhardwaj <archana2287@gmail.com> wrote: From: archana bhardwaj <archana2287@gmail.com> Subject: [galaxy-user] query To: galaxy-user@lists.bx.psu.edu Date: Thursday, July 28, 2011, 4:23 AM Respected sir I am using fastaq to convert fasta and quality file. But after sometime i am getting an error and m not able to fix it. please guide me what sholud i do?? -----Inline Attachment Follows----- ___________________________________________________________ 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/