Hi Susan,

Sorry for the delay in response. Are you still experiencing these problems? If 
so, would you mind sharing a history and your workflow with me and I will take 
a look.


Thanks for using Galaxy,

Dan


On Sep 20, 2011, at 4:28 PM, Susan Newman wrote:

> I’m working on a SOLiD ChIP-Seq workflow in which I want to use SICER for 
> peak detection.  In attempting to add SICER to the workflow, I’ve run into 
> some difficulty:
>  
> 1)       My input is an interval file which I’ve created using Convert SAM.  
> In order to connect to the SICER module, I had to use a trick by setting up 
> the connection with the Convert SAM set to BED.  The SICER algorithm fails to 
> run when tested with the bed file.  If I then change the connected Convert 
> SAM to interval, SICER will run.
> 2)      I need to change the default run parameters but they are not saved in 
> the workflow.   There is always reversion to the default values. I get a 
> Server error notice.  This workflow also contains Bowtie and MACS.  Parameter 
> changes for these algorithms are saved correctly.
> 3)      I would like to run SICER twice in the workflow with different 
> parameters.  Is it allowable to load SICER a second time?  May I run from the 
> same interval conversion file?  I tried this and again could not get the 
> input file recognized as a valid connection.
> Thanks in advance,
>  
> Susan
>  
> Susan S. Newman, Laboratory Manager
> Genomics Core Facility, L2012
> Pennington Biomedical Research Center
> 6400 Perkins Road
> Baton Rouge, LA  70808
> 225-763-0255 (o) 225-763-0257 (lab)
>  
> http://gcf.pbrc.edu
>  
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