Hi,

Two things:
- I've just installed BASE 2.11 and I'm trying without success to import 
CEL files in batch mode using the core plugin "Raw bioassay Importer". 
Even with a single file in the text file given in the configuration it 
doesn't work completly.
-> I uploaded the cdf and imported the reporters
-> I uploaded the CEL files and put them directly in the /home directory
-> I'm giving a file containing a single line and the following columns: 
Name, Array Design, Platform, File:

Name    Array Design    File    Platform
GSM30082    Mouse430A_2    /home/GSM30082.CEL    Affymetrix

The CEL file is taken from the GEO database at:
http://www.ncbi.nlm.nih.gov/projects/geo/query/acc.cgi?acc=GSM30082

I run the plugin as root. The plugin runs properly without any error 
(even in dry mode with all errors turned on leading to failure) but the 
CEL file is not attached to the Bioassay. When I create a single 
Bioassay with the same CEL file using the "New" button in the Bioassay 
list everything is fine, the CEL file is attached and the metadata is 
imported.
Any idea about that? Am I doing something wrong?

- Another more general thing: I would need to setup a production server 
for a microarray facility for them to test the BASE capabilities, and 
I'd really really want they go for it, instead of going for an expensive 
commercial solution. I would like to see some recommended guidelines or 
tutorials on that matter, as the system allows to do a lot of stuff, but 
I'm sure there is a best way to do it.
As I said I'm very supportive of the BASE project but I find it hard to 
get stuff completely automated in a simple way.
Indeed I find it very complex to set it up ready for use with all the 
platforms pre-installed so that the users can just pick and choose their 
array designs (at least for the standard ones: Affy, Illumina): one 
needs to import the array-design, then the reporters, then when 
importing Raw bioassay the users need to create a file for each import 
where information is redundant on each line (Platform, Array Design, 
etc...), whereas only the CEL file's name and eventually the Bioassay's 
name looks relevant to me.
Another thing is that I find it difficult not to be lost and confused 
with the reporter list view because the reporter's name is not forced to 
be unique, and the useful reporter list item is not used in an automatic 
way to make meaningful groups of reporters. For example is there a way 
to quickly access the reporters used in an array-design? How do you find 
your way amongst thousands of probe names and how to be sure we are not 
misusing reporters that have the same names (coming from automatic 
import from CDF or GAL files) but are biologically different?

Thank you for your help,
Renaud

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