Hi!

We are interested in running a GISTIC analysis on the data we obtained
after segmentation with GLAD with Aroma, but there seems to be a
problem regarding the start and end postions of the segments, which
apparently do not match the physical positions of the markers file we
are using for GISTIC.

Does the segmentation reports the actual physical position of the
first and last markers or does it reports other nearby position?

Another question, I have a copy number file obtained from paired
analyisis in Partek Genomics Suite, and want to do the segmentation
using GLAD or CBS. How can I incorporate my CN file into the Aroma
pipeline to do the segmentation?

Thanks al lot!!

-- 
When reporting problems on aroma.affymetrix, make sure 1) to run the latest 
version of the package, 2) to report the output of sessionInfo() and 
traceback(), and 3) to post a complete code example.


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