This is not an Artemis question as much as it is a file manipulation program question....

I have an intensity profile from a whole genome tiling array.  The file consists of about 128,000 fluorescence  intensity measurements.  I know the genomic location of each intensity number and I want to use these intensities as a "User Plot".  Unfortunately, the genome has a total of 1.47 million bases and I need to add "padding" between the intensity numbers so that the graph lines up with the annotation. I would be totally satisfied with just replicating the adjacent numbers to fill in the gaps.

Does anyone have a suggestion as to ho to do this? Or is there another method entirely?

Mike

Michael J. Herron,  U of MN, Dept. of Entomology
     612-624-3688 (office) 612-625-5299 (FAX)



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