| 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) |
_______________________________________________ Artemis-users mailing list [email protected] http://lists.sanger.ac.uk/mailman/listinfo/artemis-users
