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  • sindrle
    Senior Member
    • Aug 2013
    • 266

    Making nice image of chr1 coverage track in IGV

    Can anyone help me make this kind of image?

    I have calculated the coverage track and visualised (as log values) compared to chr1 in IGV.

    However in IGV i can't see the centromere, nor the whole chromosome, so the image is not as nice as this one...


    Click image for larger version

Name:	Screen Shot 2014-03-04 at 16.20.35.jpg
Views:	1
Size:	65.0 KB
ID:	308396
  • dpryan
    Devon Ryan
    • Jul 2011
    • 3478

    #2
    Have a look at the Gviz bioconductor package, it can create images like that.

    Comment

    • sindrle
      Senior Member
      • Aug 2013
      • 266

      #3
      Looks nice! I guess I just have to start trying.

      Thanks!

      Comment

      • sindrle
        Senior Member
        • Aug 2013
        • 266

        #4
        Just realised mouse don't have centromeres..

        Any good ideas how to make a similar image for mouse? Thanks!

        Comment

        • frozenlyse
          Senior Member
          • Sep 2008
          • 135

          #5
          That just looks like custom data loaded to UCSC?

          Comment

          • emp
            Member
            • Jan 2014
            • 11

            #6
            Hello,
            I want to visualise my mapped SAM file, as to how much of its part contains centromeric region.

            Kindly help me as to what tool should be used.

            Waiting for help...

            Comment

            • frozenlyse
              Senior Member
              • Sep 2008
              • 135

              #7
              Originally posted by emp View Post
              Hello,
              I want to visualise my mapped SAM file, as to how much of its part contains centromeric region.

              Kindly help me as to what tool should be used.

              Waiting for help...
              convert your sam to bam and then index using samtools, load into IGV

              Comment

              • sindrle
                Senior Member
                • Aug 2013
                • 266

                #8
                This what I did:

                used Igvtools count on every BAM in the experiment (took 2 days to calculate).

                Imported thes TDF into IGV along with correct genome.

                Saved chr1 as vector picture.

                Opened in Photoshop and moved the coverage track above the chromosome.

                Looks nice!

                Comment

                • dpryan
                  Devon Ryan
                  • Jul 2011
                  • 3478

                  #9
                  Never discount the utility of Photoshop/Illustrator when making figures

                  Comment

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