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  • genbio64
    Member
    • Dec 2009
    • 42

    #1

    Igv

    Greetings All,
    I have been using IGV to view my bowtie alignments in BAM format but am experiencing some difficulty. I have to drill down to the last 2 levels of sequence magnification to actually see where my alignments match up against my reference. Does anyone else have this issue? Additionally, is there a away that I can format these so I do not have to drill down so far, thus allowing me to look at a more global picture of the RefSeq genes? any help is appreciated.

    Cheers,
    Genbio64
  • Thomas Doktor
    Senior Member
    • Apr 2009
    • 105

    #2
    You need to make a coverage profile using the "igvtools count" command, this will create a lightweight coverage profile which can be seen on a global scale.

    The command would be something like:
    igvtools count alignment.bam alignment.bam.tdf hg19

    Read more here: http://www.broadinstitute.org/igv/igvtools

    Comment

    • genbio64
      Member
      • Dec 2009
      • 42

      #3
      @Thomas Doktor,
      Thanks for the info but everytime I attempt to run the igvtools count command it tells me it cannot find the genome file, regardless if I give it the name "hg19" or the full path. any ideas?

      Comment

      • Jim Robinson
        Member
        • May 2009
        • 75

        #4
        Hi, if you're still having troubles with this email [email protected].

        You can increase the window size for which alignments are displayed from the user preferences, click "View > Preferences > Alignments (tab)" and change the "Visibility Range Threshold". Its set for 30kb, which is a reasonable default, but if your coverage is not excessively deep you can increase it safely.

        I don't know why you are getting the error with igvtools, again if you're still experiencing this please email.

        Jim

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