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  • khb
    Member
    • Dec 2010
    • 15

    Long peaks

    Hi
    I've done a chip-seq experiment, and used the program MACS. When I look at the peaks in UCSC genome browser, the peaks are very long, see pdf file for example from mitochondrial chromosome. Is this peak likely too bee a real peak?
    We believe that it will not bind direct to a DNA but likely as a part of a complex.
    Thanks for all replies
    Attached Files
  • csoong
    Member
    • Jun 2009
    • 74

    #2
    Never had any chip-seq experience. But are the peaks directly related to coverage? since chip-seq only selects a portion of the genome having high coverage (hence seeing higher peaks) is expected, right?

    By the way, what were you expecting? And please forgive me if I totally misunderstood your question.

    Comment

    • danielr
      Member
      • Sep 2009
      • 11

      #3
      If it's on the mitochondrial chromosome, assume it's not real. You pick up things there because it doesn't have the same copy number as the nuclear chromosomes.

      Comment

      • epigen
        Senior Member
        • May 2010
        • 101

        #4
        The length of your peaks depends on the value for the --bw parameter you give MACS. It should be the same as the fragment size. The higher the value, the longer the peaks.

        Comment

        • mudshark
          Senior Member
          • Jan 2009
          • 138

          #5
          looks weird.

          what was your experimental layout, did you use a control/input sample?

          is your chip target supposed to enter the mitochondria, is it a mitochondrial protein, is your result plausible?

          did you try any other peak caller, SISSR, Quest?

          Comment

          • mapper
            Member
            • Nov 2010
            • 17

            #6
            I have also seen very large peaks with MACS ...you can either use peak splitter program...or you can try sissr which will give very sharp peaks....

            Comment

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