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  • canis
    Junior Member
    • Sep 2008
    • 3

    #1

    Minimum Coverage for ChIP-Seq & RNA-Seq

    Hi all,

    Can anyone please suggest what should be the minimum Coverage and Read Depth required to get meaningful results for ChIP-Seq and RNA-Seq analyses.

    Thanks,
    Veer
  • SGPSling
    Junior Member
    • Jun 2009
    • 8

    #2
    I don't think this question has been examined carefully to date. You may want to read the recent paper of Rozowsky et al. Nat. Biotech 27 (1) 66-75. The bottom line is different transcription factor has different saturation depth. We simply need ChIP seq data of more transcription factor to see if there is a generalized pattern for different class of TFs.

    Anyone can add more reference discussed the same matter will be really appreciated.

    Comment

    • canis
      Junior Member
      • Sep 2008
      • 3

      #3
      Thanks SGPSling I will go through the paper Rozowsky et al. Nat. Biotech 27 (1) 66-75. My understanding of what you have posted is that the saturation depth can not be predicted in advance , it will depend on the sample used. Am I correct in my understanding?

      Comment

      • james hadfield
        Moderator
        Cambridge, UK
        Community Forum
        • Feb 2008
        • 224

        #4
        SGPSling is correct but I would say 1 lane for ChIP-Seq and 2-3 for mRNA-Seq are good ballparks.

        Comment

        • SGPSling
          Junior Member
          • Jun 2009
          • 8

          #5
          Hi, Canis: I would say the saturation depth depends on the TF you are studying. In the paper I quoted, the identified peaks saturated arount 3-4 M reads for PolII so that one lane would be enough. But for STAT1, it didn't reach plateau even when they sequenced 24 M reads.

          For most of the ChIP seq papers published so far, they usually got 1-2 M reads. So James is right that people usually do one lane for each sample in a ChIP seq experiment at this moment.

          As for now, we cannot predict the saturation depth for ChIP. But I believe with more results published in the future, one migth be able to do so. At this stage, we simply need more data to improve our knowledge.

          Comment

          • SGPSling
            Junior Member
            • Jun 2009
            • 8

            #6
            Sorry, don't know where the thumbs down icon come from in my last post. It is not what I want.

            Comment

            • ECO
              --Site Admin--
              • Oct 2007
              • 1360

              #7
              Originally posted by SGPSling View Post
              Sorry, don't know where the thumbs down icon come from in my last post. It is not what I want.
              Fixed!

              Comment

              • james hadfield
                Moderator
                Cambridge, UK
                Community Forum
                • Feb 2008
                • 224

                #8
                I said one lanes should do for ChIP-Seq and that comment is based on us geting up to 20M reads from a single lane. We routinely get over 10M reads and (I am a little gobsmacked by this) saw a sinlge control lane generate 0.97Gbp from a 42 cycle run!
                If you only get 1-2M reads then you need more lanes!
                James.

                Comment

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