Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • bedward1
    Junior Member
    • Aug 2013
    • 2

    Non-C methylation in Bismark .cov files

    Hi
    I am analyzing RRBS using TrimGalore/Bismark and the methylation extractor, and am noticing quite a few non-C (T, A, and G) methylation signals (maybe 20% compared to C, by eye). Is this a normal technical artifact that has been observed?
    Thanks
    --Bryan
  • dpryan
    Devon Ryan
    • Jul 2011
    • 3478

    #2
    In the case of G, that is a C, just on the other strand. In the case of T or A, that's either an off by 1 error or the sequence you're looking at is different from the sequence against which the aligning was done.

    Comment

    • bedward1
      Junior Member
      • Aug 2013
      • 2

      #3
      Thanks for the replay Devon.
      Is the 'off by 1 error' common? What would cause this?
      --Bryan

      Comment

      • dpryan
        Devon Ryan
        • Jul 2011
        • 3478

        #4
        Off by 1 errors are quite common (common enough that it has its own wikipedia article). The likely cause is the file using 1-based coordinates while whatever you're using to visualize things assumes it's using 0-based coordinates. I remember this being an issue with some of bismark's output at one point, though I don't know what the status of that is. If you look at those and there's an appropriate C (or G, depending on how things were done) just to the right, then that's what's going on.

        Comment

        • fkrueger
          Senior Member
          • Sep 2009
          • 627

          #5
          Wouldn't off-by-1 errors more result in 50/50 values than 20%? I'd be happy to have a closer look at whatever problems you are running into, just drop me a line.

          Comment

          • dpryan
            Devon Ryan
            • Jul 2011
            • 3478

            #6
            Given the non-random distribution of bases in the genome, probably not.

            Comment

            Latest Articles

            Collapse

            • GATTACAT
              Reply to Nine Things a Sample Prep Scientist Thinks About Before Sequencing
              by GATTACAT
              Love this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
              07-01-2026, 11:43 AM
            • SEQadmin2
              Nine Things a Sample Prep Scientist Thinks About Before Sequencing
              by SEQadmin2


              I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.

              Here are nine questions we think about, in roughly the order they matter, before...
              06-18-2026, 07:11 AM

            ad_right_rmr

            Collapse

            News

            Collapse

            Topics Statistics Last Post
            Started by SEQadmin2, 07-02-2026, 11:08 AM
            0 responses
            12 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 06-30-2026, 05:37 AM
            0 responses
            14 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 06-26-2026, 11:10 AM
            0 responses
            20 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 06-17-2026, 06:09 AM
            0 responses
            54 views
            0 reactions
            Last Post SEQadmin2  
            Working...