Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • chinamrwu
    Junior Member
    • May 2013
    • 1

    #1

    help for computing relative mCpG density

    Hi :
    Anybody can help me ?
    I am computing the relative DNA methylated Cytosine density of genome, and
    confused by the following question:
    the DNA sequence is AACGCTT and the methylation level of CGC are 0.6, 0.8,1.0 respectively. Now, is the retio of mCG values to total numbers of CGs
    is (0.6+0.8)/2=0.7 or (0.8+1.0)/2=0.9 or (0.6+0.8+1.0)/3=0.8 or [(0.6+0.8)/2+(0.8+1.0)/2]/2=0.8 ? which is correct among the four methods ?

    thanks
  • C.R.
    Member
    • Jun 2010
    • 25

    #2
    In my understanding it is like this: the sequence you provide contains one CpG site which can be sequence from forward and reverse strand. However, if you want to calculate the methylated cytosine density from all cytosines (and you do not restrict yourself to CpG sites) it will be more complex. On the other hand people usually discriminate between CpG, CHG and CHH.

    Comment

    Latest Articles

    Collapse

    • SEQadmin2
      Multiomic Liquid Biopsy: What DNA/RNA Panels Reveal That DNA Alone Can’t
      by SEQadmin2



      Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?

      Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating
      ...
      Today, 09:55 AM
    • SEQadmin2
      New Genomics Technologies Take Aim at Long-Standing Limits
      by SEQadmin2


      Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.

      We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing
      ...
      09-28-2026, 10:25 AM

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by SEQadmin2, Today, 05:39 AM
    0 responses
    10 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, Yesterday, 09:56 AM
    0 responses
    11 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 10-09-2026, 11:14 AM
    0 responses
    25 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 09-29-2026, 09:51 AM
    0 responses
    77 views
    0 reactions
    Last Post SEQadmin2  
    Working...