Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • tahamasoodi
    Success
    • May 2012
    • 130

    Calculating sequence coverage

    How can we calculate the coverage of Illumina paired end whole genome sequencing data using Waterman equation? Example data is given:

    Total reads = 450,000,000
    Read length = 101
    Genome size = 3000000000
    Thanks,
  • lorendarith

    #2


    The Lander/Waterman equation is a method for computing coverage.
    The general equation is:

    C = LN / G

    • C stands for coverage
    • G is the haploid genome length
    • L is the read length
    • N is the number of reads

    So, if we take one lane of single read human sequence with v3 chemistry, we get

    C = (100 bp)*(189×10^6)/(3×10^9 bp) = 6.3

    This tells us that each base in the genome will be sequenced between six and seven times on average.

    ---------------------

    Though take care whether the "total reads" number is really the number of all reads (read 1 + read 2) or actually the "total pair" number. In the first case, you can just do the equation, however if it's the latter then you need to

    C = 2*LN/G
    Last edited by Guest; 12-08-2012, 10:03 AM.

    Comment

    • tahamasoodi
      Success
      • May 2012
      • 130

      #3
      How can we know whether it is total number or paired number?
      Thanks,

      Comment

      Latest Articles

      Collapse

      • 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
      • SEQadmin2
        From Collection to Sequencing: Why Sample Preparation and Preservation Define Sequencing Data
        by SEQadmin2


        Data variability is still an issue in sequencing technologies despite the advances in reproducibility and accuracy of these platforms. But the problem does not originate in the sequencing itself, but in the previous steps, before the sample reaches the sequencer.


        The first step is collection, followed by preservation and sample preparation for analysis. Most scientists overlook those steps, but not being careful might just be skewing the experiment’s results.
        ...
        06-02-2026, 10:05 AM

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by SEQadmin2, 06-17-2026, 06:09 AM
      0 responses
      24 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 06-09-2026, 11:58 AM
      0 responses
      42 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 06-05-2026, 10:09 AM
      0 responses
      48 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 06-04-2026, 08:59 AM
      0 responses
      49 views
      0 reactions
      Last Post SEQadmin2  
      Working...