Seqanswers Leaderboard Ad

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • 454 quality score, z-score,..

    Hey!
    I read something about 454 sequencing, but there are some things I don't understand. (http://www.nature.com/nature/journal...ture03959.html)

    Quality Score: Why is the quality score the probability, that a homopolymer of at least length n caused the signal, not exactly length n? And in the formula, the j-variable of the sum-symbol goes from n to infinity?

    Z-Score: If we need a reference sequence to calculate the Z-Score, we can only use it when resequencing a genome, not when we are doing a de novo assembly. In the supplementary methods it says it is also applicalbe when doing the de novo sequencing, but how? Just align the reads? And what is aligned, the peaks of the flowgrams?
    Furthermore, if the Z-Score is the difference between the averaged signal values of the different reads and the nearest integer, divided by the standard deviation of the read signals, wouldn't an averaged signal of e.g. 6.5 give rise to a higher Z-Score than an averaged signal of 6.9 when having the same standard deviation?? Or do I misinterpret the meaning of the Z-Score (confidence, that there is one particular base at a particular position)?

    Flow order: There appear two PPi Kernels during sequencing. Are they used to measure the amount of enzyme-beads and fragments (to correct the signal strength for each well)?

    Thanks,
    david

  • #2
    454 quality score

    Hi,

    as far as I can tell, there must be an error in the quality score definition...

    In the link you provide above (http://www.nature.com/nature/journal...ture03959.html), Margulies et al. (2005) states that the quality score is:
    Q = -10 log10( P(≥n|s) )
    where s is the observed signal and n is the length of the homopolymer that produced the signal.

    That would mean that:
    Q = 40 <=> P(≥n|s) = 0.0001
    Q = 20 <=> P(≥n|s) = 0.01

    So the probability that the homopolymer is of length ≥n is higher when the quality score is lower! That must be a mistake.

    How should one interpret the quality scores?

    Margulies (2005) writes:
    "For instance, if two A’s are called for a particular signal, the quality score for the second A is given by the probability that the observed signal came from a homopolymer of length two or greater."
    Here is some real 454 data:
    Code:
    Position: 1  2  3  4  5  6  7  8  9  10 11
    Residue:  T  G  G  G  A  G  G  G  G  A  T 
    Quality:  30 27 30 30 28 14 14 13 13 19 20
    So in the data above, what does it mean (in terms of probabilities), that:
    a) position 2 has lower quality than the rest of the homopolymer?
    b) position 7 has higher quality than the rest of the homopolymer?

    Anybody know how the quality score is calculated (eg. sourcecode)?

    Cheers,
    T
    Last edited by TSR; 08-30-2011, 04:05 AM.

    Comment


    • #3
      454 quality score, no error

      Their formula and coding are fine.
      Reported is the probability to their ERROR Model.

      Comment

      Latest Articles

      Collapse

      • seqadmin
        Essential Discoveries and Tools in Epitranscriptomics
        by seqadmin


        The field of epigenetics has traditionally concentrated more on DNA and how changes like methylation and phosphorylation of histones impact gene expression and regulation. However, our increased understanding of RNA modifications and their importance in cellular processes has led to a rise in epitranscriptomics research. “Epitranscriptomics brings together the concepts of epigenetics and gene expression,” explained Adrien Leger, PhD, Principal Research Scientist on Modified Bases...
        Yesterday, 07:01 AM
      • seqadmin
        Current Approaches to Protein Sequencing
        by seqadmin


        Proteins are often described as the workhorses of the cell, and identifying their sequences is key to understanding their role in biological processes and disease. Currently, the most common technique used to determine protein sequences is mass spectrometry. While still a valuable tool, mass spectrometry faces several limitations and requires a highly experienced scientist familiar with the equipment to operate it. Additionally, other proteomic methods, like affinity assays, are constrained...
        04-04-2024, 04:25 PM

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by seqadmin, 04-11-2024, 12:08 PM
      0 responses
      39 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 04-10-2024, 10:19 PM
      0 responses
      41 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 04-10-2024, 09:21 AM
      0 responses
      35 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 04-04-2024, 09:00 AM
      0 responses
      55 views
      0 likes
      Last Post seqadmin  
      Working...
      X