Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • dphansti
    Member
    • May 2011
    • 28

    #1

    quality scores discrepancy on wikipedia

    I am modifying code that automatically guesses the scoring method used in a fastq file. I am using the wikipedia entry for guidance (http://en.wikipedia.org/wiki/FASTQ_format).

    But the example they show has some discrepancies. In the top part of the image illumina-1.5+ scores start at position 66. But at the bottom of the image it starts at they start at 67.

    The bigger problem I am having is that some fastqs that I am looking at have quality scores of 'i' which is not consistent with any of the scoring methods listed on wikipedia.

    Can anyone clear this up for me? Is there a better source than wikipedia for this information?

    Thanks.
    Last edited by dphansti; 04-18-2013, 05:12 PM.
    Doug
    www.sharedproteomics.com
  • swbarnes2
    Senior Member
    • May 2008
    • 910

    #2
    Read the note in the wiki. B doesn't really mean 2, it means crappier than 2, or it means the end of the read is poor.

    Starting in Illumina 1.5 and before Illumina 1.8, the Phred scores 0 to 2 have a slightly different meaning. The values 0 and 1 are no longer used and the value 2, encoded by ASCII 66 "B", is used also at the end of reads as a Read Segment Quality Control Indicator.[6] The Illumina manual[7] (page 30) states the following: If a read ends with a segment of mostly low quality (Q15 or below), then all of the quality values in the segment are replaced with a value of 2 (encoded as the letter B in Illumina's text-based encoding of quality scores)... This Q2 indicator does not predict a specific error rate, but rather indicates that a specific final portion of the read should not be used in further analyses. Also, the quality score encoded as "B" letter may occur internally within reads at least as late as pipeline version 1.6
    So C, or 3, is the lowest true quality value you can get in that encoding system.

    If you have an "i", maybe you have a new read generated with new improved chemistry, which some quality scores of 41, that have for some reason been converted to the old quality scoring.

    Comment

    • maasha
      Senior Member
      • Apr 2009
      • 153

      #3
      In fact, Solexa and Illumina scores cover the whole of the printable ASCII alphabet (0-93) like Phred. However, mostly the scores are from 0-40, but with the new instruments you will often find scores above 40. If you read the wiki entry carefully it actually says so. Guessing correct encoding is a pest.

      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
        ...
        10-14-2026, 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, 10-22-2026, 11:13 AM
      0 responses
      23 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-22-2026, 10:48 AM
      0 responses
      20 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-15-2026, 10:52 AM
      0 responses
      36 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-14-2026, 05:39 AM
      0 responses
      42 views
      0 reactions
      Last Post SEQadmin2  
      Working...