Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • zeam
    Member
    • Oct 2010
    • 43

    Questions on the updated illumina quality score

    The quality of my datum from an updated illumina system is sanger/illumina 1.9 which confused me very much.Could I just treated them as sanger format?
    Can somebody familiar with this can give me some details about this kind of encoding pattern?
  • BAMseek
    Senior Member
    • Apr 2011
    • 124

    #2
    Hi zeam,

    I would suggest looking at the changes made to CASAVA 1.8 - there is a nice post about it here.

    I know they have switched the quality encodings from Phred+64 to the more standard Sanger encoding (ASCII = Phred+33) starting in CASAVA 1.8.

    Justin

    Comment

    • Robby
      Member
      • Mar 2011
      • 68

      #3
      @zeam: The new Illumina quality scores are in Sanger format and encode a Phred quality score from 0 to 93 using ASCII 33 to 126.

      But we are confused with the new quality scores as well. We use BWA for mapping. BWA has the extra option -I for quality scores in the Illumina 1.3+ read format (quality equals ASCII-64). I assume, that without that option BWA expect the old Illumina format. Is that correct? How do we have do use BWA correctly with the new Sanger format?

      Thanks Robby

      Comment

      • GenoMax
        Senior Member
        • Feb 2008
        • 7142

        #4
        Originally posted by zeam View Post
        The quality of my datum from an updated illumina system is sanger/illumina 1.9 which confused me very much.Could I just treated them as sanger format?
        Can somebody familiar with this can give me some details about this kind of encoding pattern?
        I assume you are referring to pipeline v.1.8 (I am sure there is a v. 1.9 somewhere in illumina labs in alpha/beta testing).
        If that is correct then your quality values will be in sanger format. You will also discover that if your facility uses v.3 chemistry then the valid range of quality values has been expanded beyond the previous max value of 40. You will see quality values of 41 (and up at some point in time), which are now possible.

        Comment

        • fpepin
          Member
          • Feb 2011
          • 30

          #5
          Originally posted by Robby View Post
          But we are confused with the new quality scores as well. We use BWA for mapping. BWA has the extra option -I for quality scores in the Illumina 1.3+ read format (quality equals ASCII-64). I assume, that without that option BWA expect the old Illumina format. Is that correct? How do we have do use BWA correctly with the new Sanger format?
          Not quite. They haven't updated the BWA documentation to say that that 1.3+ should be 1.3-1.7. With 1.8, just don't use the -I and you'll be doing just fine.

          Comment

          • maricu
            Junior Member
            • Apr 2010
            • 8

            #6
            Hi all,

            I noticed that BWA assigns mapping quality of 0 when it finds a "J" (or at least a bunch of them) in the quality string. So far I've opted for changing al J to I and then map with the default BWA so it assumes is sanger. I think a patch will be needed to correct this bug.

            Let me know if you have observed this as well.

            Comment

            • thk2008
              Junior Member
              • Oct 2011
              • 1

              #7
              Originally posted by GenoMax View Post
              I assume you are referring to pipeline v.1.8 (I am sure there is a v. 1.9 somewhere in illumina labs in alpha/beta testing).
              If that is correct then your quality values will be in sanger format. You will also discover that if your facility uses v.3 chemistry then the valid range of quality values has been expanded beyond the previous max value of 40. You will see quality values of 41 (and up at some point in time), which are now possible.
              Hi,

              Are the scores on a different scale or are there just more of them? I want to filter scores with a cutoff of 20. Previously, with the Phred+64 scores I would test with ASCII-64 > 20. So, can I do this with the Phred+33 scores, such as, ASCII-33 > 20?

              Thanks,
              Thadeous

              Comment

              Latest Articles

              Collapse

              • SEQadmin2
                Advanced Sequencing Platforms Tackle Neuroscience’s Toughest Genomics Problems
                by SEQadmin2



                Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
                ...
                07-09-2026, 11:10 AM
              • SEQadmin2
                Cancer Drug Resistance: The Lingering Barrier to Rising Survival
                by SEQadmin2



                Cancer survival rates have significantly increased in the last few decades in the United States, reaching a combined 70% 5-year survival rate by 2021. Behind this number, there are years of research to find new therapies, drug targets, and early detection methods. But there is one core challenge that keeps slowing down these advances, and it’s about drug resistance.

                There is no single reason why many patients don’t respond to treatment as expected. Cancer is...
                07-08-2026, 05:17 AM
              • 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

              ad_right_rmr

              Collapse

              News

              Collapse

              Topics Statistics Last Post
              Started by SEQadmin2, 07-13-2026, 10:26 AM
              0 responses
              20 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 07-09-2026, 10:04 AM
              0 responses
              30 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 07-08-2026, 10:08 AM
              0 responses
              17 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 07-07-2026, 11:05 AM
              0 responses
              34 views
              0 reactions
              Last Post SEQadmin2  
              Working...