Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • vedbar
    Junior Member
    • May 2011
    • 5

    #1

    Fastx Toolkit for Quality Stats of data from new illumina pipeline software

    Hi,

    My data is in a new format generated by the new illumina pipeline software v 1.8. So, the quality scores are in Sanger FASTQ format with ASCII offset 33.

    I used following code of Fastx tooklit to find quality stats of my data.

    root@SNP215-01:Cold_Shock_Filtered# fastx_quality_stats -Q33 -i Cold_Shock_negative_2.fq -o Cold_Shock_negative_2.fq.stats

    I received the following ERROR message:

    fastx_quality_stats: Invalid quality score value (char 'J' ord 74 quality value 41) on line 20

    So, please help me to resolve this problem.

    Thank you for your time !

    Vedbar
  • maubp
    Peter (Biopython etc)
    • Jul 2009
    • 1544

    #2
    Illumina also improved the chemistry, so the PHRED score of 41 is real but higher that people are used to, 0 - 40.

    I thought fastx fixed this - which version are you using?

    Comment

    • vedbar
      Junior Member
      • May 2011
      • 5

      #3
      I am using FASTX toolkit 0.0.12.

      Comment

      • swbarnes2
        Senior Member
        • May 2008
        • 910

        #4
        Something like:

        sed s/J/I/ oldfastq.fq > newfastq.fq
        Will change all the 'J's to 'I's; that's a quick and dirty workaround. You'll be slightly lying about how awesomely high quality your letters are, because J's are a little better than I's, but it shouldn't make much difference.

        Comment

        • maubp
          Peter (Biopython etc)
          • Jul 2009
          • 1544

          #5
          Originally posted by vedbar View Post
          I am using FASTX toolkit 0.0.12.
          According to http://hannonlab.cshl.edu/fastx_toolkit/ the latest release is FASTX 0.0.13, but that doesn't explicitly mention this issue. Given the release date (Feb 2010) then I doubt it will cope.

          So try v0.0.13 and if it also fails please contact the FASTX authors.

          Comment

          • kmcarr
            Senior Member
            • May 2008
            • 1181

            #6
            Originally posted by maubp View Post
            According to http://hannonlab.cshl.edu/fastx_toolkit/ the latest release is FASTX 0.0.13, but that doesn't explicitly mention this issue. Given the release date (Feb 2010) then I doubt it will cope.

            So try v0.0.13 and if it also fails please contact the FASTX authors.
            Yes, v0.0.13 does fix this problem. See this thread/post for a more detailed explanation:

            Discussion of next-gen sequencing related bioinformatics: resources, algorithms, open source efforts, etc

            Comment

            • vedbar
              Junior Member
              • May 2011
              • 5

              #7
              Thank you !

              Comment

              Latest Articles

              Collapse

              • SEQadmin2
                Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
                by SEQadmin2



                CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

                Despite this, “CRISPR helped turn genome editing from a specialized technique into
                ...
                07-31-2026, 11:01 AM
              • SEQadmin2
                Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
                by SEQadmin2


                Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

                The systematic characterization of the human proteome has
                ...
                07-20-2026, 11:48 AM

              ad_right_rmr

              Collapse

              News

              Collapse

              Topics Statistics Last Post
              Started by SEQadmin2, 08-13-2026, 12:22 PM
              0 responses
              31 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 08-11-2026, 10:35 AM
              0 responses
              24 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 08-06-2026, 07:41 AM
              0 responses
              38 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 08-03-2026, 10:13 AM
              0 responses
              51 views
              0 reactions
              Last Post SEQadmin2  
              Working...