Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • a_mt
    Member
    • Jul 2012
    • 34

    #1

    fastq with reads missing 3rd line

    Hi all,
    I have a set of fastq files. Some of the fastq files have reads which are missing the 3rd line (which begins with +).

    Code:
    @HWI-ST750:151:C1C6AACXX:5:2316:17997:100881 1:N:0:
    AGCGGTNCGCAATATTTTAGTAGCTCGTTACAGTCCGGTGCGTTTTTGGTTTTTTGAAAGTGCGTCTTCAGAGCGCTTTTGGTTTTCAAAAGCGCTCTGAAGTT+
    1:+B+0#2<DDDDIIIIIIFIIIIIIIIIIIIIEEIID?DDDBBADIII@DDDDD@@AAAAAAA??A?ADAAAA?????A>?8<>?>AAAAA8>>?><AAAA:4
    @HWI-ST750:151:C1C6AACXX:5:2316:19129:100793 1:N:0:
    AGCGCTNCTTGATATCAATCAACTGCTAGACAAATCCAATAGTAAATTGGGTAAACCAAATCTCGATATCGACAGCAAAGTATCACAATATGCCTATAACTACA+
    ;1=DD?#2ACDDDIDEEIIIEIEIEIEEIIIIDEIEIIIDEDDCEDDDEID?BBDIDIIIIEECDIDA@DD=A?D@DAAAA@DDDA>AAABE>AAAA>A>A>AA
    @HWI-ST750:151:C1C6AACXX:5:2316:19695:100854 1:N:0:
    AGCGCTNCACCGCGGTAAGCTTTAGCAGATCTCACTTTGTCTAGCGTTTGAACCATGTTTTCAAGGATATTGGCTCTAAGTTGTGGGTATTTTTCGATCACTTC+
    @<1DDD#2<DFDDGI@CEEGHIIIIIIIEGIIHCGHIIIHGGIGIIAFFHFHAHHIG?CCHFHEEBBC@CDCCCCACCCC5>CCBBB'>ACDECCBBDB7?CC>
    And also sequence line contains the + at the end. I guess 3rd line has been concatenated to the end of 2nd line.
    Any thoughts on how to proceed with this kind of data?? Any scripts to change it into proper format ??
  • jiaco
    Member
    • May 2010
    • 35

    #2
    If this problem is consistent throughout the file

    Code:
    sed "s/+$/\\`echo -e '\n\r'`+/g" bad.fastq > good.fastq
    should do the trick.

    EDIT: never remember adding a newline with sed to be complicated like that, but just tested on a mac and this was required. Maybe on linux it is simpler but I do not have a system here to test.
    Last edited by jiaco; 12-22-2012, 12:16 AM.

    Comment

    • a_mt
      Member
      • Jul 2012
      • 34

      #3
      Thanks for the snippet jiaco.
      Even I had tried this before but this aslso messes up with quality score line which are ending with +

      And also there are reads having empty lines in between. My question is what is the source of this kind of output?? Is this some sort of of sequencing error ??

      Code:
      @@1D4A#2AFHHFIHIIIIIIIIIIIIIIIIIBHHIIIIIIIIIIIIIIIIIIIIIIIDEHIIIHFFHFEEBDEEECCCBBBCC?CB?CCCBBBBB@BBBBBBB/1
      
      @HWI-ST750:151:C1C6AACXX:5:2316:9996:50328/1
      GGCCCCNATACATTTACTGATTCATCCTCAGCGGACTCTGATATGACATCCACTAAAAAATATGTCAGACCACCACCAATGTTAACCTCACCTAATGACTTTCC+
      =71?A@#23CDCD@E@ED?FEFCEI<ECFEA>CDDD6?BDEEC9<DBEEIC<BEEIE3@8?;=>?BA>A:(;;@;=???3:>>D####################/1
      
      @HWI-ST750:151:C1C6AACXX:5:2316:9999:44022/1
      GGCCACNATCTCGATAATTATAAGATATCTTTAGCACAGGCAAATTGGAACGCAAGCGAAGTTTCGAAAAAGCTAGTAAATATTCAAACAGATGGGTCTATTTC+
      ???D;B#2ADDDDIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIEIIIIIIIIIIID?CDEDDD@AAA?AAAADEAEEDDDEDBA?AAAAA?A>?ADDD3/1

      Comment

      • jiaco
        Member
        • May 2010
        • 35

        #4
        You could expand the expression to match
        Code:
        /^[ACGT].*+$/
        to avoid quality lines, but I have no idea where you got the file, let alone how it got corrupted.

        EDIT: saw your new example just now, there is an issue with this file. Maybe someone else has seen it before.
        But I would not try to fix this mess. You need to re-acquire the data.

        Comment

        • a_mt
          Member
          • Jul 2012
          • 34

          #5
          Yes, sequence files were given to me by our sequence provider, which I demultiplexed. But after demultiplexing this is the result. May be there is an issue with this. Anyways I will contact them. Thanks for the suggestion.

          Comment

          • sklages
            Senior Member
            • May 2008
            • 628

            #6
            How do the original files look like? Format?
            How did you multiplex? What program?

            Sven

            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, 08-06-2026, 07:41 AM
            0 responses
            14 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 08-03-2026, 10:13 AM
            0 responses
            31 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 07-31-2026, 02:55 AM
            0 responses
            40 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 07-24-2026, 12:17 PM
            0 responses
            26 views
            0 reactions
            Last Post SEQadmin2  
            Working...