Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • zxybl
    Member
    • Apr 2010
    • 13

    #1

    what does this bowtie error information mean?

    I ran bowtie with default parameter. there was an error information:

    Reads file contained a pattern with more than 1024 sequence characters.
    Please truncate reads and quality values and re-run Bowtie.
    Offending read: AIAE-aaa09g07.g1
    Command: bowtie -f can20100804 ../cDNA/ALL_input_reads. clean.contam_free.min_size_50bp.pruned_headers.fna

    what does it mean? How can I truncate the reads?

    Thanks,
    xu
  • zxybl
    Member
    • Apr 2010
    • 13

    #2
    I think this is the answer:
    it supports arbitrarily small reference sequences (e.g. amplicons) and reads as long as 1024 bases
    I will check my reads.

    Comment

    • pepperoni
      Member
      • Oct 2011
      • 59

      #3
      I get the same error and I am sure my longest read is 55bp. What does that mean? how can I solve it? Actually if I convert the fastq file to fasta and run Bowtie it does work with the fasta. I have also got rid of all the reads that contained dots.
      Last edited by pepperoni; 10-18-2011, 09:50 AM.

      Comment

      • Sinha_Ashis
        Junior Member
        • May 2012
        • 2

        #4
        Same error cant find solution

        Hello everyone,

        My name is Ashis. I am quite new here. I run bowtie as well and am getting the same error,

        Reads file contained a pattern with more than 1024 quality values
        Please truncate reads and quality values and and re-run Bowtie

        my friends advised me to get rid of the . (dots) in the reads. but how do I do that, I tried using fastx_clipper but then I get an error

        fastx_clipper: found invalid nucleotide sequence (GTTTCTGATGGATTAGTGGAGAAAACAGAAAATTCTGAGTA#&%%) on line 14364670

        the special characters after AAAATTCTGAGTA ie #&%% are not coming out right


        please help

        Ashis

        Comment

        • zxybl
          Member
          • Apr 2010
          • 13

          #5
          I did not use fastx_clipper. but you can just use a command(such as sed,perl) to remove them. and I think you also need to remove all these characters and make sure the sequence length is less than 1024.

          Good luck



          Originally posted by Sinha_Ashis View Post
          Hello everyone,

          My name is Ashis. I am quite new here. I run bowtie as well and am getting the same error,

          Reads file contained a pattern with more than 1024 quality values
          Please truncate reads and quality values and and re-run Bowtie

          my friends advised me to get rid of the . (dots) in the reads. but how do I do that, I tried using fastx_clipper but then I get an error

          fastx_clipper: found invalid nucleotide sequence (GTTTCTGATGGATTAGTGGAGAAAACAGAAAATTCTGAGTA#&%%) on line 14364670

          the special characters after AAAATTCTGAGTA ie #&%% are not coming out right


          please help

          Ashis

          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, Yesterday, 11:13 AM
          0 responses
          19 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, Yesterday, 10:48 AM
          0 responses
          18 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...