Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • empyrean
    Member
    • Sep 2010
    • 52

    #1

    Converting 454 reads to illumina reads

    Hello

    i have a pipeline which works with illumina reads. When i convert the 454 reads in to fastq format and give it as input, the pipeline is not working. The average length of the sequence is 350 bp. I am planning to make them in to 100bp reads. Are there any tools out there which can do this?
  • DFJ111
    Member
    • Aug 2012
    • 20

    #2
    I'm not sure it's a good idea, what are you doing in your pipeline? If your pipeline assumes that all sequences are the same length (as Illumina reads are) it might have issues with the variable read lengths of 454.454 reads also have a lot of associated info (e.g. adaptors, multiplexing tags, suggested end-clips) which are useful to keep. Also not sure why you'd want to throw out an average of 250bp of sequence per read.

    I can think of a lot of other details that might cause the pipeline to break, it really depends what you are doing with the reads. Can you provide more details?

    Comment

    • maasha
      Senior Member
      • Apr 2009
      • 153

      #3
      I am also not convinced it is a good idea to sacrifice all that information, but if you must you can use Biopieces (www.biopieces.org):

      Code:
      read_sff -i data.sff | extract_seq -l 100 | write_fastq -o data.fq -x
      or

      Code:
      read_454 -i data.fna -q data.qual | extract_seq -l 100 | write_fastq -o data.fq -x

      Comment

      • DZhang
        Senior Member
        • Jun 2010
        • 177

        #4
        Hi empyrean,

        Can you share what you plan to achieve? There may be a way to use 454 reads as is to achieve what you want. Or at least help us understand why you want to stick to your Illumina pipeline.

        Best regards,
        Douglas

        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
        55 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-22-2026, 10:48 AM
        0 responses
        40 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-15-2026, 10:52 AM
        0 responses
        46 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-14-2026, 05:39 AM
        0 responses
        46 views
        0 reactions
        Last Post SEQadmin2  
        Working...