Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • ojham
    Member
    • May 2012
    • 16

    #1

    Bowtie Output

    Hello everyone,
    Is it possible to get fastq file as an output file of bowtie tool ?

    Thanks.
  • dpryan
    Devon Ryan
    • Jul 2011
    • 3478

    #2
    Normally you would feed bowtie a fastq file as input. Presumably you want a fastq file of the unmapped reads or something like that. Just use the -un flag and supply a file name. If, for some reason, you want the aligned reads (or all of them for that matter) from a SAM file in fastq format, you could just write a trivial shell script to do so (presumably this is also true of the original bowtie output format, which I've never used).

    Comment

    • ojham
      Member
      • May 2012
      • 16

      #3
      Hi, thank you for the response. I need unmapped reads from bowtie output. Can you please, explain using of -un flag in detail. Thank You.
      Last edited by ojham; 07-03-2012, 11:27 AM.

      Comment

      • dpryan
        Devon Ryan
        • Jul 2011
        • 3478

        #4
        Have you looked at the appropriate section of the manual page for bowtie1 or bowtie2 (depending on the version you're using)? BTW, you may want --un-conc instead, depending on your reads.

        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
        17 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...