Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • eric.yu
    Junior Member
    • Jul 2013
    • 2

    #1

    tophat: option --read-gap-length not recognized?

    Hi,

    I'm really new to this so please bear with me if I made some really silly mistakes.

    Here's my code for tophat:
    tophat -p 8 --bowtie1 -G path --no-novel-juncs --read-mismatches 4 --read-gap-length 3 --read-edit-dist 2 -o path path &

    and it gave me error :
    tophat: option --read-gap-length not recognized

    Any advice'd be appreciated thanks!
    Last edited by eric.yu; 07-10-2013, 01:11 PM.
  • chadn737
    Senior Member
    • Jan 2009
    • 392

    #2
    1) What version of tophat are you running.....are you sure you have tophat2? Try typing tophat --version to see what version you have.

    2) Secondly, that command wouldn't work anyhow. --read-mismatches and --read-gap-length cannot exceed the value of --read-edit-dist. If you want to set the read-mismatches to 4 an --read-gap-length to 3, then you also have to set the read-edit-dist to 4 or more.
    Last edited by chadn737; 07-10-2013, 03:16 PM.

    Comment

    • eric.yu
      Junior Member
      • Jul 2013
      • 2

      #3
      Originally posted by chadn737 View Post
      1) What version of tophat are you running.....are you sure you have tophat2? Try typing tophat --version to see what version you have.

      2) Secondly, that command wouldn't work anyhow. --read-mismatches and --read-gap-length cannot exceed the value of --read-edit-dist. If you want to set the read-mismatches to 4 an --read-gap-length to 3, then you also have to set the read-edit-dist to 4 or more.

      Thanks for your reply.
      It's 2.0.4
      and also tried
      tophat -p 8 --bowtie1 -G $home/Genes/genes.gtf --no-novel-juncs --read-mismatches 4 --read-gap-length 3 --read-edit-dist 4 -o $home/C1_thout3 $home/BowtieIndex/genome $home/Sample_C1.R1_trimmed.fq.gz &

      still doesn't run

      Comment

      • jp.
        Senior Member
        • Jul 2013
        • 142

        #4
        Hi Senior Member
        I have used tophat successfully with default functions. however, this time I got problem. How to give commands for read length 101 x 2 with insert sixe 80~380(main 150) ?
        I am totally confused


        Originally posted by chadn737 View Post
        1) What version of tophat are you running.....are you sure you have tophat2? Try typing tophat --version to see what version you have.

        2) Secondly, that command wouldn't work anyhow. --read-mismatches and --read-gap-length cannot exceed the value of --read-edit-dist. If you want to set the read-mismatches to 4 an --read-gap-length to 3, then you also have to set the read-edit-dist to 4 or more.

        Comment

        • westerman
          Rick Westerman
          • Jun 2008
          • 1104

          #5
          Originally posted by jp. View Post
          Hi Senior Member
          I have used tophat successfully with default functions. however, this time I got problem. How to give commands for read length 101 x 2 with insert sixe 80~380(main 150) ?
          I am totally confused
          I presume that you've looked at --mate-inner-distance plus --mate-std-dev and are just having a hard time figuring out that the numbers should be. Here are two relevant seqanswer posts that should help:

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


          and

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

          Comment

          • jp.
            Senior Member
            • Jul 2013
            • 142

            #6
            Thank you so much for your help. I got the answer. negative value can be given for --mate-inner-distance.
            Great help for me, thanks


            Originally posted by westerman View Post
            I presume that you've looked at --mate-inner-distance plus --mate-std-dev and are just having a hard time figuring out that the numbers should be. Here are two relevant seqanswer posts that should help:

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


            and

            http://seqanswers.com/forums/showthread.php?t=4355

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