Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • peterlchang
    Junior Member
    • Mar 2010
    • 5

    #1

    Is anyone having trouble with tophat's SAM file -> cufflinks?

    I am having trouble running cufflinks on my own SAM file generated from tophat. I used many SAM files generated from real data as well as simulated data, but I can't get cufflinks to assemble the transcripts using any of my SAM files.

    I tried downloading the file: test_data.sam and it works fine. It identifies three exons and notes that they are part of one transcript. When I try this on my SAM file, it identifies all the exons as their own transcripts, even though I see many reads that span the exons.

    Any help would be appreciated. Thanks
  • Siva
    Member
    • Nov 2008
    • 57

    #2
    Did you run Tophat on more than one sequence reads at the same time? If so you might want to run it one at a time. If not, then well, at the moment I can't think of an answer.

    Siva

    Comment

    • peterlchang
      Junior Member
      • Mar 2010
      • 5

      #3
      Would this matter if I specify a different ouuput file for each run?

      I am trying to figure out if the SAM format is a problem or if the actual reads do not cover the junction enough for the transcript to be called.

      Comment

      • peterlchang
        Junior Member
        • Mar 2010
        • 5

        #4
        Actually it is really strange. I cannot get any of my tophat-generated SAM outputs to successfully run using cufflinks (it runs but it lists each exon as its own transcript). I've done this with real data and simulated data.

        Comment

        • Siva
          Member
          • Nov 2008
          • 57

          #5
          Originally posted by peterlchang View Post
          Actually it is really strange. I cannot get any of my tophat-generated SAM outputs to successfully run using cufflinks (it runs but it lists each exon as its own transcript). I've done this with real data and simulated data.
          Hi are u working with an organism whose typical intron size is very large? If so you can change Tophat's default parameters. Cufflinks typically gives you a GTF file detailing FPKM etc, a comma delimited transcript.expr file and a list of gene coordinates (genes.expr).

          Comment

          • peterlchang
            Junior Member
            • Mar 2010
            • 5

            #6
            The gene I am testing is 34K long (ie. the reference sequence is 34K long). The default intron length for tophat is 500K and I changed that parameter to 50K. The default intron length for tophat is 300K, and that was left unchanged.

            In addition, tophat is able to find reads that span the junction. I don't know what the issue could be. I already emailed Cole so I hope he can get back to me asap.

            Thanks

            Comment

            Latest Articles

            Collapse

            • SEQadmin2
              16S/ITS Profiling vs. Shotgun Metagenomics: What Changes in Your Workflow?
              by SEQadmin2




              NGS has revolutionized clinical microbiology by offering new ways to identify and surveil pathogens without prior knowledge of the target. One popular approach is 16S rRNA and ITS amplicon sequencing, which targets specific microbial markers. But studies are increasingly incorporating shotgun metagenomics, a technique that sequences all DNA from a sample without targeting specific microbial markers. This approach allows more detailed taxonomic classification, detection...
              Today, 06:46 AM
            • 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

            ad_right_rmr

            Collapse

            News

            Collapse

            Topics Statistics Last Post
            Started by SEQadmin2, 10-28-2026, 09:57 AM
            0 responses
            23 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 10-28-2026, 09:51 AM
            0 responses
            15 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 10-22-2026, 11:13 AM
            0 responses
            68 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 10-22-2026, 10:48 AM
            0 responses
            48 views
            0 reactions
            Last Post SEQadmin2  
            Working...