Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • NSher
    Junior Member
    • Dec 2011
    • 1

    #1

    Trouble running Tophat & Cufflinks on Galaxy with non-UCSC-supported genome

    I have been trying to run tophat and cufflinks on Prochlorococcus genome (marine cyanobacteria). I am working using Galaxy; I am not a Linux user but rather a "wet' biologist trying to get into bioinformatics on my own).

    I used the FASTA format of the genome available on MicrobesOnline: http://www.microbesonline.org/cgi-bi....cgi?tId=59919

    I used a gtf file that the microbesonline people helped me create from the tab delimited version available on their website.

    However, I am getting FPKMs of zero for everything.

    I wasnt sure whether there is some disconnect between the genome and transcriptome files I am using, or whether the problem is that I am using a regular FASTA genome but not a bowtie index, or something else??? I would really appreciate troubleshooting help as there is very little help out there for people working on non-UCSC organisms!
  • tnabtaf
    Member
    • Jan 2011
    • 53

    #2
    I used the new "USeGalaxy" custom search (http://galaxyproject.org/search/usegalaxy/) and, um, didn't find anything either.

    Try reposting the question to the Galaxy-User mailing list. You can subscribe here: http://lists.bx.psu.edu/listinfo/galaxy-user

    Comment

    • rnaseek
      Member
      • Nov 2011
      • 22

      #3
      Check this, it might solve the problem. Tophat expects chromosome/feature names used in the annotation file to be the same as used in genome sequence/bowtie indices (and possibly same order). For example, if the chromosomes are named like "chr1" in the indices , the annotation file should also have "chr1" (first column) not "1" or "c1". you can check how the chromosomes are named using the command
      "bowtie-inspect --names path2index". And change the annotation file to be the same as in the index files.

      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
      22 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-28-2026, 09:51 AM
      0 responses
      14 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...