Seqanswers Leaderboard Ad

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • Tophat trouble reconstituting index

    Hi all,

    I'm new to the field so please forgive my ignorance. I setup Tophat, Bowtie, and SamTools and attempted to run tophat on some samples. This is the message it produced:

    [2012-11-28 19:56:55] Beginning TopHat run (v2.0.6)
    -----------------------------------------------
    [2012-11-28 19:56:55] Checking for Bowtie
    Bowtie 2 not found, checking for older version..
    Bowtie version: 0.12.8.0
    [2012-11-28 19:56:55] Checking for Samtools
    Samtools version: 0.1.18.0
    [2012-11-28 19:56:55] Checking for Bowtie index files
    [2012-11-28 19:56:55] Checking for reference FASTA file
    [2012-11-28 19:56:55] Generating SAM header for /u/home/mcdb/x/bowtie-0.12.8/indexes/genome
    format: fastq
    quality scale: phred64 (reads generated with GA pipeline version >= 1.3)
    [2012-11-28 19:58:09] Reading known junctions from GTF file
    [2012-11-28 19:58:21] Preparing reads
    left reads: min. length=50, max. length=50, 75848803 kept reads (6201 discarded)
    [2012-11-28 20:17:00] Creating transcriptome data files..
    [FAILED]
    Error: gtf_to_fasta returned an error.
    open: No such file or directory
    [main_samview] fail to open "R1/accepted_hits.bam" for reading.
    cp: cannot stat `R1/accepted_hits.bam': No such file or directory

    This is a different error than I first posted, sorry. I can't figure out why I am getting the gtf_to_fasta error. I downloaded Ensembl's NCBIM37 for mouse here: http://cufflinks.cbcb.umd.edu/igenomes.html. Then I used the mus_musculus gtf included in it, as well as the genome.ebwt files included in the BowtieIndex folder of the unpacked file. I read in another post that this error could be from the fasta and gtf files having different names, so I renamed them both genome but got the same error.


    Any help is appreciated. Thanks!
    Last edited by Xinlitik; 11-28-2012, 09:03 PM.

  • #2
    Can your post your command? It looks like it having trouble just finding the file. You might double check that the paths are correct?

    Comment


    • #3
      Originally posted by Wallysb01 View Post
      Can your post your command? It looks like it having trouble just finding the file. You might double check that the paths are correct?
      Thanks for the reply. I "fixed" the problem by pilfering a labmate's gtf and .ewbt files. The ebwt files had identical sizes so that was just to be safe, so the different GTF must have been the problem. The thing is, I don't know why, hah. Any reason why the GTF included in the link in my first post would not work? The one I used successfully was also ensembl (mm9.ensembl.gtf) so I'm not sure why it failed. Does filename matter? Should I have tried e.g. genome.ensembl.gtf to go with genome.ewbt1234?

      Here is the command:

      tophat --solexa1.3-quals --no-coverage-search -g 1 -G /u/home/mcdb/dashraf/GTF/mm9.ensembl.gtf -p 8 -o ./$k /u/home/mcdb/x/bowtie-0.12.8/indexes/temp/mm9 $k.fastq

      (the /temp/ is because I added the labmate ewbts in a new folder)

      Comment

      Latest Articles

      Collapse

      • seqadmin
        Advancing Precision Medicine for Rare Diseases in Children
        by seqadmin




        Many organizations study rare diseases, but few have a mission as impactful as Rady Children’s Institute for Genomic Medicine (RCIGM). “We are all about changing outcomes for children,” explained Dr. Stephen Kingsmore, President and CEO of the group. The institute’s initial goal was to provide rapid diagnoses for critically ill children and shorten their diagnostic odyssey, a term used to describe the long and arduous process it takes patients to obtain an accurate...
        12-16-2024, 07:57 AM
      • seqadmin
        Recent Advances in Sequencing Technologies
        by seqadmin



        Innovations in next-generation sequencing technologies and techniques are driving more precise and comprehensive exploration of complex biological systems. Current advancements include improved accessibility for long-read sequencing and significant progress in single-cell and 3D genomics. This article explores some of the most impactful developments in the field over the past year.

        Long-Read Sequencing
        Long-read sequencing has seen remarkable advancements,...
        12-02-2024, 01:49 PM

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by seqadmin, 12-17-2024, 10:28 AM
      0 responses
      32 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 12-13-2024, 08:24 AM
      0 responses
      48 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 12-12-2024, 07:41 AM
      0 responses
      34 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 12-11-2024, 07:45 AM
      0 responses
      46 views
      0 likes
      Last Post seqadmin  
      Working...
      X