Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • genome1
    Member
    • Oct 2013
    • 12

    Tophat2: OSError: [Errno 2] No such file or directory

    I am having a trouble while running tophat2.
    I am using tophat2 (v2.0.11), Bowtie2 (v2.2.2) and samtools (v0.1.19).
    The command line that I am using is as follows:
    $ tophat -G /path/to/Homo_sapiens/Ensembl/GRCh37/Annotation/Genes/genes.gtf --transcriptome-index /path/to/transcriptome_data/known -o /path/to/out -p 8 /path/to/Homo_sapiens/Ensembl/GRCh37/Sequence/Bowtie2Index/genome /path/to/read_1.fastq.gz /path/to/read_2.fastq.gz

    The last few lines of the error message is:

    [2014-04-18 01:59:45] Resuming TopHat pipeline with unmapped reads
    Traceback (most recent call last):
    File "./tophat", line 4084, in <module>
    sys.exit(main())
    File "./tophat", line 4050, in main
    user_supplied_deletions)
    File "./tophat", line 3452, in spliced_alignment
    if not nonzeroFile(initial_reads[0]) and \
    File "./tophat", line 1159, in nonzeroFile
    samtools_view = subprocess.Popen(samtools_view_cmd, stdout=subprocess.PIPE)
    File "/usr/lib64/python2.6/subprocess.py", line 642, in __init__
    errread, errwrite)
    File "/usr/lib64/python2.6/subprocess.py", line 1234, in _execute_child
    raise child_exception
    OSError: [Errno 2] No such file or directory

    Can anyone of you help me to solve the problem.
    Thank you.
  • dpryan
    Devon Ryan
    • Jul 2011
    • 3478

    #2
    Was the disk you were using full? It's trying to open a file that it should have just created but can't. The most likely explanation is that the disk is full.

    Comment

    • genome1
      Member
      • Oct 2013
      • 12

      #3
      No there were enough space in the disk. Now the problem has been resolved.
      I have replaced tophat with tophat2 in the command line.

      Comment

      • konika
        Member
        • Sep 2010
        • 14

        #4
        Tophat error about samtools version

        Hi
        I have tried using tophat2 but still got a similar error
        tophat2 -r 20 test_ref reads_1.fq reads_2.fq

        [2014-10-15 12:50:45] Beginning TopHat run (v2.0.11)
        -----------------------------------------------
        [2014-10-15 12:50:45] Checking for Bowtie
        Bowtie version: 2.1.0.0
        [2014-10-15 12:50:45] Checking for Samtools
        Traceback (most recent call last):
        File "/appl/bio/tophat/tophat-2.0.11.Linux_x86_64/tophat", line 4084, in <module>
        sys.exit(main())
        File "/appl/bio/tophat/tophat-2.0.11.Linux_x86_64/tophat", line 3882, in main
        check_samtools()
        File "/appl/bio/tophat/tophat-2.0.11.Linux_x86_64/tophat", line 1556, in check_samtools
        samtools_version_str, samtools_version_arr = get_samtools_version()
        File "/appl/bio/tophat/tophat-2.0.11.Linux_x86_64/tophat", line 1538, in get_samtools_version
        samtools_version_arr = [int(version_match.group(x)) for x in [1,2,3]]
        AttributeError: 'NoneType' object has no attribute 'group'


        Any ideas?
        Thanks

        Comment

        • GenoMax
          Senior Member
          • Feb 2008
          • 7142

          #5
          Are you using new samtools (v.1.x) by chance? TopHat is likely incompatible with the latest samtools (they are now bundling an older version of samtools in TopHat downloads).

          You are running an old Tophat version BTW (current is v.2.0.13).

          Comment

          • konika
            Member
            • Sep 2010
            • 14

            #6
            Thanks, I used the older version of samtools and it fixed.

            Comment

            Latest Articles

            Collapse

            • GATTACAT
              Reply to Nine Things a Sample Prep Scientist Thinks About Before Sequencing
              by GATTACAT
              Love this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
              07-01-2026, 11:43 AM
            • SEQadmin2
              Nine Things a Sample Prep Scientist Thinks About Before Sequencing
              by SEQadmin2


              I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.

              Here are nine questions we think about, in roughly the order they matter, before...
              06-18-2026, 07:11 AM

            ad_right_rmr

            Collapse

            News

            Collapse

            Topics Statistics Last Post
            Started by SEQadmin2, 07-02-2026, 11:08 AM
            0 responses
            14 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 06-30-2026, 05:37 AM
            0 responses
            15 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 06-26-2026, 11:10 AM
            0 responses
            20 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 06-17-2026, 06:09 AM
            0 responses
            54 views
            0 reactions
            Last Post SEQadmin2  
            Working...