Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • cbaudo
    Member
    • Jan 2013
    • 21

    #1

    Cuffmerge error

    Hello, I am getting the following error message when using Cuffmerge:

    cas-mw134-9sb9s:cufflinks-2.2.1.OSX_x86_64 bioadmin$ ./cuffmerge —p 30 -g genes_sort.gtf -s reference.txt assembly.txt

    [Tue Mar 31 12:17:12 2015] Beginning transcriptome assembly merge
    -------------------------------------------

    [Tue Mar 31 12:17:12 2015] Preparing output location ./merged_asm/
    Traceback (most recent call last):
    File "./cuffmerge", line 580, in <module>
    sys.exit(main())
    File "./cuffmerge", line 530, in main
    transfrag_list_file = open(args[0], "r")
    IOError: [Errno 2] No such file or directory: '\xe2\x80\x94p'

    The assembly.txt file contains path information for the cufflinks output:
    /Users/bioadmin/Desktop/cufflinks_results/2R4/transcripts.gtf
    /Users/bioadmin/Desktop/cufflinks_results/2R5/transcripts.gtf
    /Users/bioadmin/Desktop/cufflinks_results/2R6/transcripts.gtf
    etc.

    The log out file simply contains the command I entered into terminal. I'm using a system with 40GB of memory and 8 CPUs. Could you please help me identify the issue?
  • sshankr
    Junior Member
    • Sep 2015
    • 2

    #2
    Hello cbaudo,

    I am facing a similar issue with Cuffmerge. The runs terminate within a sec and the run.log file only contains the command which I executed.

    Were you able to resolve this issue?

    Comment

    • sshankr
      Junior Member
      • Sep 2015
      • 2

      #3
      I was able to rectify this by specifying the -o option at the beginning, after cuffmerge.

      Comment

      • alexGrenoble
        Junior Member
        • Nov 2013
        • 2

        #4
        is there a specific reason that different genes merge together in cuffmerge? Just because they are close to each other?

        What I have is 3 different genes, that have the same assembled merged gene ID but have different transcripts.

        I was expecting that since cuffmerge merges the gene IDs, it would merge the transcripts as well, and this could have been the reason that it merges the genes together. But in my case I get different assembled merged transcript IDs.

        Any idea why?

        Comment

        Latest Articles

        Collapse

        • SEQadmin2
          Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
          by SEQadmin2



          CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

          Despite this, “CRISPR helped turn genome editing from a specialized technique into
          ...
          Yesterday, 11:01 AM
        • SEQadmin2
          Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
          by SEQadmin2


          Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

          The systematic characterization of the human proteome has
          ...
          07-20-2026, 11:48 AM
        • SEQadmin2
          Advanced Sequencing Platforms Tackle Neuroscience’s Toughest Genomics Problems
          by SEQadmin2



          Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
          ...
          07-09-2026, 11:10 AM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by SEQadmin2, Yesterday, 02:55 AM
        0 responses
        9 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 07-24-2026, 12:17 PM
        0 responses
        12 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 07-23-2026, 11:41 AM
        0 responses
        12 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 07-20-2026, 11:10 AM
        0 responses
        24 views
        0 reactions
        Last Post SEQadmin2  
        Working...