Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • jjjscuedu
    Member
    • Mar 2012
    • 35

    trinity error

    I try to run the trinity for my RNA-seq dataset, but get the following errors:

    CMD finished (0 seconds)
    CMD: /diag/software/trinityrnaseq_r2012-03-17/Inchworm/bin/inchworm --kmers meryl.kmers.min1.fa --run_inchworm -K 25 -L 48 --monitor 1 > /diag/home/jjin/rice/leaf/test/inchworm.K25.L48.fa.tmp
    /diag/software/trinityrnaseq_r2012-03-17/Inchworm/bin/inchworm: /usr/lib64/libstdc++.so.6: version `GLIBCXX_3.4.11' not found (required by /diag/software/trinityrnaseq_r2012-03-17/Inchworm/bin/inchworm)
    /diag/software/trinityrnaseq_r2012-03-17/Inchworm/bin/inchworm: /usr/lib64/libstdc++.so.6: version `GLIBCXX_3.4.9' not found (required by /diag/software/trinityrnaseq_r2012-03-17/Inchworm/bin/inchworm)
    Error, cmd: /diag/software/trinityrnaseq_r2012-03-17/Inchworm/bin/inchworm --kmers meryl.kmers.min1.fa --run_inchworm -K 25 -L 48 --monitor 1 > /diag/home/jjin/rice/leaf/test/inchworm.K25.L48.fa.tmp died with ret 256 at /diag/software/trinityrnaseq_r2012-03-17/Trinity.pl line 1092.

    ** The inchworm process failed. Below is the tail end of the log file:

    I don't know why i get this error.
    Can anysone give me some suggestions?

    Jingjing
  • BenjaminL
    Junior Member
    • Sep 2010
    • 5

    #2
    compilation errors

    Hallo Jingjing!

    > /usr/lib64/libstdc++.so.6: version `GLIBCXX_3.4.11' not found

    means that the inchworm application is missing a library of the required version. This is a standard system library used for running applications written in c++.

    Most likely the app needs to be recompiled on your system. Or if there is a configuration file, shell variables, etc. that can be changed to match the location of your library files, then that could work.

    Did you compile inchworm on your machine, or download it pre-compiled?
    Benjamin
    Jackson Laboratory for Genomic Medicine

    Comment

    • MalcolmHoutz
      Junior Member
      • Feb 2014
      • 4

      #3
      Trinity can't find /1 or /2 on many reads

      Hi - I am assembling reads using Trinity, which requires a /1 or /2 appended to each left or right hand end of paired reads.
      I appended the /1 and /2 using a perl script, checked my work and let it fly. Trinity complains it can't decipher the /1 or /2 on many reads. It prints the read identifier out for the first 10, then gives a count of the total.

      I grepped the offending records from both the /1 and /2 fastq's, and they look fine.
      Any thoughts?

      Here are the warnings from a tiny test run:

      CMD: rm bowtie.out
      CMD: /share/apps/trinityrnaseq/20131110/Chrysalis//../util/scaffold_iworm_contigs.pl bowtie.nameSorted.sam /scratch/mlh476/rice_project/AZUCENA_trinity_output/inchworm.K25.L25.fa > iworm_scaffolds.txt
      warning, ignoring read: HWI-ST911:1412AWEACXX:4:1101:10008:2437 since cannot decipher if /1 or /2 of a pair.
      warning, ignoring read: HWI-ST911:1412AWEACXX:4:1101:10030:2102 since cannot decipher if /1 or /2 of a pair.
      warning, ignoring read: HWI-ST911:1412AWEACXX:4:1101:10030:2948 since cannot decipher if /1 or /2 of a pair.
      warning, ignoring read: HWI-ST911:1412AWEACXX:4:1101:10044:2925 since cannot decipher if /1 or /2 of a pair.
      warning, ignoring read: HWI-ST911:1412AWEACXX:4:1101:10044:2925 since cannot decipher if /1 or /2 of a pair.
      warning, ignoring read: HWI-ST911:1412AWEACXX:4:1101:10045:2126 since cannot decipher if /1 or /2 of a pair.
      warning, ignoring read: HWI-ST911:1412AWEACXX:4:1101:10066:2279 since cannot decipher if /1 or /2 of a pair.
      warning, ignoring read: HWI-ST911:1412AWEACXX:4:1101:10071:2111 since cannot decipher if /1 or /2 of a pair.
      warning, ignoring read: HWI-ST911:1412AWEACXX:4:1101:10079:2494 since cannot decipher if /1 or /2 of a pair.
      warning, ignoring read: HWI-ST911:1412AWEACXX:4:1101:10082:2037 since cannot decipher if /1 or /2 of a pair.
      warning, ignoring read: HWI-ST911:1412AWEACXX:4:1101:10082:2037 since cannot decipher if /1 or /2 of a pair.
      number of read warnings exceeded 10. Turning off warning messages from here out.
      WARNING: note there were 2829 reads that could not be deciphered as being /1 or /2 of a PE fragment. Hopefully, these were SE reads that should have been ignored. Otherwise, please research this further.

      Comment

      Latest Articles

      Collapse

      • 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
      • SEQadmin2
        Cancer Drug Resistance: The Lingering Barrier to Rising Survival
        by SEQadmin2



        Cancer survival rates have significantly increased in the last few decades in the United States, reaching a combined 70% 5-year survival rate by 2021. Behind this number, there are years of research to find new therapies, drug targets, and early detection methods. But there is one core challenge that keeps slowing down these advances, and it’s about drug resistance.

        There is no single reason why many patients don’t respond to treatment as expected. Cancer is...
        07-08-2026, 05:17 AM

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by SEQadmin2, Today, 12:17 PM
      0 responses
      10 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, Yesterday, 11:41 AM
      0 responses
      11 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 07-20-2026, 11:10 AM
      0 responses
      23 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 07-13-2026, 10:26 AM
      0 responses
      37 views
      0 reactions
      Last Post SEQadmin2  
      Working...