Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • bfp7
    Junior Member
    • Nov 2015
    • 9

    #1

    Trinity question

    I am very new to bioinformatics and trinity. I am getting n error message when I run trinity:

    No command 'Trinity' found, did you mean:
    Command 'trinity' from package 'trinity' (universe)

    anyone?
  • yueluo
    Member
    • Aug 2013
    • 82

    #2
    Use the absolute path to your trinity program or add that directory to your system PATH.

    Comment

    • bfp7
      Junior Member
      • Nov 2015
      • 9

      #3
      thanks for the reply. now I am getting another error message when I try to run trinity.

      This is my command:

      Trinity --output seahorse.trim2.corrected.trinity --full_cleanup --seqType fq --max_memory 20G --left ppart.trim2.inter.cor.fq.1 --right ppart.trim2.inter.cor.fq.2 --CPU 16

      When I do ls -lth the files containing the left and right reads are not empty.

      This is the error message I got:

      Converting input files. (in parallel)Tuesday, November 24, 2015: 03:09:57 CMD: cat /home/ubuntu/trimming/ppart.trim2.inter.cor.fq.1 | /home/ubuntu/trinityrnaseq/trinity-plugins/fastool/fastool --illumina-trinity --to-fasta >> left.fa 2> /home/ubuntu/trimming/ppart.trim2.inter.cor.fq.1.readcount
      Thread 1 terminated abnormally: Error, cmd: cat /home/ubuntu/trimming/ppart.trim2.inter.cor.fq.1 | /home/ubuntu/trinityrnaseq/trinity-plugins/fastool/fastool --illumina-trinity --to-fasta >> left.fa 2> /home/ubuntu/trimming/ppart.trim2.inter.cor.fq.1.readcount died with ret 768 at /home/ubuntu/trinityrnaseq/Trinity line 2183.
      Tuesday, November 24, 2015: 03:09:57 CMD: cat /home/ubuntu/trimming/ppart.trim2.inter.cor.fq.2 | /home/ubuntu/trinityrnaseq/trinity-plugins/fastool/fastool --illumina-trinity --to-fasta >> right.fa 2> /home/ubuntu/trimming/ppart.trim2.inter.cor.fq.2.readcount
      Thread 2 terminated abnormally: Error, cmd: cat /home/ubuntu/trimming/ppart.trim2.inter.cor.fq.2 | /home/ubuntu/trinityrnaseq/trinity-plugins/fastool/fastool --illumina-trinity --to-fasta >> right.fa 2> /home/ubuntu/trimming/ppart.trim2.inter.cor.fq.2.readcount died with ret 768 at /home/ubuntu/trinityrnaseq/Trinity line 2183.
      Trinity run failed. Must investigate error above.

      Comment

      • griff
        Junior Member
        • Feb 2016
        • 4

        #4
        I am having the same problem

        Hi,

        I was wondering whether you had had any luck fixing this as I have just started trying to use trinity and I am getting the same error message!

        Thanks,

        Hannah

        Comment

        • bfp7
          Junior Member
          • Nov 2015
          • 9

          #5
          Hi Hannah,

          The error message was due to a space in the header of the fastq file. Use the more command and the name of your file to look at the header of your fastq file.

          more "name of file"

          Look for a space in the header. I got my data from the European Nucleotide Archive.

          If there is a space in the header you can use the "sed" command to remove it.

          Comment

          • griff
            Junior Member
            • Feb 2016
            • 4

            #6
            Thank you

            thank you so much for this,

            I got my data from ENA and turns out my fastq headers had the same problem! I have used sed and this appears to have sorted this and trinity is now running

            fingers crossed I wont have any more issue.

            Hope your trinity assembly worked well in the end too!!

            Thanks again,

            Hannah

            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
              ...
              07-31-2026, 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

            ad_right_rmr

            Collapse

            News

            Collapse

            Topics Statistics Last Post
            Started by SEQadmin2, 08-13-2026, 12:22 PM
            0 responses
            23 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 08-11-2026, 10:35 AM
            0 responses
            19 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 08-06-2026, 07:41 AM
            0 responses
            33 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 08-03-2026, 10:13 AM
            0 responses
            51 views
            0 reactions
            Last Post SEQadmin2  
            Working...