Unconfigured Ad

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

    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
              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
            • SEQadmin2
              From Collection to Sequencing: Why Sample Preparation and Preservation Define Sequencing Data
              by SEQadmin2


              Data variability is still an issue in sequencing technologies despite the advances in reproducibility and accuracy of these platforms. But the problem does not originate in the sequencing itself, but in the previous steps, before the sample reaches the sequencer.


              The first step is collection, followed by preservation and sample preparation for analysis. Most scientists overlook those steps, but not being careful might just be skewing the experiment’s results.
              ...
              06-02-2026, 10:05 AM

            ad_right_rmr

            Collapse

            News

            Collapse

            Topics Statistics Last Post
            Started by SEQadmin2, Yesterday, 11:10 AM
            0 responses
            7 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 06-17-2026, 06:09 AM
            0 responses
            42 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 06-09-2026, 11:58 AM
            0 responses
            103 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 06-05-2026, 10:09 AM
            0 responses
            125 views
            0 reactions
            Last Post SEQadmin2  
            Working...