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  • antifolate
    replied
    So I just tried the command again to show you the error message and guess what? It worked!! It's still at 4% but at least it's progressing.

    I checked the earlier run's log file to see why it halted. It's probably because I set max_memory to 30GB. 20GB made it work. Or, it could be just luck.

    Thanks for the help.

    Leave a comment:


  • GenoMax
    replied
    Look at the memory angle. Also it would help to post the exact error you are getting for further diagnosis.

    Leave a comment:


  • antifolate
    replied
    The server I use has 33 Gigs of RAM, but I could be allowed to use only a fraction of that memory because the server is shared. My read file is about 2GB and the error is occurring about 2 minutes after running the command.

    Leave a comment:


  • GenoMax
    replied
    Trinity requires significant amount of RAM. How much do you have available on the machine you are running this on? Does the error occur right away? What size is your input dataset?

    Leave a comment:


  • antifolate
    replied
    Originally posted by GenoMax View Post
    What is in this file: your_sample_name.output.qtrim.fq.readcount?
    This number 8568633

    Leave a comment:


  • GenoMax
    replied
    What is in this file: your_sample_name.output.qtrim.fq.readcount?

    Leave a comment:


  • antifolate
    replied
    I'm having this same problem. Help

    Leave a comment:


  • sahusarika
    started a topic Trinity Error

    Trinity Error

    Hello All

    I am using Trinity for assembly i have prob
    Monday, May 25, 2015: 12:29:04 CMD: /home/user/Desktop/sarika/trinityrnaseq-2.0.6/trinity-plugins/fastool/fastool --illumina-trinity --to-fasta seq_cr1.output.qtrim.fq >> single.fa 2> seq_cr1.output.qtrim.fq.readcount
    -------------------------------------------
    ----------- Jellyfish --------------------
    -- (building a k-mer catalog from reads) --
    -------------------------------------------

    Monday, May 25, 2015: 12:29:04 CMD: /home/user/Desktop/sarika/trinityrnaseq-2.0.6/trinity-plugins/jellyfish/bin/jellyfish count -t 6 -m 25 -s 7666907757 --canonical single.fa 2> /dev/null
    bash: line 1: 24275 Aborted (core dumped) /home/user/Desktop/sarika/trinityrnaseq-2.0.6/trinity-plugins/jellyfish/bin/jellyfish count -t 6 -m 25 -s 7666907757 --canonical single.fa 2> /dev/null
    Trinity run failed. Must investigate error above.

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  • 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).

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