Seqanswers Leaderboard Ad

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • get wrong when I do de novo assembly by trinity for two 22.6G reads file

    Hello,everyone.

    I am using Trinity(v2012-06-08) for de novo assembly, and the size of paired end reads files is 45.1G (2*22.6G), I used the followed command to do this:
    perl Trinity.pl --seqType fq --JM 80G --left mixed_1.fq --right mixed_2.fq --min_contig_length 200 --CPU 10

    but this message was gived back to me:

    Error, the Chrysalis process failed:
    Error, cmd: /home/mbl/softwares/trinityrnaseq_r2012-06-08/Chrysalis/Chrysalis -i both.fa -iworm /home/mbl/softwares/trinityrnaseq_r2012-06-08/trinity_out_dir/inchworm.K25.L25.DS.fa -o chrysalis -cpu 10 -min_glue 2 -min_iso_ratio 0.05 -glue_factor 0.05 -weldmer_size 48 -min 200 -dist 500 -max_reads 20000000 -max_mem_reads 1000000 -paired -butterfly /home/mbl/softwares/trinityrnaseq_r2012-06-08/Butterfly/Butterfly.jar 2>&1 died with ret 65280 at Trinity.pl line 1128.
    at Trinity.pl line 808
    main::run_chrysalis('/home/mbl/softwares/trinityrnaseq_r2012-06-08/trinity_out_dir...', 'both.fa', 200, 500, undef) called at Trinity.pl line 681


    what happened? Who can help me?

  • #2
    Is there a message before the one you mention? Basically the message you gave is from Trinity.pl. What we need the is the message from Chrysalis.

    Comment


    • #3
      Originally posted by westerman View Post
      Is there a message before the one you mention? Basically the message you gave is from Trinity.pl. What we need the is the message from Chrysalis.
      Yes, there is a error message before taht one:

      CMD: /home/mbl/softwares/trinityrnaseq_r2012-06-08/Chrysalis//../util/alignReads.pl --target /home/mbl/softwares/trinityrnaseq_r2012-06-08/trinity_out_dir/inchworm.K25.L25.DS.fa --aligner bowtie --seqType fa --single both.fa -o iworm_bowtie --retain_SAM_files -- -a -m 20 --best --strata --threads 10 --quiet --chunkmbs 512
      Error, path to required bowtie-build cannot be found at /home/mbl/softwares/trinityrnaseq_r2012-06-08/Chrysalis//../util/alignReads.pl line 206.
      COMMAND: /home/mbl/softwares/trinityrnaseq_r2012-06-08/Chrysalis//../util/alignReads.pl --target /home/mbl/softwares/trinityrnaseq_r2012-06-08/trinity_out_dir/inchworm.K25.L25.DS.fa --aligner bowtie --seqType fa --single both.fa -o iworm_bowtie --retain_SAM_files -- -a -m 20 --best --strata --threads 10 --quiet --chunkmbs 512
      Died with exit code 256
      Exiting.
      time(seconds) unlimited
      file(blocks) unlimited
      data(kbytes) unlimited
      stack(kbytes) unlimited
      coredump(blocks) 0
      memory(kbytes) unlimited
      locked memory(kbytes) 64
      process 772865
      nofiles 1024
      vmemory(kbytes) unlimited
      locks unlimited

      Comment


      • #4
        have you installed bowtie?

        It seems as if Trinity can't font Bowtie. Do you have it installed and in yout $PATH?

        when you type 'which bowtie-build' on the command line, what does it say?

        Matt

        Comment


        • #5
          Originally posted by peromhc View Post
          It seems as if Trinity can't font Bowtie. Do you have it installed and in yout $PATH?

          when you type 'which bowtie-build' on the command line, what does it say?

          Matt


          both bowtie and bowtie2 bave been installed and in the $PATH
          I tried trinity again and it seens that bowtie2 make a mistake, when I change to use bowtie1, it's OK

          Comment

          Latest Articles

          Collapse

          • noor121
            Reply to Latest Developments in Precision Medicine
            by noor121
            Qadri offers efficient online services designed for students and staff of University Targu Mures Medical Campus Hamburg. We streamline your academic and administrative processes for a hassle-free experience.

            VIsit us:
            https://qadri-international.com/univ...s-hamburg-umch...
            Today, 09:33 PM
          • seqadmin
            Non-Coding RNA Research and Technologies
            by seqadmin




            Non-coding RNAs (ncRNAs) do not code for proteins but play important roles in numerous cellular processes including gene silencing, developmental pathways, and more. There are numerous types including microRNA (miRNA), long ncRNA (lncRNA), circular RNA (circRNA), and more. In this article, we discuss innovative ncRNA research and explore recent technological advancements that improve the study of ncRNAs.

            Nobel Prize for MicroRNA Discovery
            This week,...
            Yesterday, 08:07 AM
          • seqadmin
            Recent Developments in Metagenomics
            by seqadmin





            Metagenomics has improved the way researchers study microorganisms across diverse environments. Historically, studying microorganisms relied on culturing them in the lab, a method that limits the investigation of many species since most are unculturable1. Metagenomics overcomes these issues by allowing the study of microorganisms regardless of their ability to be cultured or the environments they inhabit. Over time, the field has evolved, especially with the advent...
            09-23-2024, 06:35 AM

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by seqadmin, 10-02-2024, 04:51 AM
          0 responses
          96 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 10-01-2024, 07:10 AM
          0 responses
          107 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 09-30-2024, 08:33 AM
          1 response
          109 views
          0 likes
          Last Post EmiTom
          by EmiTom
           
          Started by seqadmin, 09-26-2024, 12:57 PM
          0 responses
          20 views
          0 likes
          Last Post seqadmin  
          Working...
          X