Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • GenoMax
    Senior Member
    • Feb 2008
    • 7142

    #16
    Find out where trinity is located (likely under trinityrnaseq-2.0.x/Trinity). Replace with a real path (path_to below).
    Code:
    $ chmod a+x /path_to/Trinity

    Comment

    • lupid
      Member
      • Mar 2015
      • 54

      #17
      now almost done but at the end show this
      Code:
      /trinityrnaseq-2.0.6/util/support_scripts/partitioned_trinity_aggregator.pl: Permiso denegado
      Trinity run failed. Must investigate error above.

      Comment

      • GenoMax
        Senior Member
        • Feb 2008
        • 7142

        #18
        Add execute permissions as above.

        Code:
        $ chmod a+x /trinityrnaseq-2.0.6/util/support_scripts/partitioned_trinity_aggregator.pl

        Comment

        • lupid
          Member
          • Mar 2015
          • 54

          #19
          You are great
          Code:
          ##### Done Running Trinity #####

          Comment

          • lupid
            Member
            • Mar 2015
            • 54

            #20
            Hi to all of you again, I get my first the novo transcriptome, done the last week, but when I try to do the RSEM, it fail and say
            CMD: set -o pipefail && bowtie -q --all --best --strata -m 300 --chunkmbs 512 -X 800 -S -p 4 /home/cmeneses/tomas/carpa/trinity_out.Trinity.fasta.bowtie -1 /home/cmeneses/tomas/carpa/PInviernoPool_S2_L001_R1_001r_-N_-a_-q20_-150.fastq -2 /home/cmeneses/tomas/carpa/PInviernoPool_S2_L001_R2_001r_-N_-a_-q20_-150.fastq | samtools view -F 4 -S -b -o PIr.bowtie.bam -
            Too few quality values for read: M01447:54:000000000-A8564:1:1113:13048:8317 1:N:0:2
            are you sure this is a FASTQ-int file?
            terminate called after throwing an instance of 'int'
            bash: line 1: 50810 Aborted (core dumped) bowtie -q --all --best --strata -m 300 --chunkmbs 512 -X 800 -S -p 4 /home/cmeneses/tomas/carpa/trinity_out.Trinity.fasta.bowtie -1 /home/cmeneses/tomas/carpa/PInviernoPool_S2_L001_R1_001r_-N_-a_-q20_-150.fastq -2 /home/cmeneses/tomas/carpa/PInviernoPool_S2_L001_R2_001r_-N_-a_-q20_-150.fastq
            50811 Done | samtools view -F 4 -S -b -o PIr.bowtie.bam -
            Do you know what to do?

            Comment

            • GenoMax
              Senior Member
              • Feb 2008
              • 7142

              #21
              Originally posted by lupid View Post
              Hi to all of you again, I get my first the novo transcriptome, done the last week, but when I try to do the RSEM, it fail and say Do you know what to do?
              Create a new thread for this since the question is no longer related to the original thread (if the following does not fix the problem).

              Your files are in fastq format correct? I would advise changing the "-" character file names to something else. That is likely to get you into trouble with programs, in case they do not parse the names correctly.

              Comment

              Latest Articles

              Collapse

              • SEQadmin2
                16S/ITS Profiling vs. Shotgun Metagenomics: What Changes in Your Workflow?
                by SEQadmin2




                NGS has revolutionized clinical microbiology by offering new ways to identify and surveil pathogens without prior knowledge of the target. One popular approach is 16S rRNA and ITS amplicon sequencing, which targets specific microbial markers. But studies are increasingly incorporating shotgun metagenomics, a technique that sequences all DNA from a sample without targeting specific microbial markers. This approach allows more detailed taxonomic classification, detection...
                Yesterday, 06:46 AM
              • SEQadmin2
                Multiomic Liquid Biopsy: What DNA/RNA Panels Reveal That DNA Alone Can’t
                by SEQadmin2



                Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?

                Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating
                ...
                10-14-2026, 09:55 AM

              ad_right_rmr

              Collapse

              News

              Collapse

              Topics Statistics Last Post
              Started by SEQadmin2, 10-28-2026, 09:57 AM
              0 responses
              31 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 10-28-2026, 09:51 AM
              0 responses
              21 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 10-22-2026, 11:13 AM
              0 responses
              71 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 10-22-2026, 10:48 AM
              0 responses
              48 views
              0 reactions
              Last Post SEQadmin2  
              Working...