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SEQanswers June Challenge Has Begun!

The competition has begun! We're giving away a $50 Amazon gift card to the member who answers the most questions on our site during the month. We want to encourage our community members to share their knowledge and help each other out by answering questions related to sequencing technologies, genomics, and bioinformatics. The competition is open to all members of the site, and the winner will be announced at the beginning of July. Best of luck!

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  • #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


    • #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


      • #18
        Add execute permissions as above.

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

        Comment


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

          Comment


          • #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


            • #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

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