Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • bioinfonewbie
    Junior Member
    • Feb 2016
    • 1

    #1

    RSEM prep error

    Hi! I'm new to bioinformatics and I'm learning the ropes.

    I'm trying to estimate abundance following the Trinity-RSEM pipeline. My script goes something like this:

    align_and_estimate_abundance.pl --transcripts $TRANSCRIPTS --seqType fq --left MLGY_L_001.fastq,MLGY_L_002.fastq,MLGY_L_003.fastq,MLGY_L_004.fastq,MLGY_L_005.fastq,MLGY_L_006.fastq --right MLGY_R_001.fastq,MLGY_R_002.fastq,MLGY_R_003.fastq,MLGY_R_004.fastq,MLGY_R_005.fastq,MLGY_R_006.fastq --est_method RSEM --aln_method bowtie --trinity_mode --prep_reference

    I keep on getting the following error:

    WARNING - looks like the prep for /nfs/users/...bowtie was already started by another process. Proceeding with caution.
    CMD: touch /nfs/users/...bowtie.started
    CMD: bowtie-build /nfs/users/...bowtie
    Warning: Empty input file
    Error: No unambiguous stretches of characters in the input. Aborting...
    Command: bowtie-build /nfs/users/...bowtie
    Error, cmd: bowtie-build /nfs/users/...bowtie died with ret: 256 at /apps/trinity/trinity_2.0.6/util/align_and_estimate_abundance.pl line 653.
    srun: error: cfb-smp1: task 0: Exited with exit code 2

    I cannot pinpoint the problem and how to solve it. I already made several attempts at this, the earliest attempts involved separate steps (scripts) for preparing the reference and alignment/estimation. If the prep step error remains like this, is there a way to "reset"?

    (As an aside, I also what to know is there is any real difference between ".fastq" and ".fq" files. I saw online that RSEM can't handle fastq.gz files and I had to uncompressed them to fastq first.)

    I appreciate all the help. Thank you very much!
  • sahusarika
    Junior Member
    • Apr 2015
    • 7

    #2
    RSEM error

    I have run the command
    /opt/software/trinityrnaseq/util/align_and_estimate_abundance.pl --seqType fq --left /home/sahusarikaiiita/trinity_indu/paired_DerivedRapa_R1.fastq --right /home/sahusarikaiiita/trinity_indu/paired_DerivedRapa_R1.fastq --transcripts /home/sahusarikaiiita/trinity_indu/B_rapa_Trinity.fasta --output_prefix bean --est_method RSEM --aln_method bowtie2 --prep_reference

    I hv got the error in rsem
    RSEM is already installed in my server
    CMD: touch /home/sahusarikaiiita/trinity_indu/B_rapa_Trinity.fasta.bowtie2.started
    CMD: bowtie2-build /home/sahusarikaiiita/trinity_indu/B_rapa_Trinity.fasta /home/sahusarikaiiita/trinity_indu/B_rapa_Trinity.fasta.bowtie2
    Building a SMALL index
    CMD: touch /home/sahusarikaiiita/trinity_indu/B_rapa_Trinity.fasta.RSEM.rsem.prepped.started
    CMD: rsem-prepare-reference --no-polyA /home/sahusarikaiiita/trinity_indu/B_rapa_Trinity.fasta /home/sahusarikaiiita/trinity_indu/B_rapa_Trinity.fasta.RSEM
    Invalid number of arguments!

    Comment

    • madhavi
      Member
      • Jan 2015
      • 14

      #3
      Hello guys
      You both just change the command a little bit and try the following command and check.And one more thing please place your reference trinity.fasta directly in the trinity/trinity_2.0.6/util/.
      perl align_and_estimate_abundance.pl --transcripts Trinity.fasta --seqType fq --left R1.fastq --right R2.fastq --est_method RSEM --aln_method bowtie --trinity_mode --prep_reference --output_dir rsem_outdir

      Comment

      Latest Articles

      Collapse

      • 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
      • SEQadmin2
        New Genomics Technologies Take Aim at Long-Standing Limits
        by SEQadmin2


        Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.

        We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing
        ...
        09-28-2026, 10:25 AM

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by SEQadmin2, Yesterday, 11:13 AM
      0 responses
      16 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, Yesterday, 10:48 AM
      0 responses
      15 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-15-2026, 10:52 AM
      0 responses
      35 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-14-2026, 05:39 AM
      0 responses
      42 views
      0 reactions
      Last Post SEQadmin2  
      Working...