Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Trouble With Trim_Galore processing paired reads

    Hello Everyone,

    I am new to this, and have been havigjn soem trouble with trim galore. I think I've reached that point where I cannot see what is causing my error and I thought I would ask you for your colelctive input:

    Here is my trim_galore command:
    ./trim_galore -a AGATCGGAAGAGC -t --paired /media/daveboBaggins/R2_001.fastq /media/daveboBaggins/R1_001.fastq

    I get as an output:
    SUMMARISING RUN PARAMETERS
    ==========================
    Input filename: /media/daveboBaggins/R2_001.fastq
    Quality Phred score cutoff: 20
    Quality encoding type selected: ASCII+33
    Adapter sequence: 'AGATCGGAAGAGC'
    Maximum trimming error rate: 0.1 (default)
    Minimum required adapter overlap (stringency): 1 bp
    Minimum required sequence length for both reads before a sequence pair gets removed: 20 bp
    All sequences will be trimmed by 1 bp on their 3' end to avoid problems with invalid paired-end alignments with Bowtie 1

    Writing final adapter and quality trimmed output to
    R2_001_trimmed.fq


    >>> Now performing quality (cutoff 20) and adapter trimming in a single pass for the adapter sequence: 'AGATCGGAAGAGC' from file


    I get the following error message:
    open3: exec of /home/daveboBaggins/cutadapt-1.2.1/cutadapt -f fastq -e 0.1 -q 20 -O 1 -a AGATCGGAAGAGC /media/daveboBaggins/7_R2_001.fastq failed at /home/daveboBaggins/trim_galore_zip/trim_galore line 453

    I have gone back to line 453 which is as follows:
    open3 (\*WRITER, \*TRIM, \*ERROR, "$path_to_cutadapt -f fastq -e $error_rate -q $cutoff -O $stringency -a $adapter $filename") or die "Failed to launch Cutadapt: $!";

    I have made sure I added the path to cutadapt in the perl code. But still cannot see what I am doing wrong? I have gone back and the pathway to cutadapt is in the $PATH variable. Any suggestions will be much appreciated

    -Dave-Bo Baggins

  • #2
    While we wait for trimgalore folks to chime in (tomorrow) here is something to test:

    Have you checked to make sure that cutadapt has execute permissions?

    Comment


    • #3
      Originally posted by GenoMax View Post
      While we wait for trimgalore folks to chime in (tomorrow) here is something to test:

      Have you checked to make sure that cutadapt has execute permissions?
      That's exactly what I would have asked. When you enter the same path to Cutadapt that you also find within Trim Galore into a command line, e.g.

      /home/user/cutadapt/bin/cutadapt

      do you see the Cutadapt help? If not, you need to get Cutadapt to run before launching Trim Galore.

      Comment


      • #4
        Originally posted by GenoMax View Post
        While we wait for trimgalore folks to chime in (tomorrow) here is something to test:

        Have you checked to make sure that cutadapt has execute permissions?
        Thanks for your reply I appreciate it. I will be in front of my work computer in an hour and change and will check that out

        Dave

        Comment


        • #5
          Thanks a lot, Ill will be looking into this and will get back to you all asap!

          Comment

          Latest Articles

          Collapse

          • seqadmin
            Essential Discoveries and Tools in Epitranscriptomics
            by seqadmin




            The field of epigenetics has traditionally concentrated more on DNA and how changes like methylation and phosphorylation of histones impact gene expression and regulation. However, our increased understanding of RNA modifications and their importance in cellular processes has led to a rise in epitranscriptomics research. “Epitranscriptomics brings together the concepts of epigenetics and gene expression,” explained Adrien Leger, PhD, Principal Research Scientist...
            04-22-2024, 07:01 AM
          • seqadmin
            Current Approaches to Protein Sequencing
            by seqadmin


            Proteins are often described as the workhorses of the cell, and identifying their sequences is key to understanding their role in biological processes and disease. Currently, the most common technique used to determine protein sequences is mass spectrometry. While still a valuable tool, mass spectrometry faces several limitations and requires a highly experienced scientist familiar with the equipment to operate it. Additionally, other proteomic methods, like affinity assays, are constrained...
            04-04-2024, 04:25 PM

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by seqadmin, Yesterday, 08:47 AM
          0 responses
          16 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-11-2024, 12:08 PM
          0 responses
          60 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-10-2024, 10:19 PM
          0 responses
          60 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-10-2024, 09:21 AM
          0 responses
          54 views
          0 likes
          Last Post seqadmin  
          Working...
          X