Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • FastX tool :: fastq_quality_filter

    Dear All,
    i am doing quality filtering of my fastq file using fastq_quality_filter
    and i am getting this error
    Premature End-Of-File (filename ='-')
    my code is
    nohup fastq_quality_filter ‐v ‐q 20 ‐p 100 -Q33 ‐i GO06_2500_Mate.read2.fastq ‐o Read2.filteredQ20.GO06.fastq > fastq_quality_filterlog &

    my fastq look like
    @GO06_2500_Mate:1_4_72/2
    NGAAGGGTGGGCATGTNATTGNGGGTNATGTNANNTNNNNTNNNNNNNN
    +
    !%(''(%%&/%%%%'&!)'+%!%&+1!%)'(!%!!(!!!!)!!!!!!!!
    @GO06_2500_Mate:1_5_104/2
    NGAAAGGAGGGAGAGGNAAGTNAGTTNAGGTNGNNTNNNNTNNNNNNNN
    +
    !'&(%(*0'&+&%+%%!%*)%!(+%(!'&%(!(!!'!!!!%!!!!!!!!
    @GO06_2500_Mate:1_9_50/2
    NAAATAAAAAGCCGGAAAAGTNGGGTNAATGNANNTNNNNANNNNNNNN
    +
    !%'*'%&&%(*%%)1(%)(**!%&),!)%%%!%!!%!!!!(!!!!!!!!

    can any body help me with this error i
    Last edited by huma Asif; 12-09-2014, 04:43 AM.

  • #2
    I copied your code and had a similar problem.
    But writing it in the same style, it worked:
    Your '-' symbols look on my bash a bit shorter than mine.
    Code:
     -v vs. ‐v
    Try to re-write your code in a plain text editor and run it again.

    Comment


    • #3
      i corrected that but now getting this error
      failed to open input file 'GO06_2500_Mate.read2.fastq': Value too large for defined data type

      Comment


      • #4
        How big is your file?
        Maybe it is really to big for the old fastx tool-kit.
        If that's the case and you need to stick to the program, you can split the file into several smaller ones.

        Alternatively, you may have a look at bbduk. Especially, if you are dealing with paired-end data.

        Comment


        • #5
          thank you for your help
          i will try that

          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...
            Yesterday, 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, 04-11-2024, 12:08 PM
          0 responses
          58 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-10-2024, 10:19 PM
          0 responses
          54 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-10-2024, 09:21 AM
          0 responses
          45 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-04-2024, 09:00 AM
          0 responses
          55 views
          0 likes
          Last Post seqadmin  
          Working...
          X