Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • ddaneels
    Member
    • Mar 2012
    • 20

    #1

    Linux Command for joining left & right hand reads

    I know that there's a tool in Galaxy called 'Fastq Joiner' in which 2 fastq files (one with left & one with right hand reads) are joined together.
    Is there a simple Linux command to do the same thing? Something with the 'grep' command perhaps?
  • Heisman
    Senior Member
    • Dec 2010
    • 534

    #2
    I don't quite understand. Would the "cat" or "paste" command be sufficient?

    Comment

    • ddaneels
      Member
      • Mar 2012
      • 20

      #3
      Apologies, instead of 'grep' I meant 'paste'. Like you said I tried paste file1.fastq file2.fastq

      But I'm not sure that this command does the same as the 'fastq joiner' tool in Galaxy

      Comment

      • SeekAnswers
        Member
        • Mar 2012
        • 21

        #4
        You'd need a small perl script to read in the sequence identifiers to imitate the galaxy joiner. I don't think there's a simple linux command unless your files are both in the same order.

        Comment

        Latest Articles

        Collapse

        • SEQadmin2
          Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
          by SEQadmin2



          CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

          Despite this, “CRISPR helped turn genome editing from a specialized technique into
          ...
          07-31-2026, 11:01 AM
        • SEQadmin2
          Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
          by SEQadmin2


          Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

          The systematic characterization of the human proteome has
          ...
          07-20-2026, 11:48 AM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by SEQadmin2, 08-13-2026, 12:22 PM
        0 responses
        25 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 08-11-2026, 10:35 AM
        0 responses
        20 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 08-06-2026, 07:41 AM
        0 responses
        33 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 08-03-2026, 10:13 AM
        0 responses
        51 views
        0 reactions
        Last Post SEQadmin2  
        Working...