Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • cement_head
    Senior Member
    • Mar 2012
    • 265

    #1

    AlienTrimmer Question

    Hello,

    When using AlienTrimmer to trim PE data, it generates three files: R1 trimmed, R2 trimmed, and a "singles" file (one read failed the QC test). When you do a de novo assembly, does one use all three files? Or just the R1 / R2 PE files?

    Thanks,
    Andor
  • Brian Bushnell
    Super Moderator
    • Jan 2014
    • 2709

    #2
    Some assemblers can take both paired and unpaired reads at the same time, but if you have sufficient coverage with the paired reads only, I'd recommend throwing away the singletons. They add complexity and are likely to be lower quality anyway; for example, they may be reads that should have been removed (due to the presence of adapters or other non-genomic artifacts) but were not removed because they had so many errors it prevented detection.

    Comment

    • cement_head
      Senior Member
      • Mar 2012
      • 265

      #3
      Originally posted by Brian Bushnell View Post
      Some assemblers can take both paired and unpaired reads at the same time, but if you have sufficient coverage with the paired reads only, I'd recommend throwing away the singletons. They add complexity and are likely to be lower quality anyway; for example, they may be reads that should have been removed (due to the presence of adapters or other non-genomic artifacts) but were not removed because they had so many errors it prevented detection.
      Cheers - thanks - that was exactly the direction I was leaning.

      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...